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!  

POSITION SUMMARY:

We have an exciting opportunity for a Document Coordinator to help our PSS client set-up a new laboratory. This position will create and revise documents provided by a sister client location.

POSITION RESPONSIBILITIES:

• Performing all aspects of maintaining the document control system and performing word processing duties for procedures
• Perform lab start up activities (method writing, coordination of activities, planning for critical paths)
• General quality duties including authoring and review of change controls, investigations, deviations, and review and release of specifications
• Creation and modification of SOPs, reports, protocols, and training presentations
• Applies GMP/GLP in all areas of responsibility, as appropriate
• Maintain document control records and accurately enter new procedure as needed
• Ensure all files are accurate and precise
• Maintain accurate posting of procedures; archive revised procedures in a timely manner
• Perform word processing of procedures as required and understand and recognize QA requirements for procedure formatting
• Back up Archives
• Conducts all activities in a safe and efficient manner

BASIC MINIMUM QUALIFICATIONS:

• Bachelor’s or Master's degree (preferred) in biological sciences or another scientific discipline
• Lab startup experience is required (method writing, coordination of activities, planning for critical paths) - this will be the critical function of the role. 
• Minimum of 6 years of relevant biopharmaceutical industry experience 
• Minimum of one-year of work experience in a laboratory Quality-based role
• Knowledgeable in the use of different Quality Management software packages and terms (i.e. Pilgrim, Trackwise, Master Control)
• Experience in the creation and modification of SOPs, reports, protocols, and training presentations

Position is Full Time, Monday-Friday, First Shift. Candidates currently living within a commutable distance of Holly Springs, NC 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
• Eligibility for potential yearly Bonus & Merit-Based Pay Increases

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