Eurofins
Scientist Group Leader
Devens, MA, United States · Full-time
Sponsorship not specified$84k-$94kDetected 1 day ago
Clinical TrialsPharmacologyGMPFDA RegulatoryBioinformaticsResearchMass SpectrometryLeadership
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Entry-level history0
PERM / green-card track0
Lottery odds (Level II)66
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About the role
- 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.
Responsibilities
- Perform release and stability testing on starting materials, intermediates and API forboth development and GMP samples.
- Author and review technical documents including method qualification/validation/transfer protocols and reports for analytical procedures.
- Maintain and troubleshoot analytical instrumentation.
- It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations.
- It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
- The Scientist Group Leader is responsible for the development and implementation of analytical procedures and specifications in support of the development and manufacture of active pharmaceutical ingredients (APIs) for traditional synthetic molecules (including potent) and peptides.
Requirements
- Experience with common analytical techniques such as: HPLC/UPLC, GC, NMR, UV, KF, FTIR, XRPD, LC-MS, GC-MS and ICP-MS.
- Minimum of 5 years' experience in method development and validation for small molecules Active Pharmaceutical Ingredients (APIs).
- Experience with Process Development of APIs.
Nice to have
- Previous leadership experience preferred
Compensation
- $84,000-94,000
Benefits
- Lead the design, development, and execution of phase-appropriate analytical methods in compliance with ICH and Health Authority guidelines.
- Excellent full time benefits including comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- Paid vacation and holidays
Company info
- Responsible for contributing to audit readiness and for participating in quality audits with FDA, other Regulatory Agencies, and customers, as needed.
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This listing is sourced directly from Eurofins's careers page and normalized into a canonical job model.