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QC Analytical Scientist
Career Insights for Quality Control Analyst
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Based on North Carolina data
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What they do
A Quality Control Analyst, in the biotech and medical device industries, works in laboratories performing biological, microbiological, and chemical tests on products and materials. Responsible for calibrating equipment, inspecting products, processing and testing materials, and reporting results. May work in other production environments to monitor and improve quality and efficiency in production systems and products.
$73,058 / year median in North Carolina
-11% projected decline
Job Description
- 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.
EUR 6.72
billion, and has been among the best performing stocks in Europe over the past 20 years.- Job Description
- This role performs routine and non-routine analytical testing of pharmaceutical products, raw materials, validation, stability, and process samples within a GMP-regulated laboratory.
- + Independently manage testing priorities, operate and maintain analytical instrumentation, evaluate data for accuracy and compliance, and ensure complete and accurate documentation + Collaborate closely with Quality Operations and may interact with manufacturing, engineering, environmental health and safety, technical services, research teams, and external laboratories as needed + Responsibilities also include supporting investigations, corrective actions, inventory management, material ordering, and maintaining laboratory compliance while delivering reliable, high-quality analytical results that support site operations + Utilize laboratory instruments and equipment in accordance with established procedures to include but not limited to appearance hoods, pH meters, conductivity meters, Solo VPE, Osmometers, UV-VIS, HPLC, UPLC, TOC and conductivity, and various other instruments + Responsible for appropriate creation, review and approval of GMP documentation (test records, and as assigned validation protocols/reports, test methods, equipment records, etc.
- The site is not accessible by public transportation options
Minimum Qualifications:
Preferred Experience:
- + Empower 3, LIMS + Demonstrate proficiency in computerized systems, such as Laboratory Information Management System Must be authorized to work in the United States indefinitely without restrictions or sponsorship.
- Additional Information
- Position is full-time,
- Monday-Friday, generally 8 a.m. - 5 p.m
- ., weekend work might be expected. Candidates currently living within a commutable distance of
- Sanford, NC
- 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 USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.