Eurofins

Global lab testing and analytics network

QC Analytical - Group Leader

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours

Full-timeSanford, NC, USA

About the Job

Requirements

A Bachelor of Science degree in Chemistry or Biochemistry and at least 2 years of experience working in a laboratory environment; quality control laboratory experience is preferred.
Experience working with analytical standards, reagents, and laboratory instruments.
Hands-on analytical testing experience in a Good Manufacturing Practices environment.
Understanding of analytical testing and use of analytical equipment, including ultraviolet-visible spectroscopy, high-performance liquid chromatography, ultra-performance liquid chromatography, pH measurement, appearance testing, osmolality, total organic carbon, and conductivity.
Ability to perform complex mathematical problems and complex data analysis.
Accurate pipetting skills.
Authorization to work in the United States indefinitely without restrictions.

Responsibilities

Perform routine and non-routine analytical testing of pharmaceutical products, raw materials, validation, stability, and process samples in a Good Manufacturing Practices-regulated laboratory.
Use laboratory instruments and equipment according to established procedures, including appearance hoods, pH meters, conductivity meters, Solo VPE, osmometer, ultraviolet-visible spectroscopy, high-performance liquid chromatography, ultra-performance liquid chromatography, and total organic carbon instruments.
Create, review, and approve Good Manufacturing Practices documentation, including test records and assigned validation protocols and reports, test methods, and equipment records.
Act as a technical resource, trainer, and troubleshooter for the department.
Recommend operational and technical improvements.
Communicate within the group.
Coach and develop direct reports.
Plan and monitor workflows.
Monitor and approve employees’ time worked through the time-entry system.
Support and promote company policies and procedures.
Work Monday through Friday, generally from 8 a.m. to 5 p.m.; weekend work may be expected.

Desired Qualifications

Quality control laboratory experience is preferred.
Previous leadership experience is preferred.

Job Description

Lab Responsibilities:

Perform routine and non-routine analytical testing of pharmaceutical products, raw materials, validation, stability, and process samples within a GMP-regulated laboratory
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.)

Leadership Responsibilities:

Act as a technical resource, trainer, and troubleshooter for the department
Make recommendations for operational and/or technical improvements
Communicate effectively within the group
Coach and develop direct reports
Plan and monitor workflows
Monitor and approve employees’ time worked through time-entry system
Support and promote company policies and procedures

The site is not accessible by public transportation routes/options.

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
Previous leadership experience preferred
Authorization to work in the United States indefinitely without restrictions

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.

About the Company

Eurofins

Global lab testing and analytics network

Eurofins provides global laboratory testing and analytical services to verify the safety, authenticity, and quality of products across food, water, medicine, and the environment. It operates a network of more than 900 laboratories in over 60 countries, offering access to more than 200,000 analytical methods. Its product work involves running specialized tests—using chemistry, biology, and other scientific techniques—to confirm origin, composition, and compliance of samples, such as detecting wine fraud or contaminant presence. The company differentiates itself through its massive, distributed lab network and broad portfolio, enabling standardized testing at scale and fast turnaround across many industries, rather than relying on a single specialty or location. Its goal is to protect public health and safety by delivering accurate, comprehensive testing data and helping clients meet regulatory and quality requirements.

Company size: 10,001+
Company stage: IPO
Headquarters: Luxembourg
Founded: 1987

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