Sr. Scientist, Downstream Process Development
GenScript/ProBio · United States
Posted 26 days ago · $100k - $130k
or apply directly on GenScript/ProBio's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 26 days GenScript/ProBio's roles stay open a median of 45 days
- Reposted
- No
- Salary listed
- Yes 54% of GenScript/ProBio's roles list one
- Ghost-job risk at GenScript/ProBio
- high 53 stale, 2 reposted of 82 open
- Hiring momentum
- 117 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-09-17
Measured from postings appearing on and disappearing from GenScript/ProBio's own greenhouse board since 2026-08-03. Full hiring picture for GenScript/ProBio.
About this role
The Sr. Scientist in Downstream Process Development will focus on hands-on experimental work to develop and optimize downstream unit operations for viral vector manufacturing. This role involves planning and executing purification-related experiments, collaborating with cross-functional teams, and supporting regulatory submissions. The position also offers opportunities to lead a small team and contribute to innovative bioprocessing technologies.
- benefits
- 5/5
- freshness
- 4/5
- career value
- 4/5
- role clarity
- 4/5
- pay transparency
- 5/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of GenScript/ProBio as an employer.
What you need
- Master’s or Ph.D. degree with 5+ years’ relevant industry experience in Chemical/Biochemical Engineering, Biological Sciences, or a related scientific discipline
- Experience in viral vector process development and manufacturing
- Strong understanding of process scale-up and scale-down modeling
- Good understanding of Design of Experiment (DOE) and statistical analysis
- Strong organizational skills and detailed documentation abilities
- Ability to work independently in a hands-on laboratory setting
Nice to have
- Experience with LVV and AAV process development
- Experience in CMC regulatory affairs for FDA and EMA
What you get
- Medical, dental, and vision insurance
- 401(k) retirement plan with company match that vests fully on day one
- Paid parental leave after three months of employment
- Paid time off policy including vacation time, personal time, sick time, floating holidays, and company holidays
- Flexible spending and health savings accounts
- Life and AD&D insurance
Worth weighing
- Pay range is estimated between $100k - $130k based on skill set and experience
- Role may involve leading a small team in the future, which could be a consideration for career growth
Summarised from GenScript/ProBio's posting. Read the full original.
Listed by GenScript/ProBio on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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