QA Specialist - United Kingdom - Allergan

    Allergan
    Default job background
    Description

    Company Description

    AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . Follow @abbvie on Twitter , Facebook , Instagram , YouTube and LinkedIn .

    Job Description

    QA Specialist

    • Based in either the Marlow or Maidenhead offices with flexible working (3/2 model)
    • Reporting to the QA Manager
    • Highly competitive salary, Bonus and comprehensive benefits package.

    Role Objectives

    The Commercial Quality Specialist is responsible for independently providing Commercial Quality support in the affiliate. Scope of activities includes quality system requirements associated with: pharmaceutical products, medical devices, combination products, biologics and cosmetics. Specific areas of support may include Storage and Distribution, potential quality events/product shortage execution, Supplier Controls, Product Quality Review, Risk Management, Agency inspections/internal audits, CAPA, and overall Quality Manual requirements. This position will ensure that all product, process or system related quality activities supporting the business at the affiliate from receipt of final product through distribution are in compliance with Corporate, governmental, and local regulations and requirements.

    Key responsibilities:

    • Responsible for the integration of local quality regulations for drugs, biologics, device and/or combination products and cosmetics.
    • Design effective quality systems, procedures and/or processes within cross functional teams to ensure compliance as well as efficiency throughout our quality systems.
    • Work on assessments to determine compliance to processes, procedures and regulations to identify potential gaps and mitigate and implement improvements.
    • Plan, prepare, review and approve quality documentation such as change controls, product reviews and other local requirements.
    • Support self inspections, internal, external and MoH audits as directed by the manager.
    • Coordinate and investigate quality events such as deviations, non conformances and corresponding action plans including decisions.
    • Execute supplier qualification program including performance monitoring for key suppliers.
    • Monitor metrics and KPIs to ensure compliance.
    • Support all activities governed by Good Storage and Distribution Practices including monitoring of controlled temperature and cold chain shipments.

    Qualifications

    Qualifications:

    • Bachelor's Degree in Chemistry, Pharmacy, Biology, Microbiology, Engineering, other technical/scientific area or equivalent professional experience.
    • Experience in quality assurance, GMP or GDP environment preferred.
    • Strong computer skills, familiarity with SAP, TrackWise, ComplianceWire and OneVault.
    • Full understanding of local GxP requirements including regulations and standards affecting device, biologics, pharmaceutical products and cosmetics.
    • General knowledge and understanding of AbbVie MD, pharmaceutical, biologic and cosmetic products and regulations.
    • Ability to support projects as a team member as assigned by manager.
    • Experience working in both a team setting and independently. Works well with manager guidance to complete tactical objectives while able to manage own time effectively.

    Additional Information

    AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie's policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

    #J-18808-Ljbffr