Pharmaceutical QA/QC Senior Specialist
Company Description
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 and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description
This role will provide Quality Assurance oversight for Quality Control activities, including review and approval of method validations, equipment qualifications, protocols, reports, procedures, and deviations. The role supports implementation of process improvements. This is on-site in Sanford, NC
- Conduct QA reviews and approvals for validation documents, method transfer protocols, change controls, CAPAs, compendial assessments, and related records
- Review deviations, investigations (OOS/OOT/OOE), and other Quality Events/Lab Events, Electronic build of Master Batch or any electronic record when needed, and all associated to compendial changes
- Make real-time quality decisions per regulations, collaborate cross-functionally to resolve technical issues, and support start-up activities as assigned
Qualifications
- Bachelor's or Master's Degree in relatable field (Microbiology, Chemistry, Pharmaceuticals, etc.)
- Bachelor's degree and 6-8 years of experience
- Master's degree and 4-6 years of experience
- Relevant experience includes:
- Manufacturing, laboratory, quality, technical or engineering experience within biotech of the pharmaceutical industry
- Experience in a Quality Control Laboratory and cGMP Laboratory environment.
- Familiarization with Pharmacopeia requirements. (e.g., USP, JP, EMEA amongst others.
- Familiarization with the Data Integrity requirements.
- Deviations, Change Controls, Stability Protocols, and all the implementation activities. Support in CAPA closures, Effectiveness checks, and experience in Root Cause Analysis tools.
- Experience in a quality assurance role, preferably in Quality Assurance for a Quality Control role in the document such as: (e.g., OOS (Out of Specification), OOE (Out of Expectation), OOT (Out of Trend) investigation, specification, method transfer protocol, stability protocol, and others).
- Proven ability to work in a team environment through conflict resolution and negotiation.
- Valid drivers license and personal transportation
- Authorization to work in the United States indefinitely without restrictions or sponsorship.
- Relevant experience includes:
Additional Information
Positions are full-time, Monday - Friday 8am - 5 pm with overtime as needed. Candidates currently living within a commutable distance of Sanford, NC 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.
Average salary estimate
If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.
Eurofins Food Chemistry Madison seeks an entry-level Associate Analytical Chemist to perform routine food chemistry analyses, support QC documentation, and grow technical skills on HPLC/UPLC/GC/LCMS in an ISO 17025 lab.
Eurofins is hiring an Associate Chemist to perform HRMS-based environmental sample prep and analysis on the 2nd shift at its Lancaster, PA laboratory.
Assurant is hiring an on-site NPI/Tool Validation Specialist in Irving, TX to lead product introductions and validate tools and integrations for high-volume consumer electronics manufacturing.
Flock Safety is hiring a Device QA Engineer II to own manual testing and help build a scalable QA framework for Android-based safety devices and companion apps.
Clinical Lab Scientist II needed at Holy Family Medical Center to perform and validate moderate-to-high complexity lab testing, maintain QC, and support accurate patient reporting on a part-time day schedule.
Lead the clinical QA strategy for ABA at Brellium, using clinical expertise and AI-driven insights to improve documentation, compliance, and operational quality across provider networks.
Experienced Mobile Tester needed to perform manual and automated testing (Appium/Espresso) for iOS and Android apps at a Texas City-based IT services company.
Lead the QA environment engineering function for a U.S.-based partner, managing multiple non-production environments, driving QA standards, and mentoring engineers to ensure reliable testing and deployments.
Lead and scale QA strategy for Super.com's BPO network, owning calibration, insights, and vendor alignment to improve agent performance and customer experience.
Solventum seeks a Quality Engineer in Irvine to support medical device quality systems, investigations, and product compliance initiatives.
AbbVie is hiring a Senior Scientist, Quality Control for an onsite, one-year contract to perform GMP analytical testing and support product/material release in Barceloneta, Puerto Rico.
Gain hands-on continuous improvement experience at Cornerstone Building Brands as a CI Intern supporting process improvement projects, documentation, training, and KPI tracking.
Experienced EHS Engineer needed to lead regulatory compliance, audits, incident investigations and sustainability initiatives at a tier-one automotive manufacturing facility.
Experienced food safety leader needed to direct corporate food safety programs and regulatory compliance for a rapidly growing employee-owned supermarket chain headquartered in Boise.
Lead and scale the quality function at an early-stage medical device company, establishing QMS, design controls, risk management, and supplier quality to support Class III product development and first-in-human trials.
🔮
Hi, I'm Risa! Your AI Career Copilot
you, just ask me below!
