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<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:
Under the direction of a Production Supervisor and Production Shift Lead chemist, the Kilo Chemist works on manufacturing Active Pharmaceutical Ingredients (APIs) in support of the business unit while meeting local, state, and federal quality and safety regulations.
Core Responsibilities: 
<ul>
<li>Independently synthesize, purify, and isolate chemical intermediates and active ingredients. </li>
<li>Communicate with Shift Leader regarding safety, production, quality, or any other operational issues on shift.</li>
<li>Actively participates in pre-shift meetings to develop individual work plans.</li>
<li>Completely and accurately record data such as temperature of equipment, hours of operations, raw materials, and pressure of large-scale reactors in accordance with good documentation practices.</li>
<li>Exhibit an elevated level of safety awareness and conduct lab operations in a safe manner.</li>
<li>Maintain a clean kilo lab and ensure equipment is cleaned after use. Ensure support and work areas meet all requirements for housekeeping. </li>
</ul>
Qualifications: 

Required
<ul>
<li>Bachelor’s degree in chemistry or a minimum of 3-5 years' experience as a chemical operator</li>
<li>Must be open to rotating 1st, 2nd, and 3rd shifts</li>
<li>Elevated level of safety awareness and attention to detail </li>
<li>Must have the ability to read and interpret complex operating instructions</li>
<li>Excellent organizational and record keeping skills </li>
<li>While performing the duties of this job it is required to stand, walk, and use hands to operate objects, tools, or controls; reach with hands or arms; climb, balance, stoop, kneel, or crouch when necessary for job activity.</li>
<li>Must be able to lift and/or move up to 50 pounds.</li>
<li>Perform other job-related duties as assigned.</li>
</ul>
Preferred

<ul>
<li>Prior basic laboratory skills and a working theoretical knowledge of organic chemistry</li>
<li>Experience working in a Kilo-Lab environment or GMP experience </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>
</ul>
<ul>
<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>
</ul>
<ul>
<li>Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.</li>
</ul>
<ul>
<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 misson 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.

Kilo Chemist

<h3>Job Description</h3>
Job Description
Team up with the most innovative company where Imagination becomes reality! E Ink is the originator, pioneer, and commercial leader in ePaper technology. The Billerica Research &amp; Development team is thriving and growing as we help develop products that are changing how people access information every day. We are seeking qualified candidates who are self-driven, looking to advance their career and become a high-impact player on a team.
Based on technology from MIT’s Media Lab, E Ink has transformed and defined the eReader market. Its Electrophoretic Display products make it the worldwide leader for ePaper. The Company’s corporate philosophy aims to deliver revolutionary products, user experiences and environmental benefits through advanced technology development.
Our diversity of people, backgrounds, experiences, thoughts and perspectives is fostered to create an inclusive work environment.
Our culture is built on value commitments to innovation, quality, results, integrity, community, people, and collaboration that foster a strong employee engagement, teamwork, safety and wellness.
We offer a competitive/generous benefits package that fits the needs of our employees. It includes health, dental, vision, wellness programs, employee discounts, 401k matches, ongoing development, advancement opportunities and more. This position is also eligible for our bonus program. (see E Ink │ Our Company)
About the position:
E Ink is seeking an innovative and results-focused Materials Scientist to help engineer materials for better performance, reliability and consistency via modern inverse design techniques. In this role, you will be working with wet / dry lab practices and techniques to determine rapid screening pipelines that enable collection of large datasets related to E Ink-specific material sets. As the glue between collaborators working with materials and AI-focused scientists, you will be expected to connect the worlds to enable accurate, high-throughput models that can be used to accelerate inverse design of materials. As part of our innovative team, you will be instrumental in enabling these pipelines to operate at scale, with the goal of &gt;100x in the throughput over the next year. In this role, you will work in a collaborative development team environment and work closely with other research teams. As a member of this new initiative, you will be expected to take a leadership role in spearheading this new initiative and delivering results. The successful candidate will have strong analytical and communication skills, and a record of driving toward pragmatic solutions to industrial problems.
Responsibilities:
<ul>
<li>Design and maintain reproducible pipelines (software / hardware) that generate experimental data, engineer materials-centric features, and train predictive or generative ML models</li>
<li>Conduct inverse-design campaigns (Bayesian optimization, diffusion models, genetic algorithms, etc.) to recommend new formulations, coordinate lab validation and iterate</li>
<li>Dive deep into fundamental ink dynamics and chemistries to discover key insights related to material properties and chemical design</li>
<li>Invent and document relevant intellectual property and present findings to broad audiences</li>
<li>Champion best practices in data quality and experiment lineage across the organization</li>
<li>Act as the glue between collaborators working at the interface of soft-matter science and machine learning</li>
</ul>
Ideal Qualifications:
<ul>
<li>Minimum of a Ph.D. (or exceptional M.S. plus 4 years' experience) in Materials Science, Chemistry, Chemical Engineering, Physics, Applied Math, or similar major. Outstanding candidates of any educational background will be considered</li>
<li>Background in physical chemistry, electrochemistry or colloids</li>
<li>Experience with soft-matter, colloidal, electrochemistry and / or polymer systems</li>
<li>Experience with modern materials discovery workflows</li>
<li>Proficiency in Python or other scientific programming tools</li>
<li>Strong problem-solving skills and the ability to work collaboratively in a multidisciplinary team</li>
<li>Ability and openness to learn new tools and techniques and share examples</li>
<li>Excellent communication skills and a collaborative mindset</li>
</ul>
Benefits:
<ul>
<li>Competitive total compensation package</li>
<li>Medical, dental and vision on 1st day</li>
<li>Company 401K match</li>
<li>20 PTO days</li>
<li>Generous sick leave policy</li>
<li>Casual day to day work environment</li>
<li>Hybrid/flexible work environment (for some positions)</li>
</ul>
E ink is committed to a diverse and inclusive workforce. E Ink is an equal opportunity employer and does not discriminate on the basis of race, ethnicity, gender, identity, sexual orientation, veteran’s status, disability, age, or on any basis prohibited by federal and state law.

