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<h3>Job Description</h3>
Job Description
Lantheus is headquartered in Bedford, Massachusetts with offices in New Jersey, Canada, and Sweden. For more than 60 years, Lantheus has been instrumental in pioneering the field of medical imaging and has helped physicians enhance patient care with its broad product portfolio. 
Lantheus is an entrepreneurial, agile, growing organization that provides innovative diagnostics, targeted therapeutics, and artificial intelligence (AI) solutions that empower clinicians to find, fight and follow disease. At Lantheus our purpose and values guide our behaviors in all interactions and play a vital role in creating a dynamic environment that contributes to our success. Every employee is crucial to our success; we respect one another and act as one knowing that someone’s health is in our hands. We believe in helping people be their best and are seeking to bring together a diverse group of individuals with different viewpoints and skill sets to be a part of a productive and inclusive team. 
Position Summary
Operates with a high degree of independence and is adept at conceptually outlining development, qualification, and life-cycle management studies with a focus on process analytical concepts to monitor and control critical steps in the manufacturing process of radiopharmaceuticals, ensuring consistent quality and safety meet current regulatory requirements on radiopharmaceutical drug products. Drives development and validation of new and improved radiochemical process controls in commercial processes; implements analytical methods and/or physicochemical characterizations in support of process development; radiolabeling processes and detection; and/or technology transfer to Contract Organizations. These efforts support the economical, efficient, and safe manufacture of radiolabeled precursors, bulk drug substances, and/or drug products. Lead PET CMO analytical operations and execution from late-stage development through site qualification. Engages in the development of complex strategies and testing requiring implementation of sophisticated, specialized scientific knowledge and advanced lab techniques, with latitude for independent judgment, decisions, and action. Radiopharmaceutical experience is preferred.
Essential Functions
<ul>
<li>Plans and drives multiple projects, requiring initiative and innovation, within Lantheus’ Quality system and governing regulations. Works on complex problems of diverse scope while serving as a technical analytical SME. Identifies, analyzes, and interprets project results. Evaluates results and examines implications to program.</li>
<li>Participate in technical troubleshooting sessions for processes and products manufactured in-house and at CMOs as needed and in investigating atypical/OOS results.</li>
<li>Performs routine laboratory, including working with radioactive materials, or oversees these actions at PET CMOs. Demonstrates ability to follow SOPs and Lantheus’ procedures as written. Tracks laboratory supplies and replenishes when needed. Maintains laboratory notebook, record keeping, and laboratory safety in accordance to common industry GLPs and Lantheus’, or CMO site, procedures.</li>
<li>Exhibits an increased understanding of radiochemistry, its regulations, stays aware of new scientific developments, and is able to incorporate these into their development/qualification activities.</li>
<li>Communicates scientific ideas and information in an appropriate and timely manner. Employs active listening skills to maintain clear communication to others. </li>
<li>Provides technical support to further program and Qualification activities at CMO/CROs; Authors technical transfer protocols and ensure acquired results are collected and documented according to cGMPs; Assists in completion of close-out reports and appropriate Change Controls. </li>
<li>Shows the ability and willingness to continually enhance functional and technical expertise. Assesses own strengths/ needs and learns from experience and feedback in order to continually enhance the level of functional and technical expertise. Takes action on developmental opportunities.</li>
<li>Accurately documents results in established formats. Able to write basic reports clearly and succinctly. Prepares written reports on all phases of laboratory and/or field experimental work. Presents results to colleagues at scientific meetings and to multidisciplinary audiences in program meetings. Writes comprehensive reports based on literature, lab and field data.</li>
<li>Maintains current knowledge of, and ensure all work activities are conducted in compliance with the full range of related internal and external systems, technology, regulatory requirements and related policies and procedures. Follows procedures to support intellectual property protection. May be responsible for preparing and defending patent disclosures and applications.</li>
<li>Actively promotes safety rules and awareness. Demonstrates good safety practices at all times including the appropriate use of protective equipment. Reports and takes initiative to correct safety &amp; environmental hazards.</li>
<li>Actively demonstrates the Lantheus values of Helping people be their best; Respect one another and act as one; Learn, adapt, and win; Know someone’s health is in our hands; and Own the solution and make it happen.</li>
</ul>
Typical Minimum Skills and Experience and Education 
<ul>
<li>Degree in Chemistry, Engineering, or related discipline or equivalent relevant industry experience.</li>
<li>Requires a minimum of a Ph.D. degree and 5+ years relevant industry work experience or a M.S. degree and 8+ years relevant work experience or a B.S. degree and 10+ years relevant industry work experience.</li>
<li>Scientific knowledge and experience in the technical aspects of radioanalytical chemistry and radiopharmaceutical process development and expertise in GMP documentation requirements with a working understanding of 21CFR 212 regulatory guidelines.</li>
<li>Previous experience working with radiopharmaceuticals and CMOs strongly preferred.</li>
</ul>
Other Requirements
<ul>
<li>Exceptional knowledge of scientific field of specialization. Familiar with Code of Federal Regulations parts 210 and 211 and supporting regulatory inspections.</li>
<li>Demonstrated skills in leading projects on an assigned team.</li>
<li>Able to properly handle and minimize exposure to potentially hazardous chemical, or radiological materials. Required to follow all safety procedures, and use personal and protective equipment provided.</li>
<li>Demonstrated competence in the design and documentation of complex experiments focused on a specific topic. Expanded scope to include multiple related questions for a given program.</li>
<li>Routine and or frequent lifting, with reasonable accommodations.</li>
<li>Demonstrated ability to effectively communicate ideas and information, both in oral and written form.</li>
<li>Travel (including international) is highly anticipated.</li>
</ul>
Lantheus is an equal opportunity employer that provides a workplace free from discrimination. All qualified applicants and employees are considered without regard to race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any other characteristic protected by law.
Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Lantheus Talent Acquisition team at <a href="mailto:talentacquisition@lantheus.com" target="_blank">talentacquisition@lantheus.com</a>.

