QC Scientist – Raw Materials & Pharmacopoeia Testing

Eurofins USA PSS Insourcing Solutions

QC Scientist – Raw Materials & Pharmacopoeia Testing

Gaithersburg, MD
Full Time
Paid
  • Responsibilities

    Job Description

    Eurofins PSS is seeking a QC Scientist – Raw Materials & Pharmacopoeia Testing to support the launch and operation of a new GMP raw materials testing laboratory. This role will focus on performing analytical and compendial testing of pharmaceutical raw materials in accordance with USP/NF, European Pharmacopoeia (Ph. Eur.), and Japanese Pharmacopoeia (JP) requirements.

    The ideal candidate will have hands-on experience with raw materials testing, pharmacopoeial methods, wet chemistry techniques, and instrumental analysis, including HPLC, UPLC, GC, and FTIR. This individual will play a key role in maintaining data integrity, supporting laboratory investigations, and contributing to the successful implementation of new methods and processes in a start-up laboratory environment.

    Training will be conducted in both Gaithersburg, MD, and Frederick, MD.

    Responsibilities

    • Perform raw materials testing in accordance with GMP requirements, approved procedures, and applicable pharmacopoeial monographs and general chapters
    • Execute compendial and physicochemical testing, including appearance, identification, pH, and wet chemistry analyses
    • Perform chromatographic and spectroscopic testing using HPLC, UPLC, GC, and FTIR instrumentation
    • Interpret and evaluate analytical results against established specifications and acceptance criteria
    • Document laboratory activities in accordance with ALCOA+ principles using laboratory notebooks, electronic systems, logbooks, and worksheets
    • Troubleshooting laboratory instruments and performed routine equipment maintenance activities
    • Support laboratory investigations, including deviations, invalid assays, OOS/OOT events, CAPAs, and change controls
    • Author and revise SOPs, test methods, protocols, and associated GMP documentation
    • Conduct data review, logbook review, and documentation review activities
    • Support implementation, transfer, and continuous improvement of compendial and analytical methods
    • Maintain laboratory organization and efficiency through Lean and continuous improvement initiatives
    • Assist with inventory management, reagent preparation, sample receipt, storage, and disposal activities
    • Collaborate effectively with cross-functional teams while managing multiple priorities in a fast-paced environment
  • Qualifications

    Qualifications

    Minimum Qualifications

    • Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline
    • Minimum 3 years of pharmaceutical Quality Control laboratory experience
    • Hands-on experience performing pharmaceutical raw materials testing
    • Experience executing pharmacopoeial and compendial methods according to USP/NF, Ph. Eur., and/or JP requirements
    • Experience with physiochemical testing, wet chemistry techniques, and raw materials release testing
    • Proficiency with HPLC, UPLC, GC, and FTIR instrumentation
    • Minimum 2 years of GMP laboratory experience
    • Strong technical writing, documentation, and data review skills
    • Proficiency with Microsoft Outlook, Excel, and Word
    • Authorization to work in the United States without current or future sponsorship

    Preferred Qualifications

    • Experience supporting start-up laboratories or implementing new testing programs
    • Strong understanding of data integrity principles and ALCOA+ requirements
    • Familiarity with Lean, 5S, or continuous improvement methodologies
    • Excellent troubleshooting and problem-solving skills
    • Strong organizational and time-management abilities
    • Ability to work independently while contributing effectively within a team environment
    • Experience authoring investigations, CAPAs, change controls, and GMP documentation

    Additional Information

    Position is Full Time, Monday-Friday, 8am-5 pm. Candidates currently living within a commutable distance of Gaithersburg, MD, are encouraged to apply

    _ Excellent full-time benefits include:_

    • Comprehensive medical coverage, dental, and vision options
    • Life and disability insurance
    • 401(k) with company match
    • Paid vacation and holiday
    • Yearly goal-based bonus & eligibility for merit-based increases
    • Base Compensation: $31-$40 per hour based on education and experience

    Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

  • Compensation
    $31-$31