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<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 focuses 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 Analytical/QC Lab Metrologist is responsible for the timely installation, maintenance, repair, calibration, and IQ/OQ of instruments, balances, and other equipment used by the Analytical Development (AD) and Quality Control (QC) groups. This role also ensures Standard Operating Procedures are technically sound and provide full regulatory compliance. This position is critical to supporting high-quality science, operational excellence, and regulatory compliance across both sites.
Core Responsibilities: 
<ul>
<li>Revises and reviews metrology-related protocols and IQ/OQ to ascertain proper functioning of the instrumentation. Ensures that appropriate documentation for the instrument calibration program is in place for compliance with regulatory expectations.</li>
<li>Schedules, executes and supports instrument calibrations and preventative maintenance in such a way so as not disrupt the analysts using the instruments. Responsible in the assignment of instrument custodians, assuring instrument maintenance and usage logbooks have been maintained. Trouble shooting or judging the issue for chromatographic systems mainly LC/GC.</li>
<li>Negotiates and manages contracts with external vendors and contracted services as required. Oversees the work of contracted personnel to install/modify equipment and systems in accordance with the specific needs of the AD and QC groups while meeting all cGMP and USP requirements.</li>
<li>Keep abreast of instrument validation requirements to ensure compliance with respect to USP and cGMP requirements.</li>
<li>Provides assistance in internal and customer audits by providing relevant, up to date documentation related to calibration, qualification and maintenance of appropriate analytical instrumentation used by the analytical groups. </li>
<li>Leads the process to evaluate, purchase and install new instrumentation. Interacts with internal and external vendors to ensure the proper instrumentation is identified to support the needs of the business. Evaluates and recommends appropriate application of new software packages as well as upgrades of software/firmware/hardware.</li>
<li>Directly involved with and supports investigations that are instrument related. Conducts all work in compliance with USP and cGMP standards and all other appropriate Federal, state and local regulations.</li>
</ul>
Qualifications: 
Required
<ul>
<li>Bachelor’s Degree in chemistry or a related science with a minimum of 5 years’ related experience </li>
<li>Familiarity with LC/GC trouble shooting.</li>
<li>Experience in a cGMP environment</li>
<li>Ability to exercise independent judgment in the application of scientific principles pertaining to analyses as related to this business and operation </li>
<li>Proficiency with computers and other software packages relevant to installation, modification, calibration and qualification of instrumentation systems and equipment</li>
<li>Strong communication skills; written and verbal. </li>
<li>Possess strong organizational skills</li>
</ul>
Preferred
<ul>
<li>Experience in lab equipment such as analytical balance, micro balance, KF, OVEN-KF, NMR, ICP-MS, PSD, XRPD, TGA, DSC, etc. </li>
<li>Experience or familiarity with Labware LIMS and the Instrument Manager module</li>
<li>Experience or familiarity with Master Control and Veeva</li>
<li>Recent relevant experience in bulk pharmaceutical/API manufacturing or specialty chemicals</li>
</ul>
Our Commitment:
<ul>
<li>Health &amp; Wellness: Comprehensive health &amp; Wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies. </li>
<li>Financial Wellness: Comprehensive total compensation package that includes competitive base salary, Defined Contribution Pension program, eligibility for performance-based bonuses, and attractive 401(k) Plan with company match.</li>
<li>Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.</li>
<li>Inclusive Culture: At Veranova, an inclusive culture is integral to our values. We are committed to ensuring that everyone can bring their full self to work and thrive in their career.</li>
</ul>
How to Apply: 
At Veranova, we are on a 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. 
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 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>
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