Senior Scientist II PET Analytical Development

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
AbbVie (NYSE:ABBV) is a global, research-based biopharmaceutical company formed in 2013, following separation from Abbott. AbbVie combines the focus and passion of a leading-edge biotech with the expertise and capabilities of a long-established pharmaceutical leader, to develop and market advanced therapies that address some of the world's most complex and serious diseases.&nbsp; AbbVie employs approximately 50,000 people worldwide and markets medicines in more than 170 countries. Analytical Research and Development is seeking a Director (oral) Peptides to conduct process research and formulation development of parenteral and oral macrocyclic peptides from pre-clinical through early clinical phases.
Key Responsibilities:
<ul>
<li>The candidate will lead analytical teams associated with drug substance and drug product development and characterization of peptides and other modalities.
<ul>
<li>Leverage prior experience leading analytical efforts focused on phase appropriate peptide drug substance and drug product development.</li>
<li>Experience developing global regulatory strategies including authoring regulatory submissions, and responding to regulatory questions across global markets.</li>
<li>Lead across functions within project teams to deliver robust control strategies for starting materials, intermediates, drug substances and drug products.</li>
<li>Proactively drives innovation by leveraging external networks, industry insights, and prior experiences to identify emerging trends, foster strategic partnerships, and implement forward-thinking solutions.</li>
<li>Responsible for fit-for purpose method development, testing procedures, justifying specifications, and implementation of analytical control strategies to help the advancement of candidate molecules.</li>
<li>Proactively advise and share knowledge and expert opinions with subordinates, peers, and senior management.</li>
<li>Mentor and develop scientific staff in troubleshooting strategic and experimental issues and foster a culture of knowledge sharing.</li>
</ul>
</li>
<li>The position involves multi-disciplinary collaborations across Discovery, Development, Manufacturing, and Regulatory to execute and deliver material and information for clinical trials and regulatory submissions.&nbsp;</li>
<li>The candidate will identify and nurture ideas for continuous improvement activities and initiatives within the department.</li>
<li>This role may include management of direct reports.</li>
</ul>
Qualifications 
<ul>
<li>Bachelors, Masters, or PhD in Analytical Chemistry with a minimum of 18+ (B.S.), 16+ (M.S.), or 10+ (Ph.D.) years of related industry experience (advanced degree in Analytical Chemistry preferred)&nbsp;Experience with analytical aspects of advancing peptide modalities.</li>
<li>Proven scientific leadership; strong interpersonal and communication skills for facilitating collaborations and a demonstrated ability to represent analytical in cross-functional development teams.</li>
<li>In depth experience with analytical techniques required for peptide characterization, such as HPLC, SEC, chiral, amino acid analysis, peptide content, impurity identification, peptide mapping etc.</li>
<li>Demonstrated leadership of technical teams and effective cross-functional communication&nbsp;</li>
</ul>
<ul>
<li>Demonstrated capability to solve critical scientific and business problems&nbsp;</li>
</ul>
<ul>
<li>Demonstrated ability to implement and to grow the capabilities of an analytical organization and develop scientists into future leaders&nbsp;</li>
</ul>
<ul>
<li>Demonstrated experience with global regulatory expectations and regulatory filings in the peptide space.</li>
</ul>
Key AbbVie Competencies:
Interacts well with diverse groups within function and maintain strong working relationships with internal and external collaborators to enable higher performance.&nbsp;
<ul>
<li>Learns fast, grasps the "essence" and can change course quickly where indicated.</li>
<li>Raises the bar and is never satisfied with the status quo.</li>
<li>Creates a learning environment, open to suggestions and experimentation for improvement.</li>
<li>Embraces the ideas of others, nurtures innovation and manages innovation to reality.</li>
</ul>
Level and compensation will be commensurate with experience.
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future.​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;​
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Principal Research Scientist

