More jobs:
Research Associate, Research Scientist, Research Assistant/Associate
Job in
Westborough, Worcester County, Massachusetts, 01581, USA
Listed on 2026-07-20
Listing for:
Spectraforce Technologies
Full Time
position Listed on 2026-07-20
Job specializations:
-
Research/Development
Research Scientist, Research Assistant/Associate
Job Description & How to Apply Below
United States, Massachusetts, Westborough
Jul 16, 2026
Position Title:
Research Associate
Work Location:
Westborough, MA 01581
Assignment Duration: 3 months
Position SummaryWe are seeking a highly motivated Research Associate to support the development of cell therapy products, with a primary focus on formulation and process development.
Background & ContextThe successful candidate will contribute to development work on drug product, such as formulation design, manufacturing process development, product characterization, and evaluation of administration method.
Key Responsibilities- Support formulation development for cell therapy products, including process optimization and product evaluation.
- Conduct cell-based experiments in a laboratory setting under supervision.
- Perform basic cell culture and aseptic techniques within a biosafety cabinet (BSC).
- Assist with formulation, analytical, and manufacturing tasks involving non-cellular components as needed.
- Maintain accurate compliant experimental records in accordance with Good Documentation Practice.
- Draft study protocols and reports with guidance.
- BS degree with 5+ years of laboratory experience or MS with 2 years.
- Hands‑on experience with aseptic cell culture techniques in a BSC.
- Solid understanding of cell biology and cell-based assays.
- Strong attention to detail and organizational skills.
- Ability to work independently and collaboratively within a team.
- Self‑motivated and proactive in learning new skills.
- Excellent written and verbal communication skills.
- Ability to analyze experimental data and summarize findings clearly.
- Flexibility to work variable hours as needed.
- Prior experience working in a GMP-regulated environment is desirable.
- Knowledge and hands‑on experience in drug product development.
- Knowledge and experience of CMC (Chemistry Manufacturing and Control) development.
- Familiarity with GMP standards, ICH guidelines, and global compendial regulations including USP, JP, and EP.
- Prior experience with flow cytometry and plate‑based assays.
- Prior experience with cryopreservation and controlled‑rate freezing protocols.
- Prior experience with cryogenic temperature handling of biological products is desirable.
- Knowledge of Quality by Design, or drafting of risk assessments and FMEA is desirable.
- Familiarity with data analysis and visualization tools such as Graph Pad Prism and JMP.
- Flexibility to work on weekends as needed.
Position Requirements
10+ Years
work experience
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