QC Analytical - Group Leader
About The Position
Eurofins Scientific is an international life sciences company providing a unique range of analytical testing services to clients across multiple industries. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. 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 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. 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.
Requirements
- 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
- Authorization to work in the United States indefinitely without restrictions
Nice To Haves
- Previous leadership experience preferred
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.)
- 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
Benefits
- Comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
