• Jt338 - Specialist Quality Control

    Quality Consulting Group (Juncos, PR)


    QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

    Responsibilities:

    + Functions as the technical specialist for testing & development in areas of molecular biology and microbiology.

    + Focus is on the complex technical issues and scope is typically multi-organizational and/or multi-site and /or involving outside resources.

    + Responsible for providing technical guidance, provide reports, data analysis and ensure flow of communication between technical groups including following up on and resolving issues that arise.

    + Resolve technical issues and troubleshoot for assays as necessary, ensure lab compliance which includes implementing procedures that enhance GMP, GLP and safety.

    + Manage existing and/or develop and implement new programs, processes and methodologies,

    + Develop, revise and audit various complex controlled documents that may have multi-organizational and/or multi-site impact.

    + Approve lab investigations, Lead audit teams

    + Represents the department/organization on various teams, independently responsible for following through on multi-site action items.

    + Performs special projects as requested by supervisor, May supervise employees as necessary to meet technical requirements.

    Qualifications:

    + Bachelors degree background in Chemistry, Microbiology, Biology or Life Sciences

    + 5 years of directly related experience

    +  Laboratory experience in a GMP environment within the Pharmaceutical and/or Biotech industry

    + Fully bilingual communications skills (English and Spanish)

    + Good communications and presentation skills in English and Spanish

    + Project management skills

    + Knowledge of and experience with processes involved in manufacturing and distribution, QA, QAL, validation and process development

    + Basic Knowledge and skills of word processing, presentations, and spreadsheet applications

    + Administrative Shift and 1st shift

     

    Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

     

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