Job Properties
  • Job Type
    Full-time Position