AI / Materials Research Scientist 1900S-2

<h3>Job Description</h3>
Job DescriptionJob Title: Sr ScientistJob Description
Join our team as a Sr Scientist, where you will support the Analytical Method Development Team as a Subject Matter Expert. You will be instrumental in test method transfer, analytical test method validation, and driving continuous improvement initiatives. Your expertise will also contribute to test method validation, process validation, and QC testing and development on lipid nanoparticles (LNPs). Additionally, you will support deviations and investigations for Out of Specification (OOS) results, Corrective and Preventive Actions (CAPA), and root cause analysis.
Responsibilities
<ul>
<li>Serve as a Subject Matter Expert for test method transfer and analytical test method validation.</li>
<li>Assist with test method validation and process validation.</li>
<li>Support QC testing and development on lipid nanoparticles (LNPs).</li>
<li>Investigate deviations and support OOS, CAPA, and root cause analysis.</li>
<li>Drive continuous improvements in processes and methodologies.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in method development, analytical chemistry, and quality control.</li>
<li>Experience with HPLC, validation, LNP, and protein assays.</li>
<li>Strong knowledge of analytical method development, protein chemistry, ELISA, capillary electrophoresis, FDA regulations, and PCR.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Bachelor's degree with 10+ years of experience, Master's degree with 7+ years of experience, or PhD with 5+ years of experience.</li>
<li>Understanding of HPLC, capillary electrophoresis, and PCR.</li>
<li>Experience mentoring and supporting the development of junior scientists.</li>
</ul>
Work Environment
This role is 100% onsite, operating Monday to Friday from 9:00 am to 5:00 pm. The position requires travel to Fargo, North Dakota. You will be an individual contributor with responsibilities to mentor other scientists, working within a team of nine and reporting directly to the Sr Manager of Method Validation. High degrees of collaboration and communication skills are essential in this dynamic and growth-oriented environment.
Pay and Benefits
The pay range for this position is $100000.00 - $110000.00/yr.
They will receive health, dental, vision, 401k. They will get holidays and vacation time as well and a yearly bonus of 10%.
Workplace Type
This is a fully onsite position in Waltham,MA.
Application Deadline
This position is anticipated to close on Jul 28, 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
For more than 50 years, EdgeTech has been the industry leader in the design and manufacture of advanced underwater sonar systems for applications involving seabed survey, target detection, object identification, mooring instrumentation, and acoustic tracking/positioning.&nbsp; Our products are used to support a variety of customers, from offshore oil and gas to fisheries/science/underwater research, defense, and police/fire search and rescue
We’re looking for an engineer/scientist with interest in applying signal processing to develop algorithms that enable new capabilities in next-generation sonar systems. Typical assignments include algorithm design, analysis, and implementation; sonar system analysis; involvement in software and hardware prototyping and test activities; documentation and planning; as well as sea testing, data collection, and post-trial analysis.
Job Responsibilities
<ul>
<li>Design algorithms for processing of sonar signals including waveform design, beamforming, broadband processing, and detection.</li>
<li>Develop processing algorithms and assess their performance. Interpret results.</li>
<li>Collaborate with real-time code developers and modeling/simulation analysts to develop and integrate system software.</li>
<li>Develop simple and reliable signal processing algorithms for a variety of processors, to include ARM’s, SoC’s/SoM's and FPGAs</li>
<li>Assist with the development of signal processing specifications and their implementation</li>
<li>Test software, firmware and full sonar solutions in simulation, hardware-in-the-loop, and field demonstrations</li>
<li>Collaborate with a cross-functional team testing your contributions and analyzing performance</li>
<li>Support the engineering, production, and sales/marketing teams with productization of technologies and solutions</li>
<li>Understand broad product objectives to develop and maintain relationships with major customers.</li>
<li>Collaborate with other engineers, customers and the technical community to advance sonar capabilities for current and future applications</li>
</ul>
Job Requirements
<ul>
<li>This job can be filled at multiple levels, depending upon the successful candidate’s education and experience. Minimum education required is an M.S. degree in an engineering or science related discipline plus five year’s related experience or an equivalent combination of education and experience.</li>
<li>Experience with signal processing theory and applications</li>
<li>Experience with scripting and analysis tools such as Matlab and Python</li>
<li>Experience with planning and conducting sea trials and surveys.</li>
<li>Highly effective written and verbal communication skills</li>
<li>Ability to work effectively in a team and set priorities</li>
<li>Work with sonar imaging technologies or hydrographic applications is a big plus.</li>
<li>Familiarity with hardware (amplifiers, antennas/transducers, filters), and digital processing with FPGAs, GPUs, CPUs, is desirable but not required.</li>
<li>Work will include a mix of field and office assignments, with domestic and international travel as part of the job.</li>
</ul>
If interested, please contact:
Kevin Igo
<a href="mailto:Kevin.Igo@edgetech.com" target="_blank">Kevin.Igo@edgetech.com</a>
Company DescriptionEdgeTech is a leading manufacturer of underwater technology solutions. The company is known worldwide for its high quality products which include: side scan sonars, sub-bottom profilers, bathymetry systems, AUV and ROV-based sonar systems, combined and customized solutions. In addition to the full line of underwater survey products, EdgeTech provides reliable USBL systems, transponder beacons, deep sea acoustic releases, shallow water and long life acoustic releases, MRUs and customized underwater acoustic command and control systems. 
<h3>Company Description</h3>
EdgeTech is a leading manufacturer of underwater technology solutions. The company is known worldwide for its high quality products which include: side scan sonars, sub-bottom profilers, bathymetry systems, AUV and ROV-based sonar systems, combined and customized solutions. In addition to the full line of underwater survey products, EdgeTech provides reliable USBL systems, transponder beacons, deep sea acoustic releases, shallow water and long life acoustic releases, MRUs and customized underwater acoustic command and control systems.

