Eurofins Lancaster Laboratories

Scientist Group Leader

Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • BS in Analytical Chemistry or equivalent with 5+ years experience in analytical development in the pharmaceutical industry.
  • MS in Analytical Chemistry or equivalent with 3+ years experience in analytical development in the pharmaceutical industry.
  • PhD in Analytical Chemistry or equivalent with relevant experience in analytical development in the pharmaceutical industry.
  • Proficiency in techniques like HPLC/UPLC, GC, NMR, UV, KF, FTIR, XRPD, LC-MS, GC-MS, and ICP-MS.
  • Minimum 5 years experience in method development and validation for small molecules APIs, along with Process Development experience.

Responsibilities

  • Lead the design and execution of analytical methods in compliance with regulatory guidelines.
  • Conduct release and stability testing on a variety of pharmaceutical materials.
  • Author and review technical documentation for analytical methods and processes.
  • Maintain and troubleshoot analytical instrumentation to ensure operational efficiency.
  • Contribute to audit readiness and participate in regulatory audits as required.
  • Ensure compliance with state and federal regulations, including GMP and FDA standards.

Benefits

  • Comprehensive medical coverage including dental and vision options.
  • Life and disability insurance for employee security.
  • 401(k) plan with company matching to aid financial planning.
  • Generous paid vacation and holiday offers for work-life balance.
Full Job Description
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. Primary analytical techniques include chromatography (HPLC/UPLC, GC, and IC), Spectroscopy (LC-MS, GC-MS, NMR, ICP-MS, FTIR and UV-Vis), and physical properties (particle size, water content, etc.). Core Responsibilities: • Lead the design, development, and execution of phase-appropriate analytical methods in compliance with ICH and Health Authority guidelines. • 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. • Responsible for contributing to audit readiness and for participating in quality audits with FDA, other Regulatory Agencies, and customers, as needed. • Ensures work in compliance with all state and federal regulations, including but not limited to GMP, DEA, FDA, etc. Qualifications • BS in Analytical chemistry or equivalent with 5+ years related experience in analytical development (R&D and method qualification/validation) environment within pharmaceutical industry. • MS in Analytical chemistry or equivalent with 3+ years related experience in analytical development (R&D and method qualification/validation) environment within pharmaceutical industry. • PhD in Analytical chemistry or equivalent with related experience in analytical development (R&D and method qualification/validation) environment within pharmaceutical industry. • 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. • Previous leadership experience preferred Additional Information The position is full-time, Monday-Friday, 8:00am-5:00pm, with overtime as needed. Candidates living within a commutable range of Devens, MA are encouraged to apply. • Compensation: $84,000-94,000 • Excellent full time benefits including comprehensive medical coverage, dental, and vision options • Life and disability insurance • 401(k) with company match • Paid vacation and holidays

About Eurofins Lancaster Laboratories

Eurofins Lancaster Laboratories is a leading contract research organization (CRO) providing analytical, research and testing services to clients in the pharmaceutical, biopharmaceutical, biotechnology, crop protection, chemical, food, environmental and consumer products industries. The company was founded in 1961 and has grown to become one of the largest CROs in the world, with over 50 locations in 20 countries. Eurofins Lancaster Laboratories is part of the Eurofins Scientific Group, a global leader in bioanalytical testing and laboratory services. The company's services include method development and validation, stability testing, quality control testing, and regulatory compliance support.
Learn more about Eurofins Lancaster Laboratories
Size
12,000 employees
Industry

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