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<h3>Job Description</h3>
Job Description
About TEAM LEWIS
TEAM LEWIS is a global marketing agency that has grown from start-up to multi-national in a little over two decades. Its success is due to a combination of factors: talented creatives delivering award winning campaigns; expanding client relationships into new markets or services; its independence from outside investors. The agency, its people and client campaigns have won many awards, including Cannes Lions, PRovoke Media, ICCO, European Excellence, PRCA Digital, Digital Impact, Global Digital Excellence.
At the heart of the business is the TEAM LEWIS Foundation (TLF), a non-profit charitable entity. Since its launch in 2021, it has funded over 2,700 causes. The TLF promotes a wide variety of social, cultural, and environmental causes that benefit society. It aims to strengthen the bonds between the creative industries, businesses, government, and non-profits. Community charities are championed by employees who, in addition to the financial donation, volunteer their time and skills to maximize the grants’ effectiveness.
Purpose of the role TEAM LEWIS is seeking a Jr. Research Analyst to join its market research team. The team creates market research for public and private companies to help create gated content, generate media interest, assist with strategic planning or for better brand understanding. The selected individual will have the opportunity to help create meaningful PR measurement metrics for clients and to work on all phases of research projects. 
Key responsibilities and tasks 
<ul>
<li>Work with various data sources to create measurement metrics for PR, social and digital campaigns </li>
<li>Serve in a client facing role for measurement engagements </li>
<li>Ability to perform secondary research of various industries</li>
<li>Assist client teams as they work with clients to create market research for campaigns </li>
<li>Provide project management for market research projects </li>
<li>Assist with creating survey questionnaires </li>
<li>Create analysis plans </li>
<li>Generate charts and graphs that will be used within market research reports </li>
<li>Assist in creating market research reports </li>
<li>Program online surveys and assist in conducting focus groups </li>
</ul>
 About you 
<ul>
<li>Bachelor’s degree from an accredited university with a concentration in Management, Mathematics, Marketing, Economics or Statistics </li>
<li>1-2+ years of market research experience required </li>
<li>Advanced proficiency with Microsoft Office Suite (Excel, Word, PowerPoint, Access) </li>
<li>Knowledge of current media analysis tools (Meltwater, Traackr, Cision, etc.) </li>
<li>Knowledge and proficiency of statistical software package (R, SPSS, Decipher, etc.) </li>
<li>Experience with dashboard and/or visualization software (such as Tableau) </li>
<li>Ability to provide project management for internal market research projects </li>
<li>Experience writing survey questionnaires </li>
<li>Experience programming online surveys </li>
<li>Experience writing market research reports </li>
<li>Strong interpersonal skills and the ability to work within a cross functional environment </li>
<li>An entrepreneurial spirit, who can work with minimum direction </li>
</ul>
 
The expected salary range for the Research Analyst position is between $50K - $65K. Base annual salary is determined by factors such as location, experience, and expertise. 
We provide equal employment opportunities to all employees and applicants for employment and prohibit discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, reproductive health decisions and family responsibilities, qualifying acts of violence, or any other characteristic protected by federal, state or local laws.