Applied Research Scientist

<h3>Job Description</h3>
Job Description
Quality Metrology Technician
The Quality Metrology Technician is responsible for supporting quality assurance and metrology functions to ensure that products meet internal and customer specifications. This role involves analyzing processes, identifying root causes of defects, recommending improvements, and supporting validation and inspection activities. The technician works closely with engineering, production, and quality teams to drive continuous improvement and maintain compliance with regulatory standards. &nbsp;
KEY ACCOUNTABILITIES:
Quality Assurance &amp; Compliance
<ul>
<li>Adhere to all company policies and serve as a role model in policy interpretation and customer service.</li>
<li>Provide training support for:</li>
<li>ISO 13485 requirements</li>
<li>FDA CFR 820 regulations</li>
<li>Micron Quality System requirements</li>
<li>Auditing and Statistical Process Control (SPC)</li>
</ul>
Metrology &amp; Inspection
<ul>
<li>Program, set up and operate inspection/metrology equipment, including CMMs and optical/mechanical tools.</li>
<li>Establish measurement methodologies for plastics or metals substrate.</li>
<li>Schedule and manage measurement activities (i.e Gage R&amp;R and Bias studies)</li>
</ul>
Cross Functional Collaboration
<ul>
<li>Support manufacturing, product development, and project teams with metrology input and recommendations.</li>
<li>Work with internal and external customers to verify product specifications and define acceptable variate levels.</li>
</ul>
Document &amp; Process Control
<ul>
<li>Develop and analyze production and statistical data to ensure processes meet quality expectations and identify improvement opportunities.&nbsp;</li>
<li>Ability to work within a statistical sampling plan (i.e. ANSIZ1.4)</li>
</ul>
Validation
<ul>
<li>Assist in developing measurement qualifications to be used with validation plans for products</li>
</ul>
JOB QUALIFICATIONS: Education &amp; Experience
<ul>
<li>Bachelor’s degree in engineering or related field, or a minimum of 5 years in a Metrologist role</li>
<li>Medical device manufacturing experience preferred</li>
<li>ASQ Certified Calibration Technician (Preferred)</li>
</ul>
Technical Skills
<ul>
<li>Strong understanding of metrology and statistical analysis.</li>
<li>Working knowledge of plastics injection molding and metal manufacturing</li>
<li>Proficient in CMM operation and programming (minimum 3-5 years with Hexagon PC-DMIS).</li>
<li>Skilled in using optical and mechanical measurement tools.</li>
<li>Experience with ERP systems (IQMS preferred).</li>
<li>Familiarity with ISO 13485 and FDA CFR 820 regulations.</li>
<li>Proficient in Microsoft Office Suite and Mini Tab</li>
</ul>
Company DescriptionConnexion Systems &amp; Engineering is a full-service staffing firm, whose mission is to provide "best in class" staffing services to our clients and job seekers alike. We strive to achieve excellence in staffing, job placement and recruiting services, while treating our clients, employees, and candidates with the professionalism and respect they deserve. 
<h3>Company Description</h3>
Connexion Systems &amp; Engineering is a full-service staffing firm, whose mission is to provide "best in class" staffing services to our clients and job seekers alike. We strive to achieve excellence in staffing, job placement and recruiting services, while treating our clients, employees, and candidates with the professionalism and respect they deserve.

Quality Metrology Technician

<h3>Job Description</h3>
Job Description
JOB SUMMARY
