Parexel International Corp logo

Scientist II or III - Stability Sample Management - FSP

Parexel International Corp
  • PA
    4 days ago

    Job Description

    When our values align, there's no limit to what we can achieve.

    At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

    Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

    We are looking to fill a Scientist 2 or 3 - Stability Sample Management position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in West Point, PA. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This role does not offer sponsorship.

    Qualifications - B.S./M.S. in Chemistry or related discipline and relevant years of experience as listed below

    • Scientist 2 - B.S. with 1-2 years of experience; M.S. with 0-1 years

    • Scientist 3 - B.S. with 3-5 years of experience; M.S. with 1-2 years

    Overview: The Scientist is responsible for supporting stability sample management activities in a GMP-regulated environment, including stability study support, sample handling, documentation, and regulatory compliance for late-stage pharmaceutical development programs.

    Responsibilities:

    • Candidates must routinely lift, carry, and place filled sample bins, shipping containers, and cold-chain coolers (e.g., bins loaded with sample bottles)

    • Coordinate set up of new stability studies

    • Perform routine sample pulls from stability chambers according to established procedures

    • Prepare and label samples for stability studies

    • Prepare samples for shipments to multiple testing laboratories, and process samples for destruction

    • Perform second scientist review of analytical data and GMP documents

    • Notify management of non-conforming events related to the tasks

    • Ensure completion of applicable GMP training prior to performing tasks

    • Ensure compliance with all regulatory requirements (cGMP) and internal policies and procedures

    • Maintain accurate records (e.g., sample chain of custody)

    • Maintain up-to-date training in cGMPs

    • Maintain up-to-date knowledge of USP, Ph.Eur, and ICH Guidances

    Required Skills and Experience

    • Hands-on experience in a pharmaceutical cGMP environment supporting stability sample management and stability chamber operations

    • Experience in a fast-paced, dynamic GMP-regulated environment

    • Experience with LIMS and electronic laboratory notebook

    • Strong customer service orientation with the ability to effectively support multiple cross-functional stakeholders

    • Ability to troubleshoot application issues and identify timely resolutions

    • Strong written and verbal communication skills

    • Excellent attention to detail

    • Proficiency with MS Office applications, including Word, Excel, and PowerPoint

    • Self-motivated with demonstrated efficiency, adaptability, and a positive attitude

    About Parexel

    Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies.

    For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement.

    Come join us!

    #LI-DK1

    EEO Disclaimer

    Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

    Numbers & Facts

    LocationPA
    IndustryAll
    Company Size10,000 employees or more
    Year Founded1982
    Websitehttp://www.parexel.com

    About Company

    The expertise and passion for excellence shared by our people around the world unites us in our mission and drives our success. As a premier service provider to the global biopharmaceutical industry, we give you the opportunity to work with industry-leading clients in an exciting, collaborative environment where career choices and development paths are abundant, and projects are challenging. In fact, PAREXEL works with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. With over 30 years of experience, we have supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market.

    We offer our employees the ability to make a difference globally, while we support them locally in environments full of challenge, collaboration, flexibility and industry-leading growth potential.

    Discover a career at PAREXEL, where exciting challenges and opportunities await you.

    Skills

    • Analysis Skillsunmatched
    • Biologyunmatched
    • Biotech and Pharmaceuticalunmatched
    • Chain of Custodyunmatched
    • Chemistryunmatched
    • Clinical Practices/Protocolsunmatched
    • Communication Skillsunmatched
    • Consultingunmatched
    • Cross-Functionalunmatched
    • Current Good Manufacturing Practice (cGMP)unmatched
    • Customer Support/Serviceunmatched
    • Detail Orientedunmatched
    • Documentationunmatched
    • Drug Developmentunmatched
    • GMP (Good Manufacturing Practices)unmatched
    • ICH Regulationsunmatched
    • Maintain Complianceunmatched
    • Microsoft Excelunmatched
    • Microsoft Officeunmatched
    • Microsoft PowerPointunmatched
    • Microsoft Wordunmatched
    • Presentation/Verbal Skillsunmatched
    • Record Keepingunmatched
    • Regulatory Complianceunmatched
    • Regulatory Requirementsunmatched
    • Sample/Specimen Processingunmatched
    • Specimens/Samplesunmatched
    • Staff Requirementsunmatched
    • Technical Supportunmatched
    • Test Labunmatched
    • Writing Skillsunmatched

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