Job Responsibilities
1. Apply GMP/GLP standards across all responsibilities.
2. Maintain the highest quality standards in all tasks.
3. Demonstrate and promote the company vision.
4. Ensure regular attendance and punctuality.
5. Exhibit strong client service skills, teamwork, and collaboration.
6. Plan proactively and multitask to maximize productivity.
7. Meet quality and productivity metrics, fostering teamwork.
8. Contribute to continuous quality and process improvements within the QA department and laboratories.
9. Understand QAU operations and functions.
10. Perform investigation writing, root cause analysis, and CAPA.
11. Conduct internal audits and walk-through inspections.
12. Review procedures, methods, and protocols.
13. Release analytical reports.
14. Host client audits and respond to findings and recommendations.
15. Provide information for monthly/quarterly quality reports to management.
16. Perform all activities safely and efficiently.
17. Communicate effectively with clients and staff.
18. Diagnose problems, solve simple issues, and suggest solutions for complex problems.
19. Review client or agency documents, identify requirements, and assist with implementing changes.
20. Stay updated on regulatory and industry QA requirements, consulting with clients or authorities as needed.
21. Assist in preparing and delivering regulatory training programs.
22. Mentor specialists to complete assignments successfully.
23. Identify and implement process improvements to enhance quality and productivity while ensuring compliance.
24. Utilize computer skills for accessing information, preparing documents, and other job functions.
Qualifications
1. Experience in investigation writing, root cause analysis, and technical documentation.
2. Ability to track action items and ensure completion.
3. Identify trends in recurring issues.
4. Collaborate with laboratory and support groups to improve quality metrics and implement CAPA.
5. Support internal audits and review/write QAU procedures.
6. Preferred background in Microbiology.
7. Bachelor's degree in Biology, Microbiology, or a related science field.
8. Strong computer skills, including Word, Excel, PowerPoint, and databases.
9. Experience in a GMP environment is preferred.
Company Description
Eurofins Scientific is an international life sciences company providing a range of analytical testing services across multiple industries. It is a leader in food, environment, and pharmaceutical testing, as well as genomics, forensics, and clinical diagnostics. With over 30 years of growth, Eurofins operates more than 800 laboratories in over 50 countries, offering over 200,000 analytical methods to ensure safety and quality of products.
Additional Information
This is a full-time position, Monday-Friday, 2nd shift, with additional hours as needed. Candidates living within a commutable distance of Lancaster, PA are encouraged to apply.
We offer comprehensive benefits including medical, dental, vision, life and disability insurance, 401(k) matching, paid vacation and holidays.
#LI-EB1 Eurofins USA BioPharma Services is an Equal Opportunity Employer, including Disabled and Veteran applicants.
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