The Cultivation Technician will perform manual labor to assist in the upkeep, stocking, and fulfillment of growing cannabis, including, but not limited to; watering, feeding, pruning, cloning, cleaning, and transplanting. This position will report to the Cultivation Manager. 
PRIMARY RESPONSIBILITES 
<ul>
<li>Daily care of cannabis plants, including watering, pruning and trimming, inspecting the plants. </li>
<li>Fertilizing and providing nutrients to the plants according to cultivation protocols</li>
<li>Careful monitoring of the plants for any signs of growing issues or problems; treatment for disease or infestation.</li>
<li>Ensure the appropriate information is accurate and listed clearly in accordance with the state regulations and company standard operating procedures.</li>
<li>Carefully follow directions as provided by the Cultivation Department</li>
<li>Willingness to continue to learn best practices of cannabis cultivation with a strong interest in horticulture, agriculture and greenhouse operating systems.</li>
<li>Sweeping, mopping and all other required cleaning</li>
<li>Cleaning of the plant housing devices</li>
<li>Maintenance and cleaning of the plant tables</li>
<li>Maintenance of the plant pots</li>
<li>Reporting any issues to management to ensure a timely fix</li>
</ul>
JOB REQUIREMENTS 
<ul>
<li>Must be 21 years or older</li>
<li>Well organized and ability to keep deadlines</li>
<li>Ability to work in a team environment to achieve company goals</li>
<li>Effective time-management skills and ability to multi-task</li>
<li>Ability to work in a fast-paced, changing, and challenging environment</li>
<li>The willingness to continue to learn and grow with the company, improve cultivation skills and gain greater knowledge of cultivation processes.</li>
<li>Basic Excel, Word, and general computer knowledge</li>
<li>Full knowledge of all applicable law, regulations, and requirements; maintaining facility at 100% compliance at all times; this includes being up to date on any changes to current applicable laws/regulations </li>
<li>Must be and remain compliant with all regulatory requirements for working in the cannabis industry</li>
<li>Must be able to obtain and retain a Registered Agent Card issued by the state of operation</li>
<li>Must be focused, pay close attention to detail</li>
<li>Must be able to internalize training and follow instructions </li>
<li>Must be able to communicate clearly and effectively</li>
<li>Other duties and responsibilities</li>
</ul>
COMPANY OVERVIEW
Ascend Wellness Holdings (AWH) is a vertically integrated cannabis cultivator, processor and provisioning center operator with assets in Illinois, Maryland, Massachusetts, Michigan, New Jersey, Ohio and Pennsylvania. We seek to foster a robust and inclusive cannabis industry through a premium, unmatched customer-focused retail experience. We are looking to build a world-class team that will help carry out our mission of helping to shape the future of cannabis as a leading healthcare solution. We are committed to improving the quality of our patient's lives by offering unrivaled quality, consistency and meticulously curated products that satisfy our customers unique, individual needs. When it comes to customer service experience, our dispensaries will set a new standard of excellence, emphasizing health and wellness by a highly knowledgeable team. A team that is committed to our values, our people, and our communities; we are looking for people who are inspired by our vision and stay dedicated to our mission as we continuously expand.
EEO STATEMENT 
Ascend Wellness Holdings, Inc. ("AWH") and its subsidiaries is an equal opportunity employer and celebrate the population of differences and does not discriminate in its hiring / hiring practices, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other characteristic protected by law. 
#ENGHP