Analytical/Quality Control Lab Metrologist

<h3>Job Description</h3>
Job Descriptionjob summary: 
The Chemist is an individual contributor responsible for performing a variety of tests on samples within a Quality Control (QC) laboratory. This role involves operating and maintaining various instruments, ensuring data integrity, and adhering to strict cGMP and documentation practices. The specific duties and responsibilities may vary based on the assigned department, group, as well as the individual's education, training, and level of experience. This position requires a strong working knowledge of analytical techniques and equipment to ensure the quality and compliance of all tested materials. 5+ years of experience in analytical testing within a cGMP environment or a Quality Control (QC) lab is required. 
FLSA Classification: Full-Time
Work Location: Fall River, MA
Work Hours: General Shift: 8:30AM - 5:00PM (may vary based on business needs)
 location: Fall River, Massachusetts job type: Permanent salary: $90,000 - 100,000 per year work hours: 9 to 5 education: Bachelors responsibilities: 
<ul>
<li>Execute a full range of analytical testing, including routine, advanced, and critical analysis, with a working knowledge of raw materials testing and release.</li>
<li>Operate and maintain a variety of specialized instruments, such as Karl Fischer, HPLC, GC, Particle Size, and ICP, and coordinate with vendors for their installation and qualification.</li>
<li>Ensure strict compliance with all cGMP (current Good Manufacturing Practices), data integrity, and good documentation practices.</li>
<li>Lead investigation activities to address testing deviations or other issues as they arise.</li>
</ul>
 qualifications: 
Required:
<ul>
<li>Bachelor's degree (BS or BA) in scientific discipline</li>
<li> 5+ years of experience in analytical testing within a cGMP environment or a Quality Control (QC) lab </li>
</ul>
?Preferred:
<ul>
<li> Experience in Inhalation products (MDI)</li>
</ul>
 #LI-AB1 
 skills: High Pressure Liquid Chromatography (HPLC), Gas Chromatography (GC) 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

QC Chemist III

<h3>Job Description</h3>
Job DescriptionCompany Description 
The work we do at Eurofins matters, and so do our employees. At Eurofins, 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, apply with us today!&nbsp;&nbsp;
Job Description 
We are seeking a candidate that will support a client team that is responsible for developing robust and efficient purification processes of recombinant proteins and other biological therapeutics from early to late stage of development.&nbsp;
We are seeking an analytical scientist who will work in a collaborative environment to be engaged in the analysis, monitoring and characterization of in-process samples to support the client in improving process performance by optimizing product recovery and impurity removal. This role will provide routine analytical testing. Knowledge and expertise in analytical biochemical techniques including HPLC (HI-C, RP, SEC, etc.), and Octet are a must. The successful candidate must be self-motivated and able to work independently, be accountable for own results and prioritize own workflow, and seek opportunities to take on new projects.&nbsp;
Job Responsibilities and Requirements:&nbsp;
<ul>
<li>Experience with protein chemistry, protein analytics, and bioprocess technology is required&nbsp;</li>
<li>Expertise in analytical chemistry using a broad range of separation, chromatographic, spectroscopic and other detection techniques to characterize and monitor protein purification process&nbsp;</li>
<li>Hands on experience and working knowledge on techniques including but not limited to&nbsp; liquid chromatography like UPLC/HPLC (size-exclusion, hydrophobic, ion-exchange, affinity), and Octet&nbsp;</li>
<li>Hands on experience with SDS-PAGE, ELISA, and&nbsp;experience with protein purification/chromatography at the lab scale is a plus&nbsp;</li>
<li>A working knowledge on Empower and/or ChemStation control and data analysis software is strongly preferred&nbsp;</li>
<li>Work closely with colleagues by providing quality data to support product development through early clinical phases in a timely manner; uses understanding of analytical tools to assess and interpret experimental data&nbsp;</li>
<li>Maintains written records (electronic lab notebooks and databases) of all experimental work in accordance with Good Laboratory Practices&nbsp;</li>
<li>Leads in the routine calibration, maintenance, troubleshooting and repair of laboratory instruments, systems or apparatus and may interact with internal site or external vendors in the maintenance and continuous improvement of safe and effective working practices&nbsp;</li>
</ul>
Qualifications 
<ul>
<li>Bachelors or Masters Degree in Biotechnology, Biochemical Engineering, Analytical Chemistry, Chemical Engineering or other related discipline&nbsp;</li>
<li>BS + 4-6 years or MS + 2-4 years of relevant experience&nbsp;</li>
<li>Experience with HPLC (SEC, HIC, and RP), protein purification methods, and octet&nbsp;</li>
</ul>
<ul>
<li>Excellent attention to detail and ability to follow procedures to generate reproducible data in a controlled laboratory environment</li>
<li>Excellent skills in Microsoft Office, data analysis software, and other related applications</li>
<li>Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies</li>
<li>Ability to think critically and demonstrate troubleshooting/problem solving skills</li>
<li>Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
</ul>
 Additional Information 
<ul>
<li>Position is full-time, on-site Monday-Friday 8AM-5PM.&nbsp;</li>
<li>Pay range: $27.00 - $31.00 based on degree level and years of relevant experience with the skills utilized in the role.&nbsp;</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>#LI-EB1</li>
</ul>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Bioprocess Analytical Chemist (Purification Process Support)