Research Analyst

<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.
Biotherapeutics and Genetic Medicine (BGM), a part of Discovery Research within AbbVie’s R&amp;D, is a global organization that is responsible for discovering and optimizing drug candidate molecules for biotherapeutic modalities (monoclonal antibodies, multispecifics, proteins, conjugates, etc.) and genetic medicines (AAV, LNPs, siRNA etc.) for all therapeutic areas across discovery.
Job Description 
The Associate Director of Biotherapeutics &amp; Genetic Medicine (BGM) AI/ML partnerships will be a key leader in driving AbbVie's AI/ML external strategy. This role requires an energetic strategic thinker, attuned to the innovation landscape, with deep, technical AI/ML experience in biopharma, who can leverage their background to represent BGM’s strategic priorities in external engagements.
This position reports to the Head of AI/ML in BGM and will serve as a trusted advisor to senior leadership. This role is pivotal in driving our organization towards becoming a leader in the application of AI/ML, ensuring that AI/ML initiatives align with our overarching business objectives, delivering tangible business value and accelerating our promise to patients.
Key Responsibilities:
<ul>
<li>Develop a deep understanding of AbbVie’s biotherapeutics discovery processes and drug program pipeline and use that as a foundation to co-develop and champion an external AI/ML strategy that is aligned with key areas of impact, over both long- and short-term horizons.</li>
<li>Stay at the forefront of AI/ML innovation, technologies, and best practices, developing a bimonthly competitive intelligence report, in coordination with other teams that develop competitive intelligence across AbbVie, e.g., AI Strategy &amp; Partnerships, Commercial Digital, R&amp;D, BTS, and Corporate Strategy.</li>
<li>Collaborate with BGM’s internal AI/ML innovation team to conduct technical due diligence and detailed benchmarking of external partner AI/ML platforms with applicability to AbbVie’s BGM strategy.</li>
<li>Collaborate across the company (including Technology Licensing &amp; Collaboration, Search &amp; Evaluation, Business Development &amp; Acquisitions, etc.) to ensure collaboration agreements are aligned with the value proposition for BGM.</li>
<li>Manage and coordinate collaborations with external partners, document key activities and drive projects towards impact.</li>
<li>Communicate the impact of AI/ML partnerships to AbbVie’s pipeline both internally at governance bodies and, where appropriate, externally, to the AI/ML community through conference presentations.</li>
<li>Mentor leaders and team members, creating a pipeline of AI/ML champions.</li>
</ul>
Qualifications 
<ul>
<li>BS, MS, or PhD in&nbsp;Computational Chemistry, Bioinformatics, Computational Biology, Biology, or related discipline with typically 16+ (BS) years, 14+ (MS) years, or 8+ (PhD) years of &nbsp;experience.</li>
<li>Demonstrated ability to work cross-functionally with senior leaders and build trust-based partnerships to deliver results and influence change.</li>
<li>Experience with deep technical diligence on machine learning capabilities.</li>
<li>Prior experience in external partnerships and competitive landscape at a major pharma company or biotechnology organization.</li>
<li>Strong problem-solving mindset and comfort and ability to create structure from ambiguity.</li>
<li>Excellent executive communication and stakeholder-management skills with a proven ability to bridge technical and business perspectives.</li>
<li>Hiring, people management, and career development experience.</li>
</ul>
This position is located at one of our offices in Worcester, MA, Cambridge, MA, or San Francisco, CA. We offer flexible work arrangements, allowing you to choose between a fully on-site schedule or a hybrid model, which includes three days per week in the office.
 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>

Principal Research Scientist II - AI/ML Partnerships, Biotherapeutics and Genetic Medicine

<h3>Job Description</h3>
Job DescriptionCompany Description 
Canam Bridges designs, manufactures and installs steel bridges for major infrastructure contractors across North America. Canam Bridges is a member of Canam Group, which has over 5,100 employees and operates 22 plants in North America, as well as engineering offices in Canada, Romania, India and the Philippines.
Job Description 
Your life at Canam Bridges As a Metrologist at Canam Bridges, you will be responsible for taking factory measurements using “Station Total” and “Laser Tracker Faro” surveying tools. Your analytical mind will allow you to use your 3D vision superpowers to complete dimensional measurements. To break your routine, you will alternate between taking factory measurements, recording data, and writing reports. Your computer knowledge will make you an expert in AutoCAD and Polyworks. That said, it is your team that will give you the most satisfaction, because at Canam Bridges, we are a solid combination of expertise and pride!
Job Description Assist Plant Manager and production staff in developing production plans, ensure production objectives are met, offer recommendations, and implement production events and programs. The Metrologist is responsible for performing such work consistent with the company’s corporate mission, values, and departmental financial objectives.
Essential Functions
<ul>
<li>Assist in the production-planning process, schedules, assignments, and&nbsp;production sequences to meet production goals.</li>
<li>Read and analyze data, production schedules, and other records and reports to determine production productivity and to evaluate current production estimates and outputs.</li>
<li>Identify direct and indirect labor issues and production problems, make recommendations, and assist management in developing a corrective action plan.</li>
<li>Compile production planning notes, sketches, prints, schedules, contract documents and specifications into a formal build plan.</li>
<li>Aid in the detailing and manipulation of models to accommodate additional views for fabrication per planning session. Assist on designing fixtures and jigs to aid fabrication.</li>
<li>Responsible for conventional and CNC machining, to include managing direct labor to accomplish coverage on equipment in support of production needs.</li>
<li>Train and assist production members in the operation of conventional and CNC machining equipment in line with formal build plans.</li>
<li>Perform other job duties as assigned by the Plant Manager.</li>
</ul>
Qualifications 
<ul>
<li>Associate’s degree (A. A.) or equivalent from two-year college or technical school and/or experience in detailing and fabrication.</li>
<li>Must be able to use logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to production or productivity problems.</li>
<li>Experience with AutoCAD, Tekla, FeatureCam, Polyworks, Station Total, Laser Tracker Faro, and other software preferred.</li>
<li>Ability to communicate information and ideas in speaking, so others will understand.</li>
<li>Analyze information and evaluate results to choose the best solution and solve problems.</li>
<li>Must be able to schedule events, programs, and activities, as well as the work of others.</li>
<li>Job requires a willingness to lead, take charge, and offer opinions and direction.</li>
</ul>
 Additional Information 
Work Environment General office and production environment. Daily exposure to computer display and shop environment.&nbsp;&nbsp;
Remuneration We offer a competitive compensation and benefits package, as well as excellent opportunities for training and advancement.
Canam&nbsp;is an Equal Opportunity/Affirmative Action employer.&nbsp;All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.
If you need a reasonable accommodation for any part of the employment process, please&nbsp;contact us&nbsp;and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to.

