QC Analytical Scientist
Eurofins Scientific
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- Location
- Sanford, NC
- Work style
- On-site
- Job type
- Full time
- Posted
- Oct 13
- 7 days ago
Career path
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About the company
Eurofins Scientific
Biotechnology · 10,001+ employees
What you'll do
- Perform analytical testing of pharmaceutical products, raw materials, and samples; operate and maintain laboratory instruments and evaluate data for accuracy and compliance.
- Create, review, and approve GMP documentation, support investigations, and maintain laboratory compliance.
What you need
- Requires a BS in Chemistry or Biochemistry and at least 2 years of laboratory experience.
- Education: a bachelor's degree
Key skills
HPLCUPLCUV-VISGood Manufacturing Practicesanalytical testinglaboratory instrumentsEmpower 3LIMSanalytical standardsAccurate pipetting skillscomplex data analysisStrong organizational skills
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Perks
- comprehensive medical coverage
- dental
- vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
See full description on company page, apply now
Read the full posting here
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:
BS in Chemistry or Biochemistry with a minimum of 2 years of experience working in a laboratory environment, QC laboratory preferred.
Experience working with analytical standards, reagents, and laboratory instruments
Successful hands-on analytical testing experience in a Good Manufacturing Practices {also cGMP} environment
Understanding and performing analytical testing and the use of analytical equipment: i.e. UV-VIS, HPLC, UPLC, pH, appearance, osmolality, TOC and conductivity
Capability to perform complex mathematical problems and perform complex data analysis
Accurate pipetting skills
Strong organizational skills and ability to multi-task across projects and activities
Must be self-motivated and work with minimal direction
Must be authorized to work in the United States indefinitely without restrictions or sponsorship
Preferred Experience:
Empower 3, LIMS
Demonstrate proficiency in computerized systems, such as Laboratory Information Management System
This position is Full-Time, Wed-Sat 7 am - 5 pm . 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.