<h3>Job Description</h3>
Job Descriptionjob summary: 
The Chemist is an individual contributor responsible for performing a variety of tests on samples within a Quality Control (QC) laboratory. This role involves operating and maintaining various instruments, ensuring data integrity, and adhering to strict cGMP and documentation practices. The specific duties and responsibilities may vary based on the assigned department, group, as well as the individual's education, training, and level of experience. This position requires a strong working knowledge of analytical techniques and equipment to ensure the quality and compliance of all tested materials. 3+ years of experience in analytical testing within a cGMP environment or a Quality Control (QC) lab is required. 
FLSA Classification: Full-Time
Work Location: Fall River, MA
Work Hours: General Shift: 8:30AM - 5:00PM (may vary based on business needs)
 location: Fall River, Massachusetts job type: Permanent salary: $70,000 - 90,000 per year work hours: 9 to 5 education: Bachelors responsibilities: 
<ul>
<li>Execute a full range of analytical testing, including routine, advanced, and critical analysis, with a working knowledge of raw materials testing and release.</li>
<li>Operate and maintain a variety of specialized instruments, such as Karl Fischer, HPLC, GC, Particle Size, and ICP, and coordinate with vendors for their installation and qualification.</li>
<li>Ensure strict compliance with all cGMP (current Good Manufacturing Practices), data integrity, and good documentation practices.</li>
<li>Lead investigation activities to address testing deviations or other issues as they arise.</li>
</ul>
 qualifications: 
Required:
<ul>
<li>Bachelor's degree (BS or BA) in scientific discipline</li>
<li> 3+ years of experience in analytical testing within a cGMP environment or a Quality Control (QC) lab </li>
</ul>
?Preferred:
<ul>
<li> Experience in Inhalation products (MDI)</li>
</ul>
 #LI-AB1 
 skills: High Pressure Liquid Chromatography (HPLC), Gas Chromatography (GC) 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

QC Chemist II

<h3>Job Description</h3>
Job DescriptionDescription:
Hoyle Tanner is seeking a part-time Geotechnical Engineer for our Ground Transportation Services Division. If you have a PE license and 10 years of experience, we would like to offer you a role in design and analysis of infrastructure projects from bridge foundations, retaining walls, treatment plan structures. A perfect opportunity for the retired Engineer who is looking for a part-time project.
We are a welcoming, collaborative, respectful, encouraging, and diverse community where you can achieve your career goals. Our midsize allows you to be visible and heard. Hoyle Tanner offers you a flexible schedule, remote work opportunities and a generous sign-on bonus. See our impressive benefits package for more information.
 
Location: Manchester, NH
Manchester’s historic mill yard, our 30,000 square foot office space sits perched on the 5th floor of the original Amory Mill and is the home of our company’s headquarters. Remnants of the historic charm remain in various locations throughout the mill, while our space has been redesigned with modern lines and architectural accents. 
 