Metrology Technician

<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.
Biotherapeutics and Genetic Medicine (BGM), a part of Discovery Research within AbbVie’s R&amp;D, is a global organization that is responsible for discovering and optimizing drug candidate molecules for biotherapeutic modalities (monoclonal antibodies, multispecifics, proteins, conjugates, etc.) and genetic medicines (AAV, LNPs, siRNA etc.) for all therapeutic areas across discovery.
Job Description 
The Principal Data Architect is a visionary leader in the development and success of our cloud-native data platform, which supports the development and integration of predictive and generative machine learning solutions in drug discovery scientist workflows. This role requires a strong ability to see both the big picture and the details, and to work cross-functionally with both wet lab scientists, ML engineers, software engineers, data engineers, and data infrastructure engineers, among others.
This position reports to the Head of AI/ML in Biotherapeutics and Genetic Medicine (BGM) and will serve as a trusted advisor to senior leadership. This role is pivotal in driving our organization towards becoming a leader in the application of artificial intelligence, ensuring that AI and ML initiatives are built on a robust, resilient, and scalable data foundation that grows with the organization.
Key responsibilities:
<ul>
<li>Drive the vision, execution, implementation, adoption, and continuous improvement of a robust, scalable data platform as the foundation for the execution of AbbVie’s AI/ML strategy, particularly within BGM.&nbsp;</li>
<li>Define data models and architectures that collect, store, structure, access, and connect datasets generated across a dozen different lab groups, enabling downstream uses (ML model development, operational reports, lab documentation, etc.).&nbsp;</li>
<li>Collaborate closely with wet lab scientists, especially the Head of Lab Data Products, and automation engineers to maximize the utility of data captured by lab automation workflows.&nbsp;</li>
<li>Collaborate closely with data scientists, and deployment engineers, to ensure data pipelines support both machine learning model development and deployment into production. &nbsp;</li>
<li>Co-develop and execute a strategy that maximizes FAIR-fication of BGM data and in concert with wider BGM strategic goals.&nbsp;&nbsp;</li>
<li>Communicate the impact of a robust data platform to AbbVie’s drug pipeline, using both user stories and KPIs that allow measurement of the value added.&nbsp;</li>
<li>Multiply impact of the data platform by championing and communicating the principles behind connected data, data stewardship, data-as-a-product, and cloud-first and cloud-native architectures.&nbsp;</li>
<li>Collaborate with data infrastructure and data governance experts across AbbVie to ensure that data governance principles and policy are optimally implemented.&nbsp;&nbsp;</li>
<li>Ensure alignment and coordination of data infrastructure initiatives with existing AbbVie initiatives such as Convergence, and ARCH.</li>
</ul>
Qualifications 
<ul>
<li>BS, MS, or PhD in&nbsp;computer science, data science, computational biology, computational chemistry, computational biophysics, or related field with typically 16+ (BS) years, 14+ (MS) years, or 8+ (PhD) years of &nbsp;experience in data architecture&nbsp;with a track record of designing enterprise data platforms.&nbsp;&nbsp;</li>
<li>Deep technical skills in data modeling, data integration, implementation of data storage solutions, data pipelines, and integration with AI/ML.&nbsp;&nbsp;</li>
<li>Production programming expertise in SQL, python, or Java.&nbsp;</li>
<li>Experience building cloud data infrastructure solutions using AWS, Azure, or GCP.&nbsp;</li>
<li>Familiar with both wet and dry lab scientific principles and processes, able to foresee and prevent data platform-originating failure modes.&nbsp;</li>
<li>Experience with cross-functional team leadership, and track record of collaboration excellence.&nbsp;</li>
<li>Previous experience in the pharmaceutical or biotechnology sectors.&nbsp;&nbsp;</li>
<li>Experience managing both team member delivery and career development.&nbsp;</li>
<li>Exceptional interpersonal and communication skills, and strong evidence of ability to build stakeholder alignment.&nbsp;&nbsp;</li>
<li>Ability to integrate data governance principles into everyday decision making.&nbsp;</li>
</ul>
The position is located at Worcester, MA site as a full time in office or hybrid (3 days per week) role.&nbsp;
 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 thetime&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.&nbsp;​
</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 anybonus,&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 soleand&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>

