Sr. Scientist, Downstream Process Development

ProBio; Pennington (NJ); On-site; USD 120,000 - 170,000; Full time

Benefits offered by this job

Medical, dental, and vision insurance

401(k) with company match

Parental leave

Generous PTO

FSA/HSA & life/AD&D

Commuter benefits

Wellbeing programs

Job summary

GenScript USA Inc./ProBio Inc. is seeking a skilled downstream process development scientist to translate research into GMP-compatible manufacturing for viral vector processes.

The role involves developing, scaling, and evaluating technology transfer of LVV/AAV workflows, with opportunities to lead a small team as needed. The candidate should have extensive bench experience in bioprocessing, strong DOE/statistics skills, and a track record in regulatory CMC contexts.

Qualifications

• Advanced degree (M.S./Ph.D.) in biotech-related field with 5+ years industry experience.
• Experience with LVV and AAV process development is a plus.
• Strong understanding of process scale-up, DOE, and statistical analysis.
• Experience in regulatory CMC affairs for FDA/EMA is a plus.
• Ability to lead translation to GMP manufacturing and potentially lead a small team.

Responsibilities

• Hands-on development and optimization of downstream unit operations (TFF, chromatography, viral clearance, filtration).
• Plan and execute LVV/AAV purification experiments; analyze and report data.
• Collaborate with internal/external partners to evaluate new bioprocessing techs.
• Support process transfer, cGMP risk evaluation, and deviation management with cross-functional teams.
• Maintain detailed project timelines and documentation.
• Prepare CMC sections for regulatory submissions and progress reports.
• Present updates to management on process development and manufacturing support activities.
• Read literature to generate ideas for process design and development.
• Perform other duties as assigned.

Skills

DOE & stats

Communication

Independent work

Documentation

Team collaboration

Education

Master’s or PhD in biotech/related field

Job description

Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation in biotechnology and healthcare by providing researchers and companies with the building blocks needed to develop groundbreaking treatments and products. Guided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions.

About ProBio:

ProBio, a subsidiary of GenScript, is a global CDMO offering end-to-end services from discovery to GMP for plasmids, antibodies, and cell & gene therapies. We bring together multidisciplinary expertise to accelerate development and manufacturing through customized, and comprehensive services. ProBio has established companies in the United States, the Netherlands, South Korea, and China (Hong Kong, Shanghai, and Nanjing) and other regions to serve global customers, and has helped customers in the United States, Europe, Asia Pacific and other regions obtain more than 150 IND approvals since October 2017.

Position Overview:

The position reports to the Associate Director, Downstream Viral Vector Process Development & MSAT Department. This role is ideally suited for a dynamic bench-focused individual to support/lead translation of research process to GMP-compliant manufacturing, and will develop, scale-up, and evaluate the technology transfer of viral vector processes. This is a great opportunity to join a fast-paced company, develop, and expand technical expertise to lead by example and potentially lead a small team in the near future.

Responsibilities:

• Hands-on experimental work in the development and optimization of downstream unit operations (TFF, Affinity/Ion Exchange/multimodal Chromatography, Viral clearance, Sterile filtration, etc.) for viral vector manufacturing process.
• Contribute to the planning, design, and execution of AAV/LVV purification-related experiments to analyze, interpret, and report data summary packages.
• Interact and collaborate with internal/external partnerships to evaluate and implement new bioprocessing technologies and strategies.
• Interact with cross functional teams (Analytic team, MFG, Supply chain, Facility, QA, QC) to support process technology transfer, cGMP risk evaluation, and deviation management.
• Maintain and follow detailed and comprehensive project timelines.
• Support in the preparation of CMC sections for regulatory submissions (IND, Annual Reports, and BLA), invention disclosures, progress reports, and publications.
• Present updates to project or upper management teams on process development and manufacturing support activities.
• Read and understand scientific literature in gene and cell therapy. Use the knowledge to generate ideas and contribute to process design and development.
• Perform other duties as assigned based on business needs.

Qualifications:

• Master’s or Ph.D. degree with 5+ years’ relevant industry experience in Chemical/Biochemical Engineering, Biological Sciences, or a related scientific discipline in biotech development with particular experience in gene and cell therapy product design. Experience with LVV and AAV process development is a plus.
• Previous experience in viral vector process development and manufacturing is highly preferred.
• Strong understanding of process scale-up and scale-down modeling.
• Good understanding of Design of Experiment (DOE) and statistical analysis.
• Experience in CMC regulatory affairs for FDA, and EMA is a plus.
• Strong organizational skills and detailed documentation abilities are required.
• Work independently in hands-on laboratory setting, self-motivated to learn and develop new techniques.
• Strong interpersonal, verbal, and written communication skills.
• Results oriented, be able to effectively prioritize and complete tasks on time.
• Collaboration and teamwork.

• Benefits include medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one
• paid parental leave after just three (3) months of employment
• paid time off policy that includes vacation time, personal time, sick time, floating holidays, and company holidays
• flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance
• commuter benefits, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.

GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.

GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.

Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.