Job Responsibilities:
<ul>
<li>Develop geotechnical investigation requirements for projects and develop scopes of services and budgets for sub-consultant partners including other geotechnical specialists or subsurface investigation companies</li>
<li>Interface with sub-consultant geotechnical engineering firms or subsurface investigation companies to coordinate services and review submissions</li>
<li>Perform fieldwork, as necessary, to subsurface investigation parameters or to observe investigations</li>
<li>Perform/ review design calculations for project components such as abutments, walls, foundations, retaining walls, and tanks</li>
<li>Assist with design of airfield pavements and present alternative pavement solutions that may provide project sustainability and resilience benefits</li>
<li>Mentor team members on aspects of geotechnical engineering including interpretation of subsurface data and designs of civil infrastructure components</li>
<li>Design and evaluate shallow and deep foundation systems including driven piles, micro-piles, integral abutments, reinforced earth structures, and other geotechnical engineering solutions</li>
<li>Prepare geotechnical reports, design calculations, and construction specifications</li>
<li>Collaborate with project managers and other technical team members to ensure the successful completion of projects by communicating the integration of geotechnical investigations into design projects</li>
<li>Perform site visits and inspections to assess soil conditions, evaluate foundation performance, and provide recommendations for rehabilitation</li>
<li>Stay current with industry standards, codes, and regulations related to geotechnical engineering</li>
<li>Participate in project meetings and communicate effectively with clients, contractors, and regulatory agencies</li>
</ul>
Benefits:
<ul>
<li>Competitive salary aligning with experience</li>
<li>Flexible hours and opportunity for a hybrid work environment</li>
<li>Flexibility to work part or full time</li>
<li>Opportunities for professional development and continuing education</li>
<li>Comprehensive benefits package including health insurance, retirement plans and paid time off</li>
<li>Collaborative and supportive work environment</li>
</ul>
Requirements:
Qualifications:
<ul>
<li>BS in Civil Engineering (MS in Geotechnical Engineering preferred)</li>
<li>Professional Engineer (PE) licensure required</li>
<li>Minimum of 10 years' experience in geotechnical engineering, with a focus on the design of bridge foundations, retaining walls, treatment plant structures, and/ or facility foundations</li>
<li>Proficiency in the design and analysis of shallow and deep foundations including driven piles, micro-piles, integral abutments, and reinforced earth structures</li>
<li>Strong understanding of geotechnical engineering principles, soil mechanics, and foundation design</li>
<li>Experience with related geotechnical software, such as LPile, or other similar tools and industry-related applications</li>
<li>Strong communication and interpersonal skills, with the ability to work effectively in a team environment as well as the ability to work independently</li>
<li>Strong problem-solving skills and attention to detail</li>
<li>Salary is contingent on experience</li>
</ul>
Hoyle Tanner is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Hoyle Tanner does not currently offer sponsorship and participates in E-Verify. All offers are contingent upon a successful criminal background check.

