Overview
Pharmaceutical QA Senior Specialist – Group Leader Jobs in Sanford, North Carolina, USA at Eurofins QTA Inc.
Pharmaceutical QA Senior Specialist – Group Leader
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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical, and cosmetic product testing, as well as in agroscience Contract Research Organisation services. It is a market leader in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences, and clinical studies support. The company is expanding its presence in Contract Development and Manufacturing Organisations, highly specialized molecular clinical diagnostic testing, and in-vitro diagnostic products.
Over the past 30 years, Eurofins has grown from one laboratory in Nantes, France, to 58,000 staff across a decentralized network of 900 laboratories in over 54 countries. The company offers a portfolio of over 200,000 analytical methods to evaluate safety, identity, composition, authenticity, origin, traceability, and purity of biological substances and products.
This position provides Quality Assurance oversight for Quality Control (QC). Responsibilities include reviewing and approving quality method validation, QC equipment qualification, QC protocols, reports, process control documents, and handling deviations and investigations. Supports process improvements and implementation.
This role is based in Sanford, NC.
Position Responsibilities:
Perform QA technical reviews for validation documents, method transfer protocols, and other related documents.
Provide final QA approval on change controls, effectiveness checks, CAPA implementations, and assessments related to the business unit.
Review and approve documents such as deviations, complaint investigations, laboratory investigations (OOS/OOT/OOE), and other quality events.
Make quality decisions in real-time according to regulations and procedures.
Collaborate with internal partners to resolve technical issues.
Support start-up activities and perform other duties as assigned.
Qualifications:
Bachelor’s or Master’s Degree in Microbiology, Chemistry, Pharmaceuticals, or related field.
Bachelor’s degree with 6-8 years of experience or Master’s degree with 4-6 years of experience.
Experience in manufacturing, laboratory, quality, technical, or engineering roles within biotech or pharmaceutical industries.
Familiarity with cGMP laboratory environments and pharmacopeia requirements (USP, JP, EMEA, etc.).
Knowledge of Data Integrity, deviations, change controls, stability protocols, CAPA, root cause analysis, and quality assurance processes.
Proven ability to work collaboratively, resolve conflicts, and negotiate effectively.
Valid driver’s license and personal transportation.
This is a full-time position, Monday-Friday, 8AM-5PM. Candidates living within a commutable distance to Sanford, NC are encouraged to apply.
Benefits include comprehensive medical, dental, and vision coverage, life and disability insurance, 401(k) with company match, paid vacation and holidays.
Eurofins USA PSS Insourcing Solutions is an Equal Employment Opportunity employer, supporting Disabled and Veteran applicants.
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Title: Pharmaceutical QA Senior Specialist – Group Leader
Company: Eurofins QTA Inc.
Location: Sanford, North Carolina, USA
Category: Quality Assurance – QA/QC
