USA-Validation Specialist III - Swiftwater, United States - TalentBurst

    TalentBurst
    TalentBurst Swiftwater, United States

    1 month ago

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    Description

    Industry:
    Biotechnology



    Title:

    Validation Specialist III

    Job ID:
    SNFIJP



    Location:

    Swiftwater, PA (Hybrid)

    Duration: 12 months (+Possibilities of extension)
    *THIS IS A CLEANING VALIDATION POSITION.


    Duties

    Experience in cleaning validation in the biologics or vaccine industry to include the following:
    o Experience in authoring, reviewing, executing and approving validation documents.
    o Interface with Quality organization and the ability to defend rationale in validation documents.
    o Ability to develop cleaning cycle and lead the investigation or trouble shooting.
    o Ability to review and analyze data.


    Cleaning Validation experience
    o Acceptance criteria determination
    o Sampling plans and sample size determination
    o Rinse and Swab sampling experience
    o Bracketing and worse case rating
    o QC testing requirements
    o Dirty hold times and clean hold times


    Basic Qualifications:


    • Experience utilizing Microsoft Word, Excel, and Outlook
    • Experience writing and revising documents (e.g. testing methods, protocols, reports)
    • Experience performing testing in a GMP setting
    • MS Project experience

    Skills


    • Proficiency in utilizing documentation system to author protocols and reports
    • Experience participating in teams and collaborative work environments.
    • Good communication skills (verbal and written), math skills, general computer skills
    • Team environment a must
    • E Doc/GEODE+ experience with a working knowledge of templates, workflows and approval process
    • Strong root cause analysis with cGMP experience.

    Education


    • BS/MS in Science (e.g. Chemistry, Biochemistry, Analytical Chemistry) or Engineering (Chemical or Biochemical) with 2+ total years of experience working in a biologic, vaccine or pharma industry

    Notes from the Manager:

    Mainly M-F with some flexibility in working hours. Will work some form of 8 hours within 7am and 5pm. Prefer new hire to be open to very occasional weekend work or overtime if needed. May also need to switch a shift from morning to afternoon here and there. Start ASAP with possibility to extend after December 2024.

    Mostly hybrid - will usually be 4 days onsite and one remote but manager prefers flexibility just in case they are needed onsite the extra day.

    Minimum 1-3 years validation experience, open to more experience within rate range. No degree requirements but bonus if related.


    MUST HAVE:
    1. cleaning validation experience 2. strong communication skills 3. ability to manage, execute and troubleshoot on their own 4. Strong Microsoft Suite skills


    PH_EN