Principal Research Scientist II- Data Architecture, Biotherapeutics and Genetic Medicine

<h3>Job Description</h3>
Research Analyst I - Separation-based assays
Location: Worcester, MA (100 Research Drive)
Hours: The schedule will be 9am-5pm Mon-Fri onsite.
1 year contract
Hourly Pay Rate: $31-34/hr (individual medical benefits available at a cost)
We are seeking a dedicated Research Analyst I specializing in separation-based assays to join our innovative research team. This role involves designing, executing, and analyzing experiments focused on separation techniques used in biological and chemical research. The ideal candidate will contribute to advancing our understanding of complex biological systems through precise assay development and data interpretation. This position offers an exciting opportunity to work at the forefront of scientific discovery, supporting projects that have significant implications for health, technology, and fundamental science.
 
 The Research Analyst independently generates precise, reliable and reproducible data in a timely manner. Demonstrate experimental precision and strong data interpretation skills and should possess understanding of core discipline.
 
Responsibilities:
<ul>
<li>Perform routine tasks independently and generate reliable and consistent results.</li>
<li>Analyze and critique results, noting significant deviations.</li>
<li>Troubleshoot experiments and instrumentation.</li>
<li>Learn and understand new experimental techniques.</li>
<li>Demonstrate skill in multiple techniques and appropriately modify protocols, as required, to suit the changing needs of research programs.</li>
<li>Present interpreted results and updates internally in a timely and professional manner</li>
<li>Place data in proper scientific context by consulting and citing relevant literature.</li>
<li>Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, and GxP compliance.</li>
</ul>
 
Qualifications:
<ul>
<li>Bachelor’s or Master’s Degree in Biochemistry/Biophysics, Chemistry, or equivalent, with typically 3 years’ experience</li>
<li>Theoretical and practical knowledge to carry out method development and qualification.</li>
<li>Experience in separation-based assays including but not limited to UPLC/HPLC based methods, capillary electrophoresis (CE), and imaged capillary isoelectric focusing (icIEF)</li>
</ul>
 
Our role in supporting diversity and inclusion
 As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.