<h3>Job Description</h3>
Job Description
Who We Are: 
At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented and diverse workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.
Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation. 
Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients. 
Role Overview:
The Scientist I - Process Research &amp; Development (PRD) is responsible for conducting small to large scale chemical reactions to optimize synthetic routes of active pharmaceutical ingredients (APIs) under the direction of project technical leads to deliver projects on target with quantity, quality, time, and within budget.
Core Responsibilities: 
<ul>
<li>Delivers experimental output with a high scientific integrity, both on time and target, and of high quality with guidance. </li>
<li>Exhibits safety awareness, safely conducts lab and other operations and hold themselves accountable for safe behavior in the work environment. </li>
<li>Maintains technical equipment and services.</li>
<li>Acts on feedback and show continuous commitment to learning and development.</li>
<li>Lead technical and operational areas and support troubleshooting for complex scientific issues under minimal guidance.</li>
<li>Expertly shares knowledge, skills and experience, communicating internally and externally. May lead focused projects as key contact. </li>
<li>Keeps accurate, legible and complete records of all experiments, observations, and equipment. </li>
<li>Writes high quality reports and delivers presentations to customers and management with some guidance in alignment with project milestones.</li>
<li>Contributes to sustaining good customer relations and identifies new commercial opportunities.</li>
<li>Actively contributes to the technical development of the department and company.</li>
<li>Accomplishes additional duties within the employee’s skills and abilities per reasonable request.</li>
</ul>
Qualifications: 
Required
<ul>
<li>PhD degree (or equivalent experience) in a chemistry related discipline.</li>
<li>2+ years hand on experience with PhD; 5+ years hand-on experience if Master's degree.</li>
<li>Proficiency with relevant lab and analytical techniques.</li>
<li>Previous industry experience in relevant areas.</li>
<li>Proficiency with relevant analytical techniques within an industry environment.</li>
<li>Ability to write clear and concise technical reports.</li>
<li>Good understanding of Microsoft Office and other relevant technical software platforms</li>
<li>Skilled in written and spoken communication and proven ability to effectively interact with management. </li>
<li>Demonstrates good judgment, quick decision-making skills, and the ability to work independently and in a team environment.</li>
</ul>
Physical Demands &amp; Work Environment:
<ul>
<li>Stand, walk, and manually operate objects, tools, or controls; reach with hands or arms; climb, balance, stoop, kneel, or crouch when necessary for the job activity.</li>
<li>Lift and/or move up to 50 pounds.</li>
<li>Specific vision abilities include near, distance, peripheral, color perception, and the ability to adjust focus.</li>
<li>Regularly work with moving mechanical parts and may work with toxic or caustic chemicals. </li>
<li>The work may be performed in humid areas with low or high temperatures. </li>
<li>This work may need to work with a respirator or operate with full-body Tyvek suits and supplied air or PAPR.</li>
</ul>
Our Commitment:
<ul>
<li>Health &amp; Wellness: Comprehensive health &amp; Wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies. </li>
<li>Financial Wellness: Comprehensive total compensation package that includes competitive base salary, Defined Contribution Pension program, eligibility for performance-based bonuses, and attractive 401(k) Plan with company match.</li>
<li>Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.</li>
<li>Inclusive Culture: At Veranova an inclusive culture is integral to our values. We are committed to ensuring that everyone can bring their full self to work and thrive in their career.</li>
</ul>
How to Apply: 
At Veranova, we are on a mission to meet people that believe in our values and can contribute to the team in a variety of ways. Please visit <a href="http://www.veranova.com" target="_blank">www.veranova.com</a> to view all open roles and join our Talent Community to stay connected and learn about opportunities as they arise. 
We value a range of experiences and perspectives. If you want to be part of improving and saving the lives of patients, we encourage you to apply regardless of whether you meet every qualification listed. 
If you are a veteran, first responder, or in the process of transitioning from service member to civilian life, we encourage you to apply. Your experience brings invaluable skills and insights that can contribute to our team.
For applicants who may require a reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email to <a href="mailto:talentacquisition@veranova.com" target="_blank">talentacquisition@veranova.com</a> in order to confirm your request for an accommodation. Please include the job number, title, and location of role. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Veranova employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Additional Information:
Applicants for this role must be authorized to work in the United States without further employer sponsorship.
Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting. 
Important Notice Regarding Recruitment Scams: Veranova is committed to providing a professional and secure recruitment experience for all applicants. Unfortunately, fraudulent job postings and recruitment scams are becoming more prevalent. We want to ensure that all candidates are aware of potential scams. Please see our notice here.
<ul>
<li>Legitimate communications from Veranova will only come from official email addresses using our domain: @veranova.com.</li>
<li>Legitimate LinkedIn communications will only come from active Veranova employees.</li>
<li>Veranova will never ask candidates for sensitive personal information during the application process (e.g., bank account details or social security number).</li>
<li>Veranova will never ask candidates for payment (e.g., for equipment, training, or background checks).</li>
</ul>
If you have any doubts or concerns about the authenticity of a job posting, please reach out to our HR department: <a href="mailto:pharm.hr@veranova.com" target="_blank">pharm.hr@veranova.com</a> (US) or <a href="mailto:UKHR@veranova.com" target="_blank">UKHR@veranova.com</a> (UK).
All your information will be kept confidential according to EEO guidelines.
Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.
All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.

Scientist - Process Research & Development

<h3>Job Description</h3>
Job Description
The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures. 
WORKING AT GENEZEN
Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team.
JOB SUMMARY
The Sr Scientist/Technical Lead Analytical Development will be part of the Process Development group, reporting to the Director of Process Development. He/She focuses on defining and managing the execution of the analytical development strategies and activities across the program/project lifecycle supporting process development and characterization. 
The Sr Scientist owns the analytical development assay lifecycle both from a technical and planning standpoint. Responsibilities will include scientific review and oversight of assay design, development, qualification, troubleshooting, and transfer as well as product characterization. The Sr Scientist will also be responsible for ensuring oversight of the analytical project timelines, and alignment across different teams and contributors to the analytical development efforts. The Sr Scientist is also responsible for management, training, and mentorship of junior Scientists and Associates within the Analytical Development team. 
ESSENTIAL JOB FUNCTIONS
The Sr. Scientist/Technical Lead will be a contributor to the activities of the Process Development group with specific attention toward the critical activities of the team: 
<ul>
<li>Developing, qualifying and transfer of client/product-specific assays to be used for in-process, release testing, and process characterization </li>
<li>Providing analytical support to Upstream and Downstream process development team activities by ensuring consistent and timely execution of standardized platform product characterization assays, including data review, storage and trending</li>
<li>Facilitating integration of new products into Genezen analytical platforms, to ensure timely progress of transfers and timelines</li>
<li>AD team leadership including training, development and mentoring</li>
<li>Owns the development lifecycle (method development, qualification, transfer), planning and timelines for multiple projects</li>
<li>Responsible for analytical strategy and timeline definition and monitoring in line with overall project timelines and functional team input</li>
<li>Oversees the project from an analytical standpoint as core member of the project team, and has key interactions with Upstream &amp; Downstream process development, supply chain, and external consultants and vendors</li>
<li>Communicates and aligns with internal and external stakeholders' activities relevant to specific projects planning and progression</li>
<li>Prepare data overviews and reports, including interpretation of results. Proposes next steps in experimental design including rational and timelines</li>
<li>Presents project updates, progress and results to internal and external stakeholders</li>
<li>Drafts or reviews laboratory and technical documentation such as SOPs, protocols, reports, position papers and memos</li>
<li>Assist team members with their planning and coordination of activities</li>
<li>Ensure all laboratory activities are performed according to applicable procedures to ensure a safe working environment and high data quality</li>
<li>Provide improvement suggestions and enforce improvement implementation </li>
</ul>
SPECIAL JOB REQUIREMENTS
<ul>
<li>Adaptability required as work schedule may change based on business needs</li>
<li>Criminal background check required</li>
<li>Other duties as assigned</li>
</ul>
KNOWLEDGE, SKILLS AND EXPERIENCE
EDUCATION / CERTIFICATIONS / LICENSES
Essential/Desired
MSc with 10+ years of industrial experience in a Life Sciences related field (biochemistry, molecular biology, biotechnology)
Essential
PhD with 6+ years of industrial experience in a Life Sciences related field (biochemistry, molecular biology, biotechnology)
Preferred
ON-THE-JOB EXPERIENCE

