GMP Chemist - Reference Standards

2w2 weeks ago

Eurofins

Foster City, US · Full-time · $55,000 – $65,000

About this role

Eurofins Scientific is an international life sciences company providing a unique range of analytical testing services to make life and our environment safer, healthier, and more sustainable. In this role, you will support and aid the qualification and requalification of Reference Standards by performing GMP analytical testing.

Day-to-day activities include conducting tests such as Appearance, FTIR, NMR, LC, TGA, DSC, and KF titrations. You will also coordinate shipment and testing plans to external contract labs and upload results into internal databases.

As part of a GMP regulated environment, you will maintain compliance by completing training, SOPs, and other documentation. The role involves performing verification of lab work prior to sample testing to minimize lab investigations and participating in weekly lab cleanups.

Eurofins Lancaster Laboratories Professional Scientific Services® places scientists at client sites to run and manage laboratory services. This insourcing solution leverages over 55 years of scientific and laboratory operations expertise, offering a dynamic environment to develop your skills within a global organization.

Requirements

Demonstrated success in GMP regulated analytical environments
Previous experience conducting and analyzing data for analytical methods such as UPLC/HPLC, Appearance, FTIR, NMR, LC, TGA, DSC, KF titrations
Strong understanding of experimentation and data analysis using Empower software
Ability to communicate complex scientific findings and recommendations in one-on-one discussions and departmental meetings
Demonstrated ability to work as an independent, self-motivated, detail-oriented, result-driven and highly flexible team-player in a fast-paced working environment
Strong computer, scientific, and organizational skills
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
Authorization to work in the United States indefinitely without restriction or sponsorship

Responsibilities

Support and aid qualification and requalification of Reference Standards through GMP analytical testing including Appearance, FTIR, NMR, LC, TGA, DSC, KF, and calculating Correction Factors
Coordinate shipment and testing plans to external Contract Labs and upload results into internal database
Maintain GMP compliance by completing training, SOPs, and other compliance documentation
Perform verification of lab work prior to sample testing to minimize lab investigations
Support lab cleanliness by participating in weekly lab cleanups
Assist in the development and validation of analytical methods for reference standards
Participate in the preparation of certificates of analysis for reference standards