Method Validation & Transfer Associate

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

If you’re looking for a rewarding career, a place to call home, apply with us today!

Position Responsibilities:

• Plan and execute laboratory experiments independently, analyzing data to provide conclusive insights.
• Perform assays in GMP laboratory settings, including chemical, biological, or microbiological testing.
• Collaborate with internal and external teams to support method validation and transfer processes.
• Assist in completing assays for validation and transfer of methods, engaging with the method development team for in-process and final product sample analyses.
• Author and critically review technical reports, adhering to cGMP and data integrity principles.
• Evaluate new instrumentation and analytical techniques as required.

Basic Minimum Qualifications:

• BS+1 year of industry experience, preferably in GMP environment
• Hands-on experience and strong background in either Chemistry, Microbiology or molecular biology assays.
• Experience with troubleshooting assays and improving method performance.
• Strong technical writing and presentation skills.

Preferred Qualifications:

• Experience with method validation and method transfer skills to manufacturing site.
• Experience with bio-process downstream development.
• Resource is expected to be self-motivated and driven and able to manage day to day work activities with minimum direction.
• Should have a positive and teamwork mindset.
• Should be an analytical thinker and use their skills to troubleshoot the daily challenges faced at the workbenches, in data reviewing and documentation.

Position is Full Time, Monday-Friday, 8am-5pm with overtime as needed. Candidates currently living within a commutable distance of Sanford, NC are encouraged to apply.

What we offer:

• 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
• Yearly goal-based bonus & eligibility for merit-based increases

Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.