Broad knowledge of the pharmaceutical industry, including in depth operating knowledge of functions and assays relevant to viral vector therapeutic analytical within drug development processes
Essential
Demonstrated experience in project management skills and leadership experience, including setting timelines, alignment and helping others meet timelines
Essential
Prior managerial experience
Preferred
SKILLS / ABILITIES

Thorough scientific knowledge and hands-on experience with cell-based assays and bioassays, specifically in vitro potency assays
Essential
Thorough scientific knowledge and hands on experience with relevant molecular biology techniques (e.g. qPCR &amp; dPCR, DNA electrophoresis)
Essential
Thorough scientific knowledge and hands on experience with biochemical analyses (e.g. protein electrophoresis, western blotting, ELISA)
Essential
Thorough scientific knowledge in the process of assay design, assay development and trouble shooting
Essential
Experience in viral vaccines or gene therapy
Essential
PHYSICAL DEMANDS 
While performing the duties of this job, the employee is required to meet the following physical demands:
Work Environment
<ul>
<li>Frequently required to work in a BSL 2 environment with personal protective equipment/aseptic gowning</li>
<li>Regularly required to work around large machinery and typical utilities seen in pharmaceutical facilities</li>
<li>Occasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shock</li>
<li>Occasionally exposed to extremely loud noise levels</li>
<li>Spending time on the floor during activity execution (maintenance, construction, commissioning and qualification) is required</li>
</ul>
Movement
<ul>
<li> Frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms</li>
<li>Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl</li>
</ul>
Lifting
<ul>
<li>Frequently lift and/or move up to 10 pounds</li>
<li>Occasionally lift and/or move up to 25 pounds</li>
</ul>
Vision 
<ul>
<li>Frequently utilize close vision and the ability to adjust focus</li>
</ul>
Communication
<ul>
<li>Frequently required to communicate by talking, hearing, using telephone and e-mail</li>
</ul>
GENEZEN'S CURES VALUE-BASED COMPETENCIES
Committed to Science We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare.
Urgency in action for the patients We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs.
Resilience &amp; Grit in operations We are committed to overcoming challenges, learning from failures, and persistently striving for success. 
Execute with Excellence &amp; Integrity We are dedicated to delivering quality results and upholding ethical principals.
olutions driven for our partners We are committed to being a proactive, collaborative, creative and open-minded partner.
GENEZEN'S BENEFITS
<ul>
<li>Paid vacation days, amount based on tenure</li>
<li>Paid sick time</li>
<li>10 observed holidays + 2 floating holiday + 1 volunteer day</li>
<li>401(k) plan with company match up to 6% of salary, vested immediately</li>
<li>Share Appreciation Rights</li>
<li>Choice of several healthcare plans</li>
<li>FSA and HSA programs</li>
<li>Dental &amp; vision care</li>
<li>Employer-paid basic term life/personal accident insurance</li>
<li>Voluntary disability, universal life/personal accident insurance</li>
<li>Accidental Death &amp; Dismemberment (AD&amp;D) Insurance</li>
</ul>
ADDITIONAL DETAILS
<ul>
<li>Nothing in the job description for this role restricts management's right to assign or reassign duties and responsibilities to this job at any time.</li>
<li>This position requires a criminal background check.</li>
<li>Genezen is an Equal Opportunity Employer.</li>
<li>Genezen participates in EVerify.</li>
<li>Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas.</li>
</ul>
Genezen has operates two locations: one in Fishers, Indiana and the second in Lexington, Massachusetts. 
Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world's largest children's museum--to name just a few reasons why this area is a great place to live.
Lexington, Massachusetts, located just northwest of Boston, is renowned as a historic suburb with a rich cultural heritage. It boasts picturesque New England charm, tree-lined streets, and a vibrant community. Known for its pivotal role in the American Revolution, Lexington offers visitors and residents alike a blend of historical landmarks, modern amenities, and a strong sense of community pride.

