Bioassay Method Development Scientist – GMP & QC Expertise

Eurofins PSS Insourcing Solutions; Malvern (Chester County); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Medical, Dental, Vision

Life Insurance

Disability Insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins Scientific in Malvern, PA is seeking a full-time scientist to perform testing in support of analytical development and manufacturing processes. You will record data meticulously in GMP-compliant notebooks, troubleshoot assays, and report results with clients as needed.

The role requires aseptic technique and experience with various analytical methods in a GMP environment. The position emphasizes collaboration with QC labs, regulatory support for INDs/BLAs, and maintaining strict data

Qualifications

• Bachelor’s degree in chemistry, biology, or a related life sciences field.
• Strong organization, time-management, and communication skills.
• Solid knowledge of cGMP guidelines, GDP (good documentation practices), and aseptic technique.

Responsibilities

• Perform testing to support analytical development, manufacturing process development, and process validations.
• Accurately record data in a timely manner, maintaining detailed records in compliance with GMP, safety, and environmental requirements.
• Troubleshoot experiments, analyze data, interpret results, and report findings in lab notebooks; collaborate with clients to troubleshoot assays.
• Support regulatory filings, including INDs and BLAs.
• Provide technical support (ELISA, FRETS, cell-based assays, flow cytometry, PCR, gel electrophoresis, Western blot) with development and QC labs.
• Handle and maintain cell lines following aseptic techniques in GMP labs.

Skills

Organizational skills

Time management

Communication skills

Education

Bachelor's degree in chemistry, biology, or related life sciences

Job description

Eurofins Scientific in Malvern, PA is seeking a full-time scientist to perform testing in support of analytical development and manufacturing processes. You will record data meticulously in GMP-compliant notebooks, troubleshoot assays, and report results with clients as needed.

The role requires aseptic technique and experience with various analytical methods in a GMP environment. The position emphasizes collaboration with QC labs, regulatory support for INDs/BLAs, and maintaining strict data