Eurofins Lancaster Laboratories

Senior QC Analytical Chemist - Group Leader

Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • BS or MS in Chemistry, Pharmaceutical Sciences, Life Sciences, or a related field with appropriate GMP/GLP testing experience
  • Minimum 5 years of GMP experience (BS) or 3 years (MS) in a relevant field
  • 3+ years of industry experience with Liquid Chromatography (LC), Conductivity, and Titration
  • Proficiency in at least two analytical techniques, including NMR, GC, and ICP-OES
  • Strong knowledge of GMPs, ICH guidelines, and 21 CFR regulations
  • 1+ years of prior leadership experience
  • Authorization to work in the U.S. indefinitely without sponsorship

Responsibilities

  • Conduct testing and review per approved methods and specifications
  • Adhere to GMP regulations including 21 CFR Parts 210 and 211
  • Test various pharmaceutical samples such as raw materials and APIs
  • Participate in method transfer and qualification studies
  • Support investigations for out-of-specification and invalid results
  • Utilize a range of analytical techniques like NMR, GC, LC, and TGA
  • Manage reference standard qualification and elemental impurities testing

Benefits

  • Comprehensive medical, dental, and vision coverage
  • Life and disability insurance options
  • 401(k) plan with company match
  • Paid vacation and holidays
  • Eligibility for yearly performance-based bonuses and salary increases
Full Job Description
Job Description

Eurofins PSS is currently hiring for a Senior QC Analytical Chemist Group Leader to support and lead GMP testing of pharmaceutical in-process, raw materials, intermediates, APIs, and stability samples. In addition, the successful candidate will support investigations of invalid results, method transfer activities, and lead a team of 3-5 individual contributors. This individual will have high attention to detail and possess excellent organizational skills.

Key Responsibilities:
  • Conduct testing and review in accordance with approved methods, specifications, protocols, and compendial requirements
  • Follow protocols for GMP regulations, including 21 CFR Parts 210 and 211, and applicable ICH guidelines
  • Testing of pharmaceutical samples including in-process, raw materials, intermediates, API, stability, and more.
  • Participate in method transfer, qualification, and verification studies
  • Support investigations for OOS, OOT, and invalid results
  • Utilize various analytical techniques including: NMR, GC, LC, ICP-OES, IR, RI, UV-Vis, Conductivity, Specific Rotation, Titration, TGA, and more
  • Reference standard qualification and management
  • Elemental impurities and residual solvent testing and review

Leadership & Team Management Responsibilities:
  • Lead, manage, and develop a team of chemists.
  • Serve as a proactive and effective point of contact for client and internal teams.
  • Participate in new hire interviews and onboarding processes as needed
  • Disseminate administrative communications and promote company vision
  • Ensure adherence to highest quality and efficiency standards in laboratory operations
  • Perform administrative tasks to support team member growth and development
  • Balance technical work with team leadership responsibilities
  • Foster morale, collaboration, and teamwork with the group


Qualifications

Basic Minimum Qualifications:
  • BS in Chemistry, Pharmaceutical Sciences, Life Sciences, or related degree with 5+ years of GMP/GLP testing experience; OR MS in Chemistry, Pharmaceutical Sciences, Life Sciences, or related degree with 3+ years of industry GMP/GLP testing experience
  • 3+ years of industry experience with Liquid Chromatography (LC), Conductivity, and Titration
  • Proven experience utilizing at least two of the following techniques and/or instruments:
    • Nuclear Magnetic Resonance (NMR), Gas Chromatography (GC), Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES), Infrared Spectroscopy (IR), Refractive Index (RI), Ultraviolet-Visible (UV-Vis), Thermogravimetric Analysis (TGA)
  • Knowledge and in-depth understanding of GMPs, ICH, and 21 CRF guidelines
  • 1+ years of prior leadership experience
  • Authorization to work in the United States indefinitely without restriction or sponsorship

Preferred Qualifications:
  • At least a year of GMP experience
  • 2+ years of successful leadership experience


Additional Information

This position is a permanent, full-time role with overtime as needed. Candidates currently living within a commutable distance of Albany, NY are encouraged to apply. The position will work 6am-6pm on a rotating schedule - the following shifts are available:
  • Sunday, Monday, Tuesday & every other Wednesday
  • Thursday, Friday, Saturday & ever other Wednesday

Excellent full-time benefits include:
  • Comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
  • Eligibility for yearly goal-based bonus & merit-based increases
  • Compensation: $36.50-$41.00 per hour based on education, past leadership, and related industry experience


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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