Research Associate

United States, Massachusetts, Westborough Jul 16, 2026 Position Title: Research Associate Work Location: Westborough, MA 01581 Assignment Duration: 3 months Position Summary We 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 & Context The 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. Qualifications & Experience 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 GraphPad Prism and JMP. Flexibility to work on weekends as needed. #J-18808-Ljbffr Spectraforce Technologies