Research Analyst I - Separation-based assays

<h3>Job Description</h3>
Job Description
Background: Tri-K is one of leading suppliers of natural actives such as proteins, peptides and a comprehensive cosmetic ingredients portfolio to the personal care industry. It has an R&amp;D center with state-of-the-art equipment and testing facilities. To strengthen its innovation capabilities and improve customer connectivity, the R&amp;D organization focuses on developing new innovative ideas, products, and formulations with proven efficacy. This senior level R&amp;D position is part of the manufacturing organization based in Derry, NH

Summary: 
We are seeking a highly motivated and experienced protein chemist to join our team. The ideal candidate should have a PhD in protein chemistry, biochemistry, or a related field, or have at least 3 years of experience in protein synthesis, characterization, purification, and analysis.
Essential Duties and Responsibilities include the following. Other duties may be assigned. 
<ul>
<li>Develop and optimize protein and peptide purification protocols.</li>
<li>Characterize and analyze proteins and peptides using techniques such as HPLC, SDS-PAGE, and LC-MS</li>
<li>Perform chemical reactions to implement protein modification. </li>
<li>Conduct protein stability studies and develop formulations to improve protein stability.</li>
<li>Collaborate with other scientists to develop new protein-based cosmetic ingredients and products.</li>
<li>Maintain and troubleshoot laboratory equipment.</li>
<li>Write technical reports and present findings to internal and external stakeholders.</li>
</ul>
<ul>
<li>Search and evaluate published literature to understand hair and skin substrates, new protein technologies and new methodologies.</li>
</ul>
<ul>
<li>Research the latest market trends, customer needs, and competitor positioning.</li>
<li>Provide guidance to the Technical Services Team in addressing customer inquiries in a direct and succinct manner.</li>
<li>Collaborate with the Sales, Marketing and Business Managers, to ensure effective marketing claims, and to ensure continued positive client relationships and to build relationships with new clients.</li>
</ul>
<ul>
<li>Investigate possibilities and benefits of line extensions and functional blends surpassing industry standards. </li>
<li>Research the feasibility of combining proteins with other chemistries and technology promoting synergistic effects.</li>
<li>Research prior patents to allow for “freedom to operate”. </li>
</ul>
<ul>
<li>Explore new partnerships and collaborations with academia. </li>
</ul>
Required Skills and Competencies
Strong Technical Background in Protein/Peptide Chemistry is required. The incumbent must have a strong understanding of protein/peptide behavior to modify, identify and purify the active proteins/peptides from a complex natural source. He/She should be open to new challenges and be able to implement creative and innovative approaches. 
Competencies
To perform the job successfully, an individual should demonstrate the following competencies:
<ul>
<li>Strong knowledge of protein chemistry and biochemistry</li>
<li>Experience with protein purification techniques such as chromatography and ultrafiltration</li>
<li>Experience with protein analysis techniques such as HPLC, SDS-PAGE, and LC-MS</li>
<li>Strong problem-solving and analytical skills</li>
<li>Excellent communication and interpersonal skills</li>
<li>Ability to work independently and in a team environment.</li>
<li>Strong technical, and strategic acumen. </li>
<li>Exceptional verbal, written communication, and presentation skills</li>
<li>Comfort &amp; capability to work effectively in a collaborative cross-functional organization.</li>
<li>Analytical, and Problem-Solving skills to find effective solutions and overcome challenges. </li>
<li>Project Management - Develop project plans; Complete projects on time and budget. </li>
<li>Strong time management and prioritization skills. </li>
<li>Innovation - Develop and present innovative approaches and ideas. </li>
</ul>

Qualifications:
The requirements listed below are representative of the knowledge, skill, and/or ability required.
Education/Experience:
PhD in protein chemistry, biochemistry, or a related field. Or have at least 3 years of experience in protein synthesis, characterization, purification, and analysis.
Scientific Language Ability:
Ability to read, analyze, and interpret scientific periodicals, professional journals, technical procedures, or governmental regulations. Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, and customers.
Analytical skills: 
Ability to solve practical problems and deal with numerous assumptions and variables in situations where only limited standardization exists. Knowledge of MS Suite and other PC tools is essential.
Physical Demands:
This position requires working at the Derry, NH R&amp;D center 5 days a week, unless travelling to attend trade shows or visit other Tri-K sites. 
Travel Requirements:
10% travel including domestic/international with overnight stays to drive business development efforts.

