Job Summary: Eurofins BioPharma Product Testing (US) is seeking an entry level Quality Assurance Scientist to join their Small Molecular Method Development and Validation team in Lancaster PA. This individual will review data according to cGMP regulatory standards and ensure that clients receive sound quality data. Qualified candidates will have a bachelors degree in a relevant major and a strong attention to detail.
- Determine if data is compliant and defendable based on industry regulations and methodology
- Verify scientific data is of sound quality following all method industry and client requirements where applicable
- Ensure that the client receives quality data by reviewing laboratory data for accuracy clarity and adherence to GMP and/or GLP regulations
- Review simple and complex routine and nonroutine data (for three or more areas) according to departmental corporate and client SOPs; read and understand analytical procedures; ensure all work is performed according to GLP/GMP requirements and apply GLP/GMP in all areas of responsibility as appropriate
- Diagnose problems solve simple problems and suggest solutions to complex problems in professional area
- Review methods to ensure procedures are followed
- Authorize written reports (e.g. SOP OMC client reports)
Qualifications :
Minimum Qualifications:
- Bachelors degree in chemistry biochemistry pharmaceutical science or other related degree concentration
- Authorization to work in the U.S. without restriction or sponsorship
The Ideal Candidate Would Possess:
- Strong attention to detail
- Previous experience with Excel
- Strong written and verbal communication
Remote Work :
No
Employment Type :
Fulltime