Quality Control Information Specialist
Eurofins Scientific
Company Description
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!
Job Description
The primary focus of this position is in support, administration, and configuration of laboratory information system software for the quality control laboratories.
What you’ll do:
As a QC Information Systems (QCIS) Specialist, you will act as an administrator of a variety of GMP computerized systems and business analyst between labs groups and IT including Enterprise projects such as Empower, Biovia Laboratory Execution Systems (LES), Labware LIMS, and other digital initiatives. Candidates should have a technical understanding of Information and Enterprise systems. Responsible for day-to-day job functions, administration, validation and data integrity tasks and can independently represent the team for site and global initiatives.
- Perform day-to-day activities and application administration of lab and manufacturing quality control computerized systems, including maintaining static data.
- Support QC lab functions, providing solutions to a variety of technical problems.
- Participate in software/computer system validation, IT for software/computer applications and fulfill all networking and security requirements, for enterprise software applications.
- Executes protocols, reports, investigations using, and other records, using Veeva on behalf of QC.
- Support QC information system lifecycle management activities from concept, development, validation, implementation, maintenance, to retirement.
Qualifications
Basic Minimum Qualifications:
- Bachelor’s Degree preferably in Information Systems/Technology, Biotechnology, or a related field.
Preferred Qualifications:
- At least a few months experience in information management experience is preferred
- Experience in a scientific lab setting a plus.
Additional Information
Position is full-time Monday-Friday, 8am-5pm with overtime as needed. Candidates currently living within a commutable distance of Frederick, MD 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 USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