Sr. Scientist - Analytical Development

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
The Bioinformatics for Immunology, Genetics, and Genomic Sciences group in the Genomics Research Center (GRC) at AbbVie is seeking a highly motivated and experienced AI/ML leader to transform our drug discovery and development through cutting-edge method and technology innovation. AbbVie’s GRC is a center of excellence for bioinformatics, functional genomics, human genetics, and pharmacogenomics. The GRC collaborates across R&amp;D, supporting both discovery research and clinical development, while integrating with process sciences, search and evaluation initiatives, and corporate strategic planning.
This position will be based in Cambridge, Massachusetts (hybrid). The candidate will lead a team of computational biologists and AI/ML experts focused on developing computational innovation to accelerate drug discovery and development across therapeutic and functional areas such as immunology, ophthalmology, aesthetics, specialty medicine, genetic medicine, process development, novel technologies, and human genetics. The successful applicant will identify opportunities and implement innovative solutions that address critical challenges in forward and reverse translation, biomarker discovery, mechanistic characterization, and therapeutic development optimization, while effectively communicating insights to key internal teams and external partners. In addition, the candidate will contribute to presentations at scientific conferences and publications of translational findings in peer reviewed journals, new drug applications and regulatory filings.
Key Responsibilities:
· Lead a diverse team of up to 10 FTEs specializing in computational method and novel technology innovation across AbbVie’s therapeutic and functional areas.
· Design and implement advanced AI/ML algorithms tailored to tackling complex problems across the drug development pipeline, including target discovery, translational research, biomarker development, patient stratification, therapeutic design, manufacturing science, and clinical trial optimization.
· Identify, evaluate, and implement emerging AI/ML methodologies, including state-of-the-art Generative AI, to deliver measurable impact on pipeline productivity and success.
· Act as the AI/ML expert in program teams, providing guidance and suggestions on cross-functional innovation projects.
· Develop and implement analytical approaches and best practices for novel technologies such as spatial transcriptomics, long-read sequencing, and CRISPR with strategic partners.
· Mentor leaders, emerging scientists and build capabilities, fostering an environment of scientific excellence and continuous growth.
· Communicate analytical approaches and results effectively to scientific and technical audiences.
· Provide expertise and technical consultation for external collaborations/partnerships in academia and industry.
Qualifications 
Basic Qualifications:&nbsp;
· PhD. in bioinformatics, statistics, mathematics, computer science, computational biology, genomics, or a related field with 8+ years industry/academic experience.
· Or master’s degree with 15+ years of relevant experience.
· 3+ years of experience managing direct reports.
· 5+ years of hands-on experience in analyzing and integrating multi-omics data (e.g., bulk and single-cell RNA-seq, proteomics, genetics, epigenetics data).
· 3+ years of hands-on experience developing novel methods including AI and ML approaches.
· Highly proficient with statistical and programing languages (R, Python), Unix/Linux and cloud computing environment.
Preferred Qualifications:
· At least 3 years of experience managing teams, including managing managers with direct reports, and setting strategic goals for their teams within a highly matrixed organization.
· Deep understanding of human disease biology across various therapeutic areas such as immunology, aesthetics, and ophthalmology.
· Experience applying advanced computational modeling and AI/ML approaches to optimize therapeutic protein design, enhance production efficiency, and accelerate genetic medicine development.
· Expertise in predictive modeling, quantitative data analysis, and novel method development leveraging multi-modal preclinical, clinical, and real-world data.
· Experience with optimizing and fine-tuning foundation models, and applying LLM, Generative AI, and Agentic AI frameworks to biological questions.
· Experience with multi-omics data integration and with novel technologies such as spatial transcriptomics, Perturb-seq, CRISPR, long-read sequencing, etc.
· Demonstrate strong communication skills that allow you to effectively communicate complex technical concepts to diverse audiences and scientific leadership.
· Collaborative and self-motivated, able to manage multiple objectives and adapt to changing priorities.
· Strong track record of publications and/or patents in this space.
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future.​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
​
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;​
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Principal Research Scientist, Method and Technology Advancements Lead

<h3>Job Description</h3>
Job Description
About Seismic
Seismic Therapeutic, a cutting-edge biomedicines company at the intersection of machine learning, protein engineering, and immunology, is seeking a creative, independently-minded machine learning scientist to help accelerate the Impact Platform for the computational discovery and optimization of new biologic drugs. Seismic’s machine learning platform enables on-demand generation and optimization of protein therapeutics to fight diseases of the immune system, using the power of artificial intelligence to translate audacious ideas into breakthrough drugs. Weare dedicated to building a supportive culture around a superstar team, while keeping the unmet needs of patients at the center of our goals. Seismic has the tools, skills, ideas and people to make this vision a reality. 
Working closely with our team of machine learning scientists, structural biologists, immunologists and others, you will develop and apply innovative machine learning approaches to optimize natural proteins for clinical applications and design novel classes of synthetic proteins with therapeutic functions. 
Who you are and what you bring:
<ul>
<li>A rigorous machine learning scientist with a deep understanding of molecular biology, protein biochemistry and structure.</li>
<li>Appreciation of the characteristics that make a robust biologic drug.</li>
<li>Hands-on experience with protein design models incorporating sequence (evolutionary sequence models and large language models) and/or structure (diffusion and inverse folding models).</li>
<li>Ability to communicate complex machine learning and computational concepts to audiences with a wide range of backgrounds and technical familiarity.</li>
<li>Experience working with wet lab teams to bridge the divide from in-silico designs to real-world applications.</li>
<li>Driven and conscientious, thriving in a fast-paced, entrepreneurial environment.</li>
<li>Passionate about improving patients’ lives.</li>
</ul>
Core Responsibilities:
<ul>
<li>Design and train new classes of machine learning models to optimize natural proteins for therapeutic properties and design synthetic proteins with novel therapeutic functions.</li>
<li>Spearhead computational de novo antibody design efforts to create new therapeutics targeting challenging antigens. </li>
<li>Integrate diverse external and internal data sources including protein sequence, structure, function, and molecular characterization data to enable detailed modulation and multi-objective optimization of protein properties.</li>
<li>Work with a diverse team of protein scientists, immunologists, and clinical experts to tailor modeling efforts toward high-impact therapeutic applications.</li>
<li>Establish robust data infrastructure to enable machine learning model training and deployment of data analysis and visualization tools. </li>
<li>Develop production-quality code in a team setting for use by both computational and wet-lab scientists. </li>
<li>Present progress from scientific work in regular meetings and prepare reports and slide decks for broader internal and external communication.</li>
</ul>
Required Qualifications:
<ul>
<li>PhD in Mathematics, Computational Biology, Computer Science, Statistics or a related field. Exceptional candidates with extensive computational experience and a PhD in a non-computational field will also be considered. </li>
<li>3+ years of industry experience with developing and applying machine learning methods to create new biological drugs, using deep learning models such as variational autoencoders and graph neural networks. </li>
<li>Application of ML in the field of drug discovery is essential with hands-on experience in the following: protein engineering, or statistical genetics are especially relevant. </li>
<li>Demonstrated experience collaborating with wet lab scientists to generate and analyze real-world data in an applied setting, especially in the context of pharmaceutical development. </li>
<li>Proficiency in Python and data analysis with Numpy/Scipy, R, or another statistical programming language.</li>
<li>A strong drive to collaborate and communicate with a diverse and vibrant team of both dry and wet lab scientists. </li>
</ul>
It's a plus but not required:
<ul>
<li>Experience with AWS, Google Cloud, or another cloud computing framework. </li>
<li>Familiarity with Dash, R Shiny, or another interactive app development framework.</li>
<li>Application of ML in the fields of genomics and immunology.</li>
<li>Publications in major scientific journals that apply machine learning methods to problems in molecular or structural biology.</li>
</ul>
 
As a member of our diverse and growing team, you’ll help shape Seismic into a company that takes its scientific mission seriously while providing a positive and supportive workplace environment and culture. With your insights, passion, and talent - we’ll bring novel therapeutics to the patients who need them the most.
Seismic Therapeutic is an equal opportunity employer. We will not tolerate discrimination on the basis of race, color, national origin, sex, sexual orientation, gender identity, religion, age, disability, veteran's status, pregnancy, genetic information or on any basis prohibited by federal, state or local law.

