Associate Scientist- Process Dev. Downstream and Formulation
Precigen
July 02, 2026
On-site
Germantown, MD
Operations
Associate Scientist – Process Development Downstream and Formulation
Duties and Responsibilities:
- Perform hands-on work executing downstream vector purification experiments using ultracentrifuges, chromatography systems, and tangential flow filtration (TFF).
- Support formulation development activities, including excipient screening, stability studies, and commercial in-use conditions for adenovector products.
- Perform analytical assays including HPLC, DLS, ELISA, and SDS-PAGE.
- Document study results in notebooks, forms, and technical reports.
- Communicate and present scientific findings in process development groups.
Education and Experience / Qualifications:
- BS or MS in Chemical Engineering, Biotechnology, or another relevant engineering/scientific qualification (level based on education and experience).
- Minimum 3+ years of hands-on laboratory experience in downstream purification or drug product development.
- Strong computer skills (Microsoft Office) and ability to learn new applications.
- Experience summarizing and presenting data and authoring technical reports.
Desired Key Competencies / Skills:
- Critical thinking with strong quantitative and analytical skills.
- Meticulous, self-organized, detail-oriented hands-on work habits.
- Excellent interpersonal, verbal, and written communication skills.
- Ability to understand and execute the company’s mission and values; maintain high ethical standards.
- Ability to think and adapt in a rapidly changing environment.
Working Conditions/Physical Requirements:
- Lift/carry/push/pull up to 40 pounds.
- May work with hazardous materials.
- Stand up to 4 hours at a time.
Duties and Responsibilities:
- Perform hands-on work executing downstream vector purification experiments using ultracentrifuges, chromatography systems, and tangential flow filtration (TFF).
- Support formulation development activities, including excipient screening, stability studies, and commercial in-use conditions for adenovector products.
- Perform analytical assays including HPLC, DLS, ELISA, and SDS-PAGE.
- Document study results in notebooks, forms, and technical reports.
- Communicate and present scientific findings in process development groups.
Education and Experience / Qualifications:
- BS or MS in Chemical Engineering, Biotechnology, or another relevant engineering/scientific qualification (level based on education and experience).
- Minimum 3+ years of hands-on laboratory experience in downstream purification or drug product development.
- Strong computer skills (Microsoft Office) and ability to learn new applications.
- Experience summarizing and presenting data and authoring technical reports.
Desired Key Competencies / Skills:
- Critical thinking with strong quantitative and analytical skills.
- Meticulous, self-organized, detail-oriented hands-on work habits.
- Excellent interpersonal, verbal, and written communication skills.
- Ability to understand and execute the company’s mission and values; maintain high ethical standards.
- Ability to think and adapt in a rapidly changing environment.
Working Conditions/Physical Requirements:
- Lift/carry/push/pull up to 40 pounds.
- May work with hazardous materials.
- Stand up to 4 hours at a time.