QC Analytical - Group Leader

Eurofins USA PSS Insourcing Solutions•Sanford, NC

4d•Onsite

About The Position

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. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. 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. 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

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