Senior Protein Chemist

<h3>Job Description</h3>
Job Description
Job Title: Senior Scientist
Job Description
We are seeking a highly skilled and motivated Senior Scientist to join our team. This role involves the start-up of a lab, including the setup of single-use technology bioreactors, ensuring all documentation meets compliance and validation standards. The successful candidate will manage materials and inventory, establish a structured storage area, and implement an efficient inventory management system. Additionally, you will support project and operational activities, assisting the project team in achieving daily and weekly milestones and facilitating lab equipment testing and setup.
Responsibilities
<ul>
<li>Setup single-use technology bioreactors, including equipment delivery, unboxing, assembly, setup, and operation.</li>
<li>Troubleshoot issues and ensure documentation meets compliance and validation standards.</li>
<li>Establish and organize a structured storage area for raw materials and spare equipment.</li>
<li>Implement an inventory management system to track consumables, reagents, and spare parts.</li>
<li>Support the overall project team in meeting key daily and weekly milestones.</li>
<li>Facilitate receipt, setup, and functional testing of lab equipment at all scales.</li>
<li>Develop and maintain a list of spares for all deployed equipment.</li>
</ul>
Essential Skills
<ul>
<li>Experienced with single-use technology bioreactors: unbox, setup, start-up, troubleshoot, and operate.</li>
<li>Understanding of turnover packages (TOPs).</li>
<li>Proficiency with DeltaV distributed control system.</li>
<li>Bachelor’s degree in Biotechnology, Biochemistry, Chemical Engineering, or a related field.</li>
<li>Minimum 5 years of experience in lab operations or bioprocessing involving single-use technologies.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Proven ability to work cross-functionally with engineering, procurement, and project management teams.</li>
<li>Comfortable working with a remote manager and providing weekly updates.</li>
<li>Willingness to track work completed on a weekly basis and monitor deliverables.</li>
<li>Ability to organize schedule and work independently.</li>
</ul>
Work Environment
This role is based in a lab environment onsite, requiring hands-on work with advanced technologies and equipment. The successful candidate will be comfortable working independently and collaboratively, with a focus on achieving project milestones and maintaining an organized workspace.
Job Type &amp; Location
This is a Contract position based out of Plainville, MA.
Pay and Benefits
The pay range for this position is $57.00 - $70.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Plainville,MA.
Application Deadline
This position is anticipated to close on Dec 15, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Senior Scientist

<h3>Job Description</h3>
Job Description
Part Time Shift: Weekends, rotating Hourly Pay Range: $25.00-$30.00 (Based on experience)
POSITION SUMMARY 
Performs lab testing and associated activities within the Microbiology section, including Serology, Virology and Parasitology.
Essential Position Duties 
<ul>
<li>Reviews the daily specimen management report.</li>
<li>Troubleshoots and maintains the LIS and instruments interface and software.</li>
<li>Performs Clostidium difficile assays.</li>
<li>Resolves client problems as needed.</li>
<li>Performs and records all quality assurances systems required to maintain precision and accuracy, including proficiency testing.</li>
<li>Performs other tasks and procedures in Microbiology as required which are commensurate with education, training and experience.</li>
<li>Assists in maintaining adequate inventory of supplies.</li>
<li>Record lot numbers and ensures compliance with State requirements for documentation of lot numbers with quality control and specimen records.</li>
<li>Performs all clerical functions associated with the department.</li>
<li>Reads bacterial and viral cultures. Performs biochemical identification procedures as necessary and record MIC results. </li>
<li>Follows all safety protocols as outlines in safety manual.</li>
<li>Identifies and pursues self improvement needs.</li>
<li>Seeks coaching/mentoring when appropriate.</li>
<li>Performs other duties as assigned</li>
</ul>
Compliance Responsibilities 
<ul>
<li>Participates in required orientation, Compliance and HIPAA training programs.</li>
<li>Cooperates with monitoring and audit functions and investigations.</li>
<li>Participates, as requested, in process improvement responsibilities.</li>
</ul>
POSITION QUALIFICATIONS 
Core Competencies/Skill Sets 
<ul>
<li>Excellent verbal and written communication skills.</li>
<li>Detail oriented and organizational skills.</li>
<li>Exercises accuracy and precision in completion of prescribed tasks and treatments.</li>
</ul>
Professional Experience/Educational Requirements 
<ul>
<li>Bachelor’s degree or MT (ASCP or equivalent preferred); Associates degree with MLT</li>
<li>Minimum of one (1) year experience in the area of Microbiology.</li>
<li>Some computer experience required.</li>
</ul>
Certification/Licensure
<ul>
<li>Must qualify as a clinical laboratory technologist under CLIA regulations.</li>
</ul>
Benefits:
TridentCare offers a competitive wage and robust benefit package to full time employees. Part time employees are eligible for many of the same below, pro-rated. Benefits include:
<ul>
<li>Two weeks of vacation time</li>
<li>Health Insurance after 30 days!</li>
<li>Sick time</li>
<li>8 paid holidays</li>
<li>Same day pay available</li>
<li>Medical insurance allowance, giving you the freedom to customize your plan to fit your needs</li>
<li>Dental insurance</li>
<li>Vision insurance</li>
<li>Disability insurance</li>
<li>Company paid life insurance</li>
<li>401(k)</li>
</ul>
#MBX

