Quality Assurance Senior Associate

Aequor Technologies LLC

  • Holly Springs, NC
  • 12 days ago

    Highlights

    Associate Plant Quality Assurance (PQA) on-the-floor position will work directly with plant manufacturing and support groups for on-going bulk drug substance manufacturing and new product introduction-including development, clinical, and commercial operations. Responsibilities: " Provide on-going Quality oversight to ensure products are manufactured, tested, stored, and distributed according to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP) and other applicable regulations.

    Numbers & Facts

    LocationHolly Springs, NC
    IndustryStaffing/Employment Agencies
    Company Size100 to 499 employees

    Description

    Note:
    The role will be sourced at open market rate***
    Fully Onsite, Shift Work Schedule (includes weekends, and possibly nights)
    Shift will be determined once identified, once shift is determined shifts will be on a stable schedule.
    Must have: Manufacturing and PQA background
    Let s do this. Let s change the world. The *** North Carolina (ANC) Sr. Associate Plant Quality Assurance (PQA) on-the-floor position will work directly with plant manufacturing and support groups for on-going bulk drug substance manufacturing and new product introduction-including development, clinical, and commercial operations. The Sr Associate PQA position will facilitate real-time decision making to ensure adherence to GMP quality requirements. This is a unique opportunity to maintain and further build a strong partnership and learning environment between Manufacturing and Quality staff providing coaching, guidance and direction for manufacturing events, deviations, quality systems and compliance

    Responsibilities:
    " Provide on-going Quality oversight to ensure products are manufactured, tested, stored, and distributed according to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP) and other applicable regulations.
    " Ensure that facilities, equipment, materials, organization, processes, and procedures comply with applicable regulations and *** requirements relating to Good Manufacturing Practices, Good Documentation Practices, Safety, and other controls.
    " Drive closure/completion (including review and approve) of cGMP processes, procedures, documents and records, including but not limited to deviations, investigations, corrective action/preventative actions (CAPA)s.
    " Ensure production and testing records/results are complete, accurate, and documented according to procedures, GDP and cGMP requirements.
    " Oversee and provide guidance during on-the-floor analytical testing.
    " Ensure that changes that could potentially impact product quality are assessed according to procedures.
    " Ensure that deviations from established procedures are investigated and documented per procedures.
    " Alert senior management of quality, compliance, supply and safety risks.
    " Provide project management support, leading efforts to drive timely achievement of tasks and develop strategies for system implementation.
    " Identification and implementation of continuous improvement opportunities within our processes and systems.
    " Support and represent PQA during audits and inspections; may directly interact with regulatory agencies during on-site inspections.

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