Cultivation Technician- Athol

<h3>Job Description</h3>
Job Description
Engineer Science into Impact
At EmergingDx Inc, we are reimagining diagnostics at the edge of science, engineering, and innovation. As an institution for integrated innovation, we fuse biology, technology, and systems design to build transformative diagnostic tools that improve human health and empower clinicians, patients, and communities.
We’re looking for an In Vitro Diagnostics (IVD) Scientist/Engineer to join our mission-driven team. You’ll help architect, prototype, and validate next-generation diagnostic platforms—from rapid point-of-care assays to integrated microfluidic systems for disease monitoring and early detection.
This role is ideal for someone who thrives at the intersection of biological insight and engineering ingenuity, and who wants to shape the future of healthcare from the bench to the field.
Responsibilities (What You’ll Do)
<ul>
<li>Design, develop, and optimize IVD assays (immunoassays, molecular diagnostics, or clinical chemistry) for lab-on-chip and point-of-care platforms</li>
<li>Collaborate with cross-functional teams to integrate biological assays with microfluidic, optical, and electronic systems</li>
<li>Lead analytical validation studies including sensitivity, specificity, reproducibility, and regulatory performance metrics</li>
<li>Prototype, test, and troubleshoot diagnostic systems across wet lab and hardware environments</li>
<li>Contribute to product development processes including documentation, risk analysis, quality systems (ISO 13485), and FDA regulatory pathways</li>
<li>Apply systems thinking to challenges in sample preparation, biomarker detection, signal amplification, and data analysis</li>
<li>Effectively communicate results and technical insights to clients and stakeholders through both written reports and oral presentations</li>
<li>Develop and manage fast-paced project timelines while proactively identifying and mitigating risks</li>
<li>Stay current on scientific literature, emerging technologies, and clinical needs in diagnostics</li>
<li>Craft and deliver clear, compelling narratives—both written and oral—conveying technical project progress and proposed initiatives</li>
</ul>
Qualifications (What You Bring)
<ul>
<li>PhD in Bioengineering, Molecular Biology, Chemistry, Biomedical Engineering, Chemical Engineering, or related field</li>
<li>5+ years of experience in vitro diagnostics, medical devices, or translational research</li>
<li>Strong knowledge of assay formats: ELISA, lateral flow, qPCR, CRISPR-based diagnostics, isothermal amplification, or electrochemical detection</li>
<li>Experience with fluidic handling systems (manual and automated), sample matrices (blood, saliva, urine), and surface functionalization</li>
<li>Familiarity with data acquisition and analysis, including use of MATLAB, Python, or other statistical tools</li>
<li>Comfortable working across disciplines with engineers, designers, and clinicians</li>
<li>Adaptability in fast-paced environments</li>
<li>Detail-oriented, systems-focused, and passionate about delivering health impact through innovation</li>
<li>Proven track record of leading R&amp;D programs to deliver innovative, high-quality outcomes on schedule, aligned with stakeholder expectations and technical goals</li>
<li>Excellent verbal and written communication skills</li>
<li>Bonus: Experience in microfabrication, biosensor integration, point-of-care regulatory submissions, or multiplexed assay development</li>
</ul>
Why EmergingDx
<ul>
<li>You’ll work on products, platforms, and ventures — not just features</li>
<li>You’ll gain ownership, mentorship, and momentum</li>
<li>You’ll be part of something bigger: a community shaping what’s next</li>
<li>We offer a competitive salary with full benefits package.</li>
</ul>
Ready to redefine diagnostics? Send your resume to <a href="mailto:careers@emergingdx.com" target="_blank">careers@emergingdx.com</a>
Subject: In Vitro Diagnostics Scientist/Engineer – [Your Name]
Due to the nature of our business and information associated with this position, interested candidates must be US Citizens or Permanent Resident.
At EmergingDx Inc, we are proud to be an Equal Opportunity Employer committed to building and sustaining a talented, inclusive, and diverse workforce. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, marital status, national origin, age, veteran status, disability, or any other legally protected status.
Note to recruiters: We are not seeking assistance for this position. Please do not contact us via phone or email regarding this opening.
As a U.S. Government contractor, we are required to collect certain applicant information for federal reporting purposes.

