Vacancy expired!
Job Description
- Collecting details from cross-functional departments to create and update the Production Release Materials Specification documents
- Responsible for material qualification activities
- Perform quality review and approval of Material Safety Risk Questionnaires (MSRQs)
- Submit LIMS build for raw material enrollments
- Review and approve associated material enrollment tasks
- Perform quality approval SAP tasks
- Support supplier change notifications and change controls
- Supplier qualifications (supplier assessment review, audit reviews, supply channel approvals)
- Adhere to site safety standards, participate in routine safety training events, and enforce safety and biosafety requirements as they relate to the Clinical Manufacturing department
- Able to work in a fast-paced environment, task oriented, and a team player
- Strong attention to detail
Qualifications
The Ideal Candidate would possess:- Knowledge of pharmaceutical supply chain or QA experience preferred
- Strong computer skills; specifically, Excel and SAP
- Organization/project management skills
- Able to work both independently and as a member of a cross-functional project team in a fast-paced environment
- Bachelor's degree in a scientific or engineering discipline or similar, with a minimum of 1-2 years GMP experience.
- Authorization to work in the United States indefinitely without restriction or sponsorship
- Valid driver’s license and personal transportation
Additional Information
Position is full-time, Monday - Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance of Sanford, NCand the surrounding areas 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
Eurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
Vacancy expired!