Geotechnical Engineer - Manchester, NH

<h3>Job Description</h3>
Job Description
We are currently seeking a Lead Scientist / Engineer with a PhD in Systems &amp; Control, Biomedical Engineering, Applied Mathematics, or a related quantitative field, and 5–6+ years of experience in applied modeling and estimation. This role will function as a senior member of the company’s algorithm team. It will involve designing and implementing Etiometry’s next-generation physiologic risk and treatment-prediction algorithms. The position will require close collaboration with Etiometry’s data science, product, and clinical teams to translate physiologic and clinical requirements into real-time decision support tools deployed in the ICU.
Responsibilities
<ul>
<li>
Lead the design, implementation, and validation of algorithms that predict patient trajectories and responses to interventions (e.g., fluids, vasoactives, ventilator changes).
</li>
<li>
Extend Etiometry’s existing ODE-based physiologic models with advanced estimation methods (e.g., Kalman filters, Bayesian inference, particle filters).
</li>
<li>
Integrate data-driven approaches (e.g., neural networks, probabilistic ML, hybrid mechanistic/ML frameworks) with classical physiology-based models.
</li>
<li>
Translate physiologic and clinical requirements into quantitative risk indices for FDA-regulated software.
</li>
<li>
Work with real-world ICU data, including physiologic waveforms, vital signs, and laboratory values.
</li>
<li>
Mentor junior scientists and collaborate with engineers, clinical experts, and regulatory affairs to bring models from research → cleared product.
</li>
</ul>
Basic Qualifications
<ul>
<li>
PhD in Systems &amp; Control, Biomedical Engineering, Applied Mathematics, Electrical/Mechanical Engineering, or a related field.
</li>
<li>
5–6+ years of experience (industry or postdoctoral) in applied modeling, estimation, or control systems.
</li>
<li>
Strong background in dynamical systems &amp; ODE/PDE modeling.
</li>
<li>
Strong background in state estimation techniques (Kalman filters, stochastic processes, Bayesian methods).
</li>
<li>
Working knowledge of machine learning (neural networks, probabilistic ML, data-driven system identification).
</li>
<li>
Proficiency in scientific computing in Python (NumPy, SciPy, PyTorch, TensorFlow).
</li>
<li>
Strong communication and organization skills.
</li>
<li>
Proven ability to work in cross-disciplinary teams and translate theory into applied solutions.
</li>
</ul>
Desired Qualifications
<ul>
<li>
Experience working with clinical monitoring data (ICU waveforms, vital signs, laboratory data, EHR integration).
</li>
<li>
Familiarity with computational physiology or biomedical modeling.
</li>
<li>
Knowledge of medical device software lifecycle (IEC 62304, FDA 510(k)).
</li>
<li>
Experience mentoring junior scientists or leading research projects.
</li>
</ul>
About Etiometry
Etiometry is the market leader in predictive analytics for the Intensive Care Unit. Our system leverages real-time patient data to provide clinicians with actionable information that improves care for the most vulnerable patients. In use at some of the best medical institutions across three continents, the Etiometry Platform has a proven track record in improving outcomes while reducing hospital costs. Our next generation of algorithms will go beyond monitoring risk to forecasting how treatments will affect patient physiology — giving clinicians foresight to guide critical interventions. By joining Etiometry, you will be at the forefront of clinical innovation, working with a passionate team of engineers and scientists with the mission of transforming the delivery of critical care. You will become an integral part of a dynamic team whose work will directly impact patients worldwide and shape the future of ICU analytics.

