QA and QC Specialist
Summary
QA/QC Specialist at Eurofins' Sanford, NC lab site: provides QA oversight of QC activities — reviewing and approving method validations, equipment qualifications, protocols, and procedures, and supporting deviation investigations. Requires GMP experience and hands-on assay work (HPLC, GC, raw materials testing) in pharma/biotech.
- Responsible for providing Quality Assurance (QA) oversight of Quality Control (QC) activities
- QA review and approval of QC method validation, equipment qualification, protocols, reports, process control documents, and both new and existing procedures
- Support the evaluation and resolution of QC deviations and investigations, and contribute to the implementation of process improvement initiatives
The site is not accesible by public transportation routes.
- BS or BA degree Scientist or related field with a minimum of 4 years of experience in manufacturing, laboratory, quality, technical or engineering experience within biotech or the pharmaceutical industry
- GMP Experience required
- Direct experience needed with: Method Transfer Validation, Investigation, Authoring Change Controls, Equipment Qualification
- Experience with testing and execution of assays such as HPLC, GC, raw materials testing
- Ability to understand and drive process improvements
- Pharmacopia experience preferred
- Authorization to work in the United States indefinitely without restriction
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. This site is not accessible by public transportation options; daily, reliable transportation is needed to and from the site.
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 USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.