Eurofins Lancaster Laboratories

Senior Scientist- Raw Materials

Eurofins Lancaster Laboratories • $80K — $110K *
Lancaster, PA 17603In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
6 days ago
Job Overview by Ladders

Qualifications

  • Current authorization to work in the US indefinitely without restriction or sponsorship.
  • Bachelor's degree in chemistry or related concentration, or equivalent experience.
  • Minimum of 4 years in the pharmaceutical industry.
  • Experience with a range of analytical instrumentation and techniques.
  • Familiarity with GMP compliance and documentation procedures.

Responsibilities

  • Perform physical, chemical, and instrumental analysis of pharmaceutical products.
  • Run various chromatographic systems and other instrumental analyses independently.
  • Prepare samples and standards for analytical testing with minimal supervision.
  • Set up and validate new analytical processes within the department.
  • Execute method transfer protocols to maintain quality standards.
  • Document all work meticulously for GMP compliance.
  • Conduct monthly maintenance of laboratory equipment.

Benefits

  • Full-time working schedule with first or second shifts available.
  • Opportunity for some travel (25%) as part of the role.
  • Competitive work environment in a reputable pharmaceutical company.
Full Job Description
  • Perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products (tablets, capsules, parenteral, devices, aerosols, liquids, creams, and gels)
  • Run the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, IR, ICP, AA, TGP, DSC, PDA, auto-titrators, TLC, and dissolution apparatus
  • Preparing samples for analysis and running some instrumentation with minimum supervision
  • Set up and validate new analytical or related processes used by the department
  • Prepare standards and samples for analysis
  • Execute method transfer protocols
  • Document work as required for GMP compliance
  • Perform monthly maintenance of laboratory equipment


Qualifications

Minimum Qualifications:
  • Current authorization to work in the US INDEFINITELY without restriction or sponsorship
  • Bachelor's degree in chemistry or other related degree concentration, or equivalent directly-related experience
  • Minimum of 4 years of pharmaceutical industry experience


Additional Information

Working schedule will be Full-Time Mon-Fri, First Shift 8am-5pm OR Second Shift 3pm-11pm. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. 25% travel may be required. This position is NOT remote.

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
Pharmaceuticals & Biotech
* Ladders Estimates

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