QA Supplier Management Associate

Company Description

The work we do at Eurofins matters, and so do our employees. At Eurofins, 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!  

Job Description

POSITION SUMMARY:

This position will support the Quality Assurance department by performing QA activities related to supplier quality management associated with clinical, commercial, and contract product manufacturing. Key responsibilities include reviewing documentation packages for qualifying raw materials and components as well as service providers and completing raw material enrollment activities. Executes and resolves material quality issues through Supplier Corrective Action Report (SCAR) Program with vendor, maintains compliance for site activities associated with local and global Supplier Management, and maintain compliance with regulatory and Pfizer quality standards.

POSITION RESPONSIBILITIES:

• Review of site documentation including but not limited to, risk and technical assessments, vendor related documentation, material qualification packages, and audit reports associated with clinical and commercial processing and ensuring adherence to regulatory agency requirements, standards, policies and values in timely manner.
• Collaborates and independently engages with a wide range of co-workers, customers and management within the OpU to gather the input and background knowledge needed to complete assignments
• Proactively identifies, takes remedial action, and/or seeks advice when an individual, project, or team goal, deliverable is off schedule
• Anticipates issues and elevates them to appropriate management attention immediately.

Qualifications

BASIC MINIMUM QUALIFICATIONS:

• High School or Associate’s degree with 5-7 years relevant experience or Bachelor’s degree with 2-4 years relevant experience or Master’s degree with 1-2 years relevant experience
• Proficient in Microsoft Office software (Word, Excel, PowerPoint) · Experience in pharmaceutical, medical device, or combination product industry

PREFERRED QUALIFICATIONS:

• ASQ or Certified Quality Auditor a plus

Additional Information

Position is Full Time, Monday-Friday, 8:00am-5:00pm. Candidates currently living within a commutable distance of  Sanford, NC are encouraged to apply. Excellent full-time benefits including comprehensive medical coverage, dental, and vision options.

• 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
• Eligibility for potential yearly Bonus & Merit-Based Pay Increases

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