Scientist / Senior Scientist, Machine Learning

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
The Senior Scientist I will be an integral part of the Analytical Development team in the Operations – Product Development Science and Technology – Biologics division. The role involves managing all analytical aspects of biologics products at different stages of their drug development lifecycle with a focus on advancing AbbVie’s pre-clinical and early clinical programs. The individual will play a key role in analytical method development, method transfer, troubleshooting, specification setting and justification, stability studies, and regulatory filings. Collaboration with other analytical teams, quality control, bioprocess development, and R&amp;D groups is a crucial part of this role to meet business objectives and program milestones.
Responsibilities:
<ul>
<li>Execute and/or lead method development and analytical testing to support pipeline programs using analytical separation techniques including HPLC/UPLC, electrophoresis, etc.</li>
<li>May initiate new areas of investigation that are scientifically meaningful, reliable, and can be incorporated directly into a research or development program. Demonstrates high proficiency across a wide range of relevant technologies.</li>
<li>Partner with other groups in the Analytical Development team to provide analytical support for pipeline programs using traditional and advanced analytical techniques, including but not limited to ELISA, bioassays, mass spectrometry, biophysical, spectrophotometric and compendial methods.</li>
<li>Participate in cross-functional, multi-site meetings / projects and coordinate analytical activities that need to be supported in the Analytical Development team for pipeline programs.</li>
<li>Participate in the preparation and review of internal technical documents to ensure compliance.</li>
<li>Author regulatory submissions and provide scientifically sound responses to agency deficiency letters.</li>
<li>Evaluate and implement novel analytical techniques to expand analytical capabilities in the Analytical Development team</li>
<li>Mentor or supervise junior members in the same team.&nbsp;</li>
</ul>
Qualifications 
<ul>
<li>PhD in Chemistry, biochemistry, biological sciences, chemical engineering or related scientific disciplines with 0-2 years relevant experience, or MS or BS with 9-12+ years relevant experience</li>
<li>Proficient in the characterization of proteins, mRNA, DNA, or various other modalities</li>
<li>Experience in analytical method development, validation, and transfer in support of biological products is preferred. &nbsp; Methods including but not limited to HPLC/UPLC, capillary electrophoresis, spectrophotometry, mass spectrometry, biophysical methods, ELISA and bioassays.</li>
<li>Ability to think critically and demonstrate troubleshooting and problem-solving skills.</li>
<li>Ability to lead and manage projects of significant scope and complexity, while meeting all deliverables and timelines.</li>
<li>Ability to effectively communicate with stakeholders and collaborate with cross-team partners.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future. ​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;​
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Senior Scientist, I

<h3>Job Description</h3>
Job Description
Location: Manchester, NH
Job Type: Full-time
Job Title: Senior Lab Personnel Specialist - PCR &amp; NGS
Salary: $110,00 - $140,000 annually
Shift: Day, Monday - Friday
About the Role:
We are seeking a driven, experienced, and detail-oriented Senior Lab Personnel Specialist to join our innovative genetics lab team. Our lab is dedicated to accelerating the diagnosis of numerous genetic diseases through leading-edge genetic sequencing technologies. In this key role, you will provide advanced technical expertise and mentorship across cutting-edge projects involving PCR and Next Generation Sequencing (NGS). You will help lead lab operations, balancing the execution of CLIA-validated tests for routine diagnostic workflows with the development and optimization of new sequencing technologies and molecular assays that drive our mission forward. Tasks will include a combination of hands-on assay execution and technician supervision, all while demonstrating a devotion to total quality and continuous improvement.
Key Responsibilities:
- Perform, oversee, and troubleshoot complex molecular workflows for both diagnostic and research projects, including PCR assay design, optimization, validation, and routine testing, with a mix of hands-on execution and supervision of lab technicians.
- Conduct and supervise Next Generation Sequencing (NGS) sample preparation, library construction, sequencing runs, and data analysis, ensuring seamless integration between CLIA-validated diagnostic tests and innovative technology development while directly executing assays and guiding team members.
- Act as a technical lead and resource for troubleshooting PCR and NGS protocols, instrumentation, software tools, and bioinformatics pipelines.
- Train and mentor lab personnel on advanced molecular techniques, experimental design, SOPs, best practices, and emerging genetic sequencing technologies, including direct supervision during hands-on assay performance.
- Support cross-functional teams by providing input on experimental design, assay development, data interpretation, and the execution of CLIA-validated tests to ensure accurate and timely genetic disease diagnoses.
- Review, analyze, and interpret sequencing results to guarantee accuracy, validity, and compliance with regulatory standards.
- Draft, review, and update SOPs, work instructions, and protocols in line with internal quality standards, industry best practices, and regulatory requirements (e.g., CLIA, CAP), emphasizing continuous improvement and total quality management.
- Ensure rigorous quality control, compliance with lab safety, research integrity guidelines, and GLP in a combined diagnostic and R&amp;D setting, with a commitment to ongoing process enhancements.
- Collaborate with scientists, bioinformaticians, and project managers to meet timelines, share findings, drive innovation, and accelerate genetic disease diagnostics.
- Maintain and troubleshoot lab instrumentation, ensuring calibration, preventative maintenance, and proper documentation.
- Contribute to process improvements, new method development, and continuous learning within the lab team, with a focus on advancing sequencing technologies for genetic applications and upholding devotion to total quality.
-Ensuring the laboratory takes remedial action when test systems deviate from the laboratory's established performance specifications
- Assuring patient test results aren't reported until all corrective actions have been taken and the test system functions properly
- Making sure that all testing personnel receive orientation and training.
- Evaluating and documenting the competency of all testing personnel
Qualifications:
- Bachelor's degree in Molecular Biology, Genetics, Biotechnology, or a related life sciences field required; Master's degree preferred.
- Certification as a Molecular Biology Technologist (MB) or equivalent (ASCP or similar) strongly preferred.
- 4+ years of hands-on experience in a molecular biology lab environment, with significant expertise in PCR and NGS workflows, including both R&amp;D and diagnostic settings.
- Direct experience working with NGS platforms (e.g., Illumina, Oxford Nanopore, PacBio, or Thermo Fisher) and associated bioinformatics tools and pipelines.
- Strong grasp of molecular assay development, troubleshooting, optimization, validation processes, and the execution of CLIA-validated tests.
- Familiarity with data analysis software, bioinformatics for NGS data, and regulatory guidelines (e.g., CLIA, CAP) is highly desirable.
- Proven leadership and training abilities with strong communication, collaborative, and problem-solving skills, including experience in technician supervision.
- Demonstrated ability to work independently, manage multiple projects simultaneously, and adapt to evolving priorities in a fast-paced genetics lab.
- Knowledge of good laboratory practices (GLP), research integrity standards, and lab safety requirements.
Why Join Us:
- Be part of a dynamic and collaborative genetics lab environment tackling challenging and impactful questions in genetic disease diagnosis, with a strong devotion to total quality and continuous improvement.
- Work with state-of-the-art molecular technologies and contribute to the development of innovative sequencing solutions that accelerate diagnoses.
- Competitive salary and comprehensive benefits package.
- Ample opportunities for growth, skill development, scientific contribution, and professional advancement.
About us:
At Lighthouse Lab Services, we offer solutions to help start, grow, and run clinical laboratories. Our recruiting team has over 18 years of proven success placing job seekers in positions ranging from entry-level Medical Technologists to seasoned Laboratory Directors. We recruit nationwide, for permanent and travel positions with clients ranging from small hospitals to large reference laboratories.
It is the policy of Lighthouse Lab Services to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. Lighthouse Lab Services is committed to working and providing reasonable accommodation to individuals of all abilities, including persons with disabilities.
If at any time during the application process, you need an accommodation, please contact <a href="mailto:recruiting@lighthouselabservices.com" target="_blank">recruiting@lighthouselabservices.com</a> for assistance.
Lighthouse Lab Services | 844-974-1929 | lighthouselabservices.com
#LLS2