Microbiologist/ MLT, Microbiologist

<h3>Job Description</h3>
Job Description
Discover Veranova:
At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented 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 Process R&amp;D Scientist plays a key role in developing and optimizing synthetic routes for complex active pharmaceutical ingredients (APIs). This position conducts small- to large-scale chemical reactions and generates high-quality data that supports project decision-making and innovation. Working under the guidance of technical leads, the role contributes to delivering projects on time, on spec, and within budget. It’s an excellent opportunity to deepen expertise while supporting impactful pharmaceutical development.
Core Responsibilities: 
<ul>
<li>Delivers experimental output with high scientific integrity, meeting targets, timelines, and quality expectations with guidance.</li>
<li>Exhibits strong safety awareness, conducts laboratory and operational activities safely, and maintains accountability for safe behavior in the work environment.</li>
<li>Maintains technical equipment and related services to ensure proper functionality.</li>
<li>Acts on feedback and demonstrates a continuous commitment to learning and professional development.</li>
<li>Leads technical and operational areas and supports troubleshooting for complex scientific issues with minimal guidance.</li>
<li>Shares knowledge, skills, and experience effectively with internal and external stakeholders; may lead focused projects as a key contact.</li>
<li>Keeps accurate, legible, and complete records of all experiments, observations, and equipment use.</li>
<li>Writes high-quality reports and delivers presentations to customers and management with some guidance, aligned with project milestones.</li>
<li>Contributes to maintaining strong customer relationships and identifies new commercial opportunities.</li>
<li>Actively supports the technical development of the department and the broader organization.</li>
<li>Ensures all documentation meets Veranova standards; supports audit readiness and participates in regulatory and customer audits as needed; reports near misses and safety incidents per company procedures; and ensures all work complies with applicable state and federal regulations, including GMP, DEA, and FDA requirements.</li>
<li>Adheres to all EHS policies and procedures; demonstrates strong technical and procedural proficiency in applying EHS standards; supports EHS audit readiness and participates in audits; reports and cooperates fully in investigations of near misses and incidents; and upholds Veranova’s EHS commitments by integrating ISO 14001, OHSAS 18001, and Sustainability 2025 principles into daily work.</li>
<li>Performs additional duties within the employee’s skills and abilities as reasonably assigned.</li>
</ul>
Qualifications: 
Required
<ul>
<li>PhD degree (or equivalent experience) in a chemistry related discipline.</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>
Special Factors 
<ul>
<li>Must be able to stand, walk, and manually operate objects, tools, or controls; reach with hands or arms; and climb, balance, stoop, kneel, or crouch when necessary for the job activity.</li>
<li>Must be able to 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>May regularly work with moving mechanical parts and may work with toxic or caustic chemicals.</li>
<li>May work in humid areas with low or high temperatures.</li>
<li>May be required to work with a respirator or operate with full-body Tyvek suits and supplied air or PAPR.</li>
</ul>
Salary Range: $105,000 - $120,000 annual base salary 
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: Veranova is committed to fair and transparent compensation practices. This includes a competitive base salary, eligibility for performance-based bonuses, and an attractive 401(k) Plan with company match. Salary ranges reflect the scope and expectations of the role, and are based on market data, internal equity, and role-specific factors. Final compensation may vary depending on experience, skills, education, and business needs.</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 welcome people with diverse experiences and perspectives who share our mission to improve and save lives. Even if you don’t meet every qualification, we encourage you to apply. Veterans, first responders, and those transitioning from military to civilian life bring valuable skills that strengthen our team.</li>
</ul>
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. 
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.
#LI-Onsite