In Vitro Diagnostics Scientist/Engineer - Redefine Diagnostics

<h3>Job Description</h3>
Job DescriptionSalary: 
Job Title: Research Assistant
Job Location: Watertown, MA
About Piton Therapeutics
Piton Therapeutics is located in Watertown, Massachusetts. The company utilizes its proprietary AI Drug Discovery System to efficiently choose drug candidates that precisely target biological processes in the gut microbiome and validate their performance in-house. Piton offers competitive salary and benefits packages for employees and provides an unparalleled working environment.
Position Summary:
Piton is seeking a motivated, collaborative, and experienced research assistant with extensive experience in one or more of the following areas: molecular biology, microbiology, enzyme assays, and cell culture handling. Working under direct supervision of the Principal Scientist, the Research Associate will perform a variety of routine experimental protocols and procedures to support the objectives of the drug candidate development at Piton. Candidates are expected to work in a flexible, fast-paced environment with a diverse team.
Responsibilities:
<ul>
<li>Performs a variety of routine laboratory tasks and procedures.</li>
<li>Maintains and propagates established mammalian cell lines.</li>
<li>Maintains the bacterial culture collection and conducts in-vitro co-culture experiments.</li>
<li>Prepares and maintains stocks of necessary reagents, solutions, and supplies.</li>
<li>Cultivates aerobic and anaerobic bacteria from human tissues, creates bacterial stocks, and revives bacteria as needed.</li>
<li>Performs ELISAs.</li>
<li>Cell-based assay development.</li>
<li>Performs data analysis and presents it to small and large teams.</li>
<li>Attends team meetings to share results and contribute to experimental planning.</li>
<li>Have excellent personal task management skills and a high level of self-motivation.</li>
</ul>
Requirements:
<ul>
<li>B.S with 3-5 years or M.S. with 1-2 years of industry experience in basic laboratory techniques.</li>
<li>Experience with handling bacteria and mammalian cell lines.</li>
<li>Excellent teamwork, collaboration, and project management skills.</li>
<li>Outstanding written and verbal communication skills.</li>
<li>Self-directed, innovative, and creative thinker.</li>
</ul>
More About the Position:
Piton offers a competitive compensation and benefits package, annual bonus potential, superior opportunities for career growth and development, and a work environment that is truly collaborative, collegial, and fun.
Statement of Equal Employment Opportunity:
Piton is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, gender identity or expression, national origin and ancestry, disability, genetic information, pregnancy, veteran status, or any other protected characteristic as outlined by federal, state, or local laws.
This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, and benefits. Training and apprenticeship. Piton makes hiring decisions based solely on qualifications, merit, and business needs at the time.
Apply Today. Wed love to hear from you.
 
Note to Employment Agencies: Please DO NOT forward any agency resumes. The company WILL NOT be responsible for any unsolicited fees related to resumes.