?Senior Lab Personnel Specialist - PCR & NGS

<h3>Job Description</h3>
Job Description
Who We Are: 
At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented and diverse workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.
Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation. 
Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients. 
Role Overview:
We are seeking a highly motivated and skilled Senior Scientist with experience in analyzing antibody drug conjugates (ADC) to join our ARD team in New England. The successful candidate will play a hands-on role in the development, qualification, transfer, and validation of analytical methods to support the development of ADC’s and other complex bioconjugates. 
Core Responsibilities: 
<ul>
<li>Collaborate with cross-functional teams to drive impactful projects. </li>
<li>Exercise technical judgment in the planning, implementation, and analysis of experiments related to method development, validation, reference standard creation and qualification, forced degradation, product characterization, and compatibility studies in accordance with pertinent ICH regulatory guidelines.</li>
<li>Perform method development, characterization, validation and analysis of bioconjugates including DAR (drug antibody ratio), DAR conjugation site occupancy, charge and size variants, purity, potency, free antibody and free linker payload using techniques such as HPLC, mass spectrometry, icIEF, SEC, CE-SDS, ELISA, Western Blot and UV-VIS spectrophotometry.</li>
<li>Author test methods, protocols, reports, and regulatory documents as needed.</li>
<li>Provide support for development and cGMP manufacturing campaigns, ensuring compliance with regulatory requirements and documentation standards - including both in-process and release samples.</li>
<li>Adhere to safety and quality standards. </li>
<li>Communicate technical findings and results to both internal and external stakeholders, including clients and regulatory bodies.</li>
<li>Well organized with good problem-solving skills, a high level of attention to detail and have a passion for delivering high quality data in a fast-paced environment.</li>
<li>Collaborate with chemistry development scientists, quality control and regulatory affairs teams to ensure successful project delivery.</li>
<li>Mentor and develop scientific staff. Ensure continued technical and professional growth of department members, encourage efforts towards excellence and knowledge sharing.</li>
<li>Possess strong communication (oral, written), organizational, and leadership skills</li>
</ul>
Qualifications: 
Required
<ul>
<li>Ph.D., M.S., or B.S. in Analytical Chemistry, Biochemistry, Chemistry, Chemical/Biomedical Engineering, or other related scientific discipline.</li>
<li>Relevant experience in analytical method development, validation and characterization of bioconjugates. (PhD with 4+ years, MS with 8+ years, BS with 10 + years of experience)</li>
<li>Hands on experience with various techniques used in the characterization of ADC’s such as HPLC, mass spectrometry, icIEF, SEC, CE-SDS, Western Blot, UV-VIS spectrophotometry, etc. </li>
<li>Knowledge with cGMP, GLP, and regulatory guidelines for bioconjugate development.</li>
<li>Demonstrates good judgment, decision-making skills, and the ability to work both independently and in a team environment.</li>
<li>Skilled in technical writing.</li>
<li>Experience in mentoring staff in the analytical department.</li>
<li>Strong communication and teamwork skills in a cross-functional environment.</li>
</ul>
Our Commitment:
<ul>
<li>Health &amp; Wellness: Comprehensive health &amp; Wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies. </li>
<li>Financial Wellness: Comprehensive total compensation package that includes competitive base salary, Defined Contribution Pension program, eligibility for performance-based bonuses, and attractive 401(k) Plan with company match.</li>
<li>Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.</li>
<li>Inclusive Culture: At Veranova an inclusive culture is integral to our values. We are committed to ensuring that everyone can bring their full self to work and thrive in their career.</li>
</ul>
How to Apply: 
At Veranova, we are on a mission to meet people that believe in our values and can contribute to the team in a variety of ways. Please visit <a href="http://www.veranova.com" target="_blank">www.veranova.com</a> to view all open roles and join our Talent Community to stay connected and learn about opportunities as they arise. 
We value a range of experiences and perspectives. If you want to be part of improving and saving the lives of patients, we encourage you to apply regardless of whether you meet every qualification listed. 
If you are a veteran, first responder, or in the process of transitioning from service member to civilian life, we encourage you to apply. Your experience brings invaluable skills and insights that can contribute to our team.
For applicants who may require a reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email to <a href="mailto:talentacquisition@veranova.com" target="_blank">talentacquisition@veranova.com</a> in order to confirm your request for an accommodation. Please include the job number, title, and location of role. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Veranova employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Additional Information:
Applicants for this role must be authorized to work in the United States without further employer sponsorship.
Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting. 
Important Notice Regarding Recruitment Scams: Veranova is committed to providing a professional and secure recruitment experience for all applicants. Unfortunately, fraudulent job postings and recruitment scams are becoming more prevalent. We want to ensure that all candidates are aware of potential scams. Please see our notice here.
<ul>
<li>Legitimate communications from Veranova will only come from official email addresses using our domain: @veranova.com.</li>
<li>Legitimate LinkedIn communications will only come from active Veranova employees.</li>
<li>Veranova will never ask candidates for sensitive personal information during the application process (e.g., bank account details or social security number).</li>
<li>Veranova will never ask candidates for payment (e.g., for equipment, training, or background checks).</li>
</ul>
If you have any doubts or concerns about the authenticity of a job posting, please reach out to our HR department: <a href="mailto:pharm.hr@veranova.com" target="_blank">pharm.hr@veranova.com</a> (US) or <a href="mailto:UKHR@veranova.com" target="_blank">UKHR@veranova.com</a> (UK).
All your information will be kept confidential according to EEO guidelines.
Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.
All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.