Scientist - Process Research & Development

<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
If you’re looking for a rewarding career, a place to call home, apply with us today.
Job Description 
We are seeking a highly skilled, passionate, and motivated scientist to join our diabetes team. This position will play a key lab-based role in advancing iPSC stem cell engineering and will contribute to the development of the next generation of islet cell therapies. Successful candidates will have experience with gene editing, molecular biology techniques, assay development, and human iPSC cell culture, differentiation, and banking.
Key Responsibilities:
<ul>
<li>Enabling and advancing iPSC gene editing, cell line development, and evaluation of differentiated cells.</li>
<li>Routine iPSC cell culture, passaging, and media making.</li>
<li>Optimize workflows for iPSC CRISPR based gene-editing, gRNA screening, and delivery.</li>
<li>Optimize and perform assays for on-/off-target analysis via PCR and NGS workflows.</li>
<li>Generate clonal gene edited iPSC lines and characterize via flow cytometry, ddPCR, dPCR and qPCR.</li>
<li>Culture and execute routine directed differentiation of human iPSCs to pancreatic islets performing drug substance assessments such as cell counts, viability, and metabolite assessments.</li>
<li>Assist scientists in the team to evaluate and design mitigation strategies to ensure genomic stability of the iPSC lines and drug substance.</li>
<li>Collaborate cross-functionally to support transfer of R&amp;D assays to GMP.</li>
<li>Maintain accurate and detailed records of all experiments, synthesize results, prepare reports, and present in meetings. Contribute to SOP development.</li>
<li>Work seamlessly in executing workplans and meeting deadlines.</li>
</ul>
Qualifications 
Minimum Required Qualifications:
<ul>
<li>B.S. in Stem Cell Biology, Cell Biology, Bioengineering or a related field with 3-4 years relevant industry experience in gene editing and cell therapy.&nbsp; M.S. in Stem Cell Biology, Cell Biology, Bioengineering or related field with 1-2 years relevant industry experience in gene editing and cell therapy.</li>
<li>Extensive hands-on experience with human iPSC culture, gene editing, and molecular biology techniques.</li>
<li>Proficiency in CRISPR gene editing and cell line development, including optimization of protocols, familiarity with flow-based sorting.</li>
<li>Proficiency in molecular biology techniques including construct design, PCR, ddPCR, dPCR, and NGS.</li>
<li>Hands-on experience with assay development including luciferase assays, ELISA, and flow cytometry.</li>
<li>Hands-on experience with cell delivery methods of gene editing tools.</li>
<li>Excellent communication and interpersonal skills, with the ability to work effectively in a team-oriented environment.</li>
<li>Strong organizational skills and diligent record keeping.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Hands-on experience in pancreatic islet directed differentiation.</li>
<li>Hands-on experience in transitioning research-grade processes to GMP-grade.</li>
<li>Familiarity with electronic lab notebook (ELN) documentation.</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship.</li>
</ul>
 Additional Information 
Position is Full Time, Monday-Friday, 8am-5pm with occasional weekends (on a rotational basis to support cell culture). Candidates currently living within a commutable distance of Boston, MA are encouraged to apply.
What to Expect in the Hiring Process: 
<ul>
<li>10-15 Minute Phone Interview with Region Recruiter</li>
<li>45-60 Minute Virtual Interview with Manager and/or Group Leader</li>
<li>45-60 Minute In-Person Meeting over Coffee for a Casual Discussion of the Role</li>
</ul>
What We Offer:
<ul>
<li>Target pay range: $37-41/hr</li>
<li>Excellent full-time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>Yearly goal-based bonus &amp; eligibility for merit-based increases</li>
</ul>
Eurofins Lancaster Laboratories Professional Scientific Services® (PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website <a href="http://www.eurofinsus.com" target="_blank">www.eurofinsus.com</a>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

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