Lead Algorithm Scientist Engineer

<h3>Job Description</h3>
Job DescriptionCompany Description 
About Mote Therapeutics
Are you a scientific leader with a passion for advancing RNA therapeutics and the drive to make a difference in the world? Do you want to be a part of a dynamic and innovative team at the forefront of RNA medicines? If so, join our new RNA Venture and be a part of the revolution in RNA therapeutics!
Backed by Fapon Biotech, an international leader in in vitro diagnostics, biologics, and precision medicines, Mote Therapeutics is an innovative Lexington-based biotechnology startup building the RNA medicines of tomorrow. Led by a pioneer in the field of RNA therapeutics and supported by Fapon’s Greater Boston R&amp;D Center of Excellence, we’re pulling together a team of talented scientists, leaders, and operations specialists to solve some of the major barriers to success that RNA therapeutics face.
About Fapon Biotech
Founded in 2001 and headquartered in Guangdong, China, Fapon Group is mainly engaged in product R&amp;D and services of in vitro diagnostics (IVD), biological therapies, and precision diagnostics and treatments. With our core value of "foresee and prepare for what the future demands", Fapon has historically focused on three major businesses: raw material solutions, IVD ecosystem platform service, and intelligent digital diagnosis and treatment. Fapon’s recent expansion into therapeutics was recently marked by success with the receipt of IND approval from the FDA for a differentiated CD47 antibody drug, the first in a rapidly expanding therapeutics effort.
With a global footprint, Fapon has established major production and sales (R&amp;D) bases in Beijing, Shenzhen, Shanghai, the United States, Germany, India and other locations throughout the world, forming a global R&amp;D, production, marketing, and service network with products being widely sold in 61 countries and regions.
You can learn more about us by visiting <a href="https://en.faponbiotech.com" target="_blank">https://en.faponbiotech.com</a>
An equal-opportunity employer, Fapon welcomes and encourages diversity in our workforce.
Job Description 
We are seeking a scientific contributor to develop validated analytical assays for LNP and drug product characterization. This role will be responsible for designing, developing and validating analytical assays for a targeted LNP drug product to support the platform and pipeline development. The candidate would have the opportunity to work in a collaboration-oriented role in which they would coordinate with other teams and provide analytical support to the discovery and PD teams. The ideal candidate is a sciences major with strong exposure to analytical techniques and who is excited by the idea of being a core participant in building an early startup and guiding the scientific vision of the company. They would be engaged in science and driven by our mission to create therapies that help people in ways that are currently impossible.
<ul>
<li>Designing, developing and validating analytical assays for LNP and targeted LNP drug product characterization</li>
<li>Develop assays for LNPs including lipid raw material QC, composition assessment, Lipid/cargo profiling and LNP/tLNP characterization using HPLC (SEC, Reverse Phase), fluorescence-based methods and other analytical techniques</li>
<li>Work with cross-functional groups including LNP discovery, PD and CMC team to support needs of analytical method development, characterization, and transfer</li>
<li>Perform CRO outreach including experimental planning, work coordination and data interpretation for as analytical SME</li>
<li>Support technology transfer to Industry Partners</li>
<li>Foster collaborative relationships across the team and company and engage in a positive and exciting work environment</li>
<li>Contribute to hiring, training, and collaborating with scientists (as needed)</li>
<li>Author technical documents, including SOPs for analytical methods, maintain diligent records and demonstrate proficiency in scientific communication</li>
<li>Support high-quality documentations to support regulatory filings</li>
</ul>
Qualifications 
Minimum Qualifications:
<ul>
<li>BS/MS in life sciences, pharmaceutical sciences, or related field, preferably with 7/5 years of relevant experience. The title will be commensurate with experience.</li>
<li>Hands on experience developing analytical methods for complex biological therapeutics</li>
<li>Prior experience in developing analytical methods for LNP characterization is a must and will be key for this role</li>
<li>Knowledge of ICH/USP guidelines</li>
<li>Experience in analytical methods with HPLC (IPRP, SEC, IEx), UV-vis, colorimetric and fluorescence-based</li>
<li>Must be eligible to work in the United States</li>
</ul>
&nbsp; Preferred Qualifications:
<ul>
<li>Experience in developing validated analytical assays</li>
<li>Experience in advanced analytical methods for LNP characterization such as LC-MS, MALS, SEC-MALS etc</li>
<li>Strong communication skills and ability to present complex technical topics to diverse audiences with varying technical depth.</li>
<li>Strong collaborative instinct with good time and resource management skills to match the fast-paced start-up work culture.</li>
<li>Able to collaborate on and execute multiple parallel studies</li>
</ul>
 Additional Information 
What We Offer:
At our RNA Venture, we aim to outmatch the typical benefits you might see in an early startup. We offer:
<ul>
<li>Financial security through competitive compensation, incentives, and retirement plan</li>
<li>Health care and well-being programs including competitive medical, dental, vision &amp; medical benefits</li>
<li>Generous paid time off including vacation, sick time, holidays, and winter shutdown</li>
<li>401(k) retirement savings with a generous company match</li>
<li>Commuter benefits</li>
<li>Other comprehensive voluntary benefits include but are not limited to pet insurance, life insurance, employee assistance program (EAP), discount programs, and many more</li>
<li>We continue to optimize our benefits &amp; wellness programs as we grow our organization to make sure they meet our diverse workforce needs</li>
<li>The stability of a startup backed by a company with a record of strong financial performance year over year</li>
</ul>

Senior/Principal Research Associate (LNP Analytics)