Senior Scientist - Analytical R&D - Antibody Drug Conjugates

<h3>Job Description</h3>
Job DescriptionSalary: 
ABOUT EPSILON
Epsilon Associates, Inc. is a leading engineering and environmental consulting firm with extensive experience in assisting clients with historic preservation planning, regulatory compliance and state and federal historic rehabilitation tax credits.
 
POSITION SUMMARY
Epsilon is seeking a full-time Preservation Planner/Architectural Historian to work with our expanding historic preservation group. Key responsibilities include preparation of documents and reports for submission to local, state, and federal government review agencies; including National Register eligibility evaluations and nominations, Project Notification Forms, historic property surveys, design review applications, archival photographic documentation, and state and federal historic rehabilitation tax credit applications.
 
PREFERRED QUALIFICATIONS AND REQUIREMENTS
The successful candidate will have a minimum BA/BS degree in Architectural History, Historic Preservation Planning, or closely related discipline (MA/MS is preferred) and will have 4-6 years of professional experience and must meet the Secretary of the Interiors professional qualifications.
 
Excellent research, writing, editing, and photographic abilities are required. Experience with building research, knowledge of architectural styles and forms, and periods of development and architectural history of New England as well as knowledge and experience with application of the Secretary of the Interiors Standards for the Treatment of Historic Properties is a must. Documented experience with the preparation of historic rehabilitation tax credit applications and National Register nominations is essential.
 
Fluency in reading architectural drawings and the ability to use computer hardware, software, and other related information technologies (Microsoft Word, Excel, PowerPoint, Adobe Acrobat, etc.) is required. Personal vehicle and a willingness to travel, primarily within Massachusetts and New England, also required.
 
Experience with federal and state cultural resource management with a working command of federal and state cultural resource and historic preservation statutes and regulations, including Section 106 and National Register criteria; knowledge of relevant Massachusetts regulations (Chapter 254 and MEPA) is a plus.
 
The ideal candidate will be detail oriented, have a professional demeanor and strong organizational skills, and possess the ability to manage priorities, meet deadlines, and multitask in a fast-paced environment. The candidate should be able to work in a team environment with a variety of project members and manage tasks as delegated by project lead. The candidate must possess strong communication skills including writing skills and the ability to work closely with clients. 
PHYSICAL REQUIREMENTS FOR THE JOB
The Candidate must:
<ul>
<li>be able to work on a computer for extended periods of time; and</li>
<li>be able to travel via car for an extended period of time.</li>
</ul>
 
SALARY RANGE
Epsilon offers competitive salaries commensurate with individual qualifications and experience and a full package of benefits. We seek motivated self-starters who are willing to work hard, communicate well, and have fun in a professional setting.
 
WORKING CONDITIONS IN WHICH THE DUTIES ARE PERFORMED
Epsilon maintains a professional office located in a historic mill in Maynard, MA. Office space is recently renovated, clean, quiet, and friendly. Company employees are currently working on a hybrid basis, which is well supported by company technology and infrastructure. Employees should plan to be in the Maynard office a minimum of 1-2 days per week with additional in-office time as needed for staff events, client meetings, and/or workload requirements.
Our team members enjoy regular opportunities for professional growth, a relaxed and flexible work environment, a competitive base salary, a 401k plan with a generous company match, profit sharing, an annual performance bonus program, and a full benefits package.
 
Epsilon is an equal opportunity employer that recognizes the value of a diverse workforce. We ensure a workplace that supports and encourages creativity, professional growth and a company culture that promotes diversity, inclusion and overall employee health and well-being. All qualified individuals will receive consideration for employment without regard to race, color, age, religion, gender, national origin, sexual orientation, gender identity, disability and/or protected veteran status in accordance with governing laws.
Epsilon Associates, Inc. is an EEO/Disability/Vets Employer
Applicants must have all necessary paperwork to work in the USA.

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