What are the responsibilities and job description for the Associate Quality Assurance Scientist position at Eurofins?
Company Description
Eurofins is the world leader in the bio/pharmaceutical testing market. With over €5.3 billion in annual revenues and 55,000 employees across 900 sites in 50 countries, Eurofins is a leading international group of laboratories providing an unparalleled range of testing and support services to the pharmaceutical, biopharmaceutical, food, environmental, and consumer products industries and to governments.
The Eurofins BioPharma Product Testing (BPT) Group is the largest network of harmonized bio/pharmaceutical GMP product testing laboratories worldwide. Eurofins BPT provides comprehensive CMC laboratory services for the world’s largest pharmaceutical and biopharmaceutical companies. The service portfolio supports all stages of the drug development process and all functional areas of bio/pharmaceutical manufacturing, including method development, microbiology, process validation and quality control.
Job Description
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 bachelor's 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 non-routine 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:
- Bachelor's 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
Additional Information
The position is full-time, Monday-Friday, 8am-4pm, with overtime as needed. Candidates within a commutable distance of Lancaster, PA are encouraged to apply.
- Excellent full time benefits including comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
Salary : $5