<h3>Job Description</h3>
Job DescriptionContract Research Associate – Virology (contract 3-4 months) &nbsp;Why Work for Us?At Candel, our people drive our success. We value diversity, collaboration, and bold thinking in a supportive, mission-driven environment. We are a high performing team, showing up for each other and stay focused on making a difference for patients and families. Our leadership is transparent and empowering, and our culture is built on trust, flexibility, and accountability, encouraging ownership and innovation every day.Our Science: Advancing Cancer ImmunotherapiesCandel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses. Our platforms use genetically modified adenovirus and HSV constructs. With positive Phase 3 results for our lead candidate, it’s an exciting time to join us and help bring transformative cancer treatments to patients. Learn more: <a href="http://www.candeltx.com" target="_blank">www.candeltx.com</a>Position Summary:We are seeking a highly motivated and collaborative Research Associate with a strong foundation in virology to support the development of next-generation HSV-1 viral immunotherapy candidates. This individual will contribute to the enLIGHTEN™ Discovery Platform through hands-on experimental work, including viral vector testing, mammalian cell culture, and virology-specific assays. The ideal candidate will bring a passion for innovation and a desire to work in a fast-paced, cross-functional research environment.Key Responsibilities:
<ul>
<li>Support the design, production, and testing of novel HSV-based viral vectors.</li>
<li>Conduct classical virology techniques such as virus production, purification (e.g., ultracentrifugation), and titering.</li>
<li>Execute virology-specific assays including plaque assays, TCID50, viral titration, and viral genome quantification using qPCR.</li>
<li>Contribute to viral vector engineering and optimization of workflows.</li>
<li>Maintain mammalian cell culture operations, including cryopreservation, routine culture, and cell banking.</li>
<li>Perform in vitro to evaluate viral vector transduction and biological activity.</li>
<li>Document experiments in electronic laboratory notebooks, analyze data, and prepare reports for internal review.</li>
<li>Contribute to a scientific culture that values creativity, rigor, and innovation.</li>
</ul>
Qualifications:Education:
<ul>
<li>MS in Virology, Biotechnology, or related field with 1–3 years of industry experience, or</li>
<li>BS with 3–5 years of relevant experience.</li>
</ul>
Experience and Skills:
<ul>
<li>Hands-on experience with virus production, purification, and quantification techniques (e.g., plaque assays, TCID50, qPCR) required.</li>
<li>Solid foundation in mammalian cell culture and aseptic technique.</li>
<li>Familiarity with viral vector design and characterization, particularly HSV-based systems.</li>
<li>Strong analytical and organizational skills with attention to detail.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Proficiency in Microsoft Office, GraphPad Prism, and SnapGene (preferred).</li>
</ul>
&nbsp;Work Environment:This is a lab-based position in Needham, Massachusetts. &nbsp;
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Contract Research Associate - Virology

<h3>Job Description</h3>
Job DescriptionJob Title: Analytical Chemist Job Description
We are seeking an analytical chemist to support, lead, and develop the R&amp;D team in creating innovative new products. This role involves performing field testing, scaling up processes, and developing new polymers, adhesives, epoxies, and coatings.
Responsibilities
<ul>
<li>Lead the R&amp;D team in developing new products and processes.</li>
<li>Perform field testing and scale-up of new product developments.</li>
<li>Support the development of new polymers, adhesives, epoxies, and coatings.</li>
<li>Drive all R&amp;D activities and determine new products for the marketplace.</li>
<li>Manage product development projects and drive continuous improvement activities.</li>
</ul>
Essential Skills
<ul>
<li>Strong knowledge of analytical chemistry and polymer chemistry.</li>
<li>Expertise in research and development, scale-up, and raw material testing.</li>
<li>Experience in epoxy, polymer, and adhesive development.</li>
<li>Proven track record in leading R&amp;D teams and managing product development projects.</li>
<li>5+ years of experience in R&amp;D for coatings, adhesives, and regulatory standards.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Masters or PhD in Chemistry, Materials Science, or Chemical Engineering.</li>
<li>Knowledge of regulatory standards related to coatings and adhesives.</li>
</ul>
Work Environment
The position is 100% onsite at the Westwood facility, working Monday to Friday from 9:00 am to 5:00 pm. The production schedule is 7:00 am to 3:00 pm, allowing for alignment with this schedule.
Job Type &amp; Location
This is a Permanent position based out of Westwood, Massachusetts.
Pay and Benefits
The pay range for this position is $125000.00 - $140000.00/yr.
They have full vision, dental, health, and vacation. They have great benefits for medical leave as well.
Workplace Type
This is a fully onsite position in Westwood,MA.
Application Deadline
This position is anticipated to close on Oct 2, 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.