Research Assistant

<h3>Job Description</h3>
Job Description
Duties:
<ul>
<li>Perform routine and non-routine analytical and/or microbiological assays to support raw materials, in-process samples, product release, and stability studies, following established SOPs</li>
<li>Maintain up-to-date training records, adhere to the testing schedule, and ensure the timely completion of all assignments to support the seamless operation of QC activities</li>
<li>Assist in the maintenance of laboratory equipment and inventory, including the preparation of reagents and samples to ensure smooth laboratory operations</li>
</ul>
Qualifications:
<ul>
<li>B.S. in chemistry, biology, or biochemistry, or related scientific field</li>
<li>Pharmaceutical/Biotech industry experience with 4 years in a GMP Quality Control function or equivalent, relevant industry experience</li>
<li>Experience in wet/analytical chemistry techniques including HPLC/UPLC/GC/MS/FTIR/UV-Vis&nbsp;</li>
<li>Experience in method transfer and/or analytical method implementation; solid understanding of method lifecycle management and phase-appropriate approach is desirable</li>
<li>Proficiency in LabWare LIMS, Excel, Word, and PowerPoint preferred</li>
</ul>
Company DescriptionR&amp;D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire &amp; outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL. The cornerstone of our success: a knowledgeable and experienced recruiting team. Our life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&amp;D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities. 
<h3>Company Description</h3>
R&amp;D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire &amp; outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL.\r\n\r\nThe cornerstone of our success: a knowledgeable and experienced recruiting team.\r\n\r\nOur life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&amp;D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities.

QC Analyst III (Chemist)

<h3>Job Description</h3>
Jog Title: Chromatography Principal Scientist
<ul>
<li>Location: Cambridge, MA</li>
</ul>
About the Job
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Sanofi is seeking a highly motivated individual to join our analytical group as a Chromatography Principal Scientist. The group is part of the synthetic platform within Global CMC Development that is striving to become an industry leader in the development of transformative medicines. &nbsp;&nbsp;
The primary responsibility of this position is to provide analytical support to the chemistry teams and to develop analytical methods using equipment including HPLC, UHPLC, GC, and potentiometry.
Key Responsibilities 
<ul>
<li>
Develop specific and robust analytical methods using equipment including HPLC, UHPLC, GC, TLC, and potentiometry and be responsible for validating the methods when necessary
</li>
<li>
Analyze synthetic molecules mainly by HPLC/UHPLC, GC, potentiometry, and TLC.
</li>
<li>
Perform quantification of impurities
</li>
<li>
Perform mass balance studies
</li>
<li>
Design and implement analytical strategies for synthesis intermediates and raw materials
</li>
<li>
Develop effective collaborations with others within project teams and between analytical groups
</li>
<li>
Generate technical reports independently
</li>
<li>
Share knowledge and experience of analytical method development for synthetic molecules
</li>
<li>
Introduce innovative analytical approaches to facilitate optimal decision-making.
</li>
<li>
May serve as a project lead
</li>
</ul>
About you
Basic Qualifications 
<ul>
<li>
A Masters degree or equivalent in Analytical Chemistry or related field with a minimum of 4 years of experience in the pharmaceutical/biotech industry. A PhD in Analytical Chemistry is preferred.
</li>
<li>
Expertise in the operation of LC and GC
</li>
<li>
Familiarity with the operation of potentiometry titrator, and TLC from multiple manufacturers
</li>
<li>
Extensive experiences in method development using HPLC/UPLC and GC
</li>
<li>
Experiences in analytical method validation
</li>
<li>
Record of adhering to and promoting lab safety practices
</li>
<li>
Good communications skills
</li>
</ul>
Preferred Qualifications
<ul>
<li>
In-depth understanding of the separation principles of LC and GC
</li>
<li>
Deep expertise in chromatography method development and trouble shoots
</li>
<li>
Knowledge of QbD concepts, specification setting, and cGMP, with experience in contributing to regulatory submission
</li>
<li>
Communicates effectively in individual and group settings and collaborate effectively in a multi-disciplinary team setting
</li>
<li>
Demonstrated project management skills
</li>
<li>
Consistent record of collaboration with scientists and other stakeholders at external enterprises
</li>
<li>
Advanced scientific network in the industry and academia
</li>
<li>
Record of patents and publications
</li>
</ul>
Why Choose Us? 
<ul>
<li>
Bring the miracles of science to life alongside a supportive, future-focused team.
</li>
<li>
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
</li>
<li>
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
</li>
<li>
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
</li>
</ul>
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
#GD-SA #LI-SA​ #LI-Onsite
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

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