Job Summary
The Quality Scientist performs analytical testing and reviews laboratory data to support the release, in-process monitoring, and stability assessment of drug substances under cGMP. The role also contributes to operational excellence by leading process improvement efforts, carrying out complex assays, and building technical capability across the team.
Responsibilities
- Conduct analytical testing and review results for cGMP drug substance release, in-process, and stability programs.
- Perform complex assays and help ensure testing activities and data meet applicable quality requirements.
- Lead initiatives to improve laboratory processes and ways of working.
- Provide technical guidance and training to fellow team members.
Qualifications
- Bachelor’s degree in analytical chemistry or a related area, with at least 10 years of relevant experience, or a Master’s degree with at least 5 years of experience.
- Strong understanding of cGMP requirements.
- Experience working in the pharmaceutical or biopharmaceutical industry.
The businesses of Merck KGaA, Darmstadt, Germany provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