Analytical Chemist

<h3>Job Description</h3>
Job Description
This is a position within Keller Executive Search and not with one of its clients. As the Senior Research Manager in Boston, MA, this senior role is accountable for shaping research strategy and delivering measurable outcomes across the business. The position partners closely with cross‑functional leaders, drives operational excellence, and scales processes to support growth. Key Responsibilities:
<ul>
<li>Set a clear multi‑year strategy and translate it into quarterly plans with accountable metrics.</li>
<li>Lead teams with a focus on coaching, psychological safety, and high performance.</li>
<li>Develop repeatable research frameworks and knowledge assets for decision support.</li>
<li>Build data‑driven operating rhythms, dashboards, and continuous‑improvement loops.</li>
<li>Own budgets and vendor relationships; negotiate contracts that balance value, risk, and speed.</li>
<li>Design compliant processes aligned to local regulations and internal policies.</li>
<li>Partner with Sales, Marketing, and People Operations to execute company priorities.</li>
<li>Represent the function to senior leadership; prepare crisp updates and decision memos.</li>
</ul>
To learn more about Keller, please see: <a href="https://www.kellerexecutivesearch.com/executive-recruiters-headhunters-worcester-and-springfield-massachusetts/" target="_blank">https://www.kellerexecutivesearch.com/executive-recruiters-headhunters-…</a>
Requirements
<ul>
<li>7+ years in progressively senior roles within the relevant discipline; experience leading managers.</li>
<li>Demonstrated success building scalable processes and delivering against OKRs.</li>
<li>Strong analytical and financial acumen; fluency with data tools and business cases.</li>
<li>Excellent stakeholder management and executive communication skills.</li>
<li>Working knowledge of applicable local laws, standards, and industry best practices.</li>
<li>Bachelor’s degree required; advanced degree or certifications are advantageous.</li>
</ul>
Benefits
<ul>
<li>Competitive compensation: $ 150,000–183,000 USD</li>
<li>Opportunities for professional growth and leadership development.</li>
<li>Company culture: Flat management structure with direct access to decision‑makers; open communication environment.</li>
<li>Full medical coverage.</li>
</ul>
Equal Employment Opportunity Statement: Keller Executive Search provides equal employment opportunities to all qualified applicants and employees. Employment decisions are based on merit, qualifications, and business needs, without regard to protected characteristics under applicable law. Commitment to Diversity: An inclusive and equitable workplace is actively fostered. Hiring, development, and advancement practices are designed to broaden representation and ensure fair access to opportunity. Data Protection and Privacy: Personal data is processed solely for recruitment and employment purposes, in accordance with applicable data‑protection laws (including GDPR where relevant). Information may be retained for compliance and legitimate interests, subject to data minimization and security controls. Pay Equity: Compensation practices are reviewed to support pay equity for substantially similar work, accounting for bona fide factors such as experience, education, and performance. Health and Safety: Workplace health and safety obligations are observed in line with applicable national and local requirements. Employees are expected to follow all safety policies and promptly report hazards. Compliance with Law: All recruitment, selection, and employment practices are conducted in compliance with applicable laws and regulations in the jurisdiction of employment. 
Note: This job posting may be for a position with Keller Executive Search or one of our clients. The specific employer will be identified during the application and interview process. Employment laws and requirements may vary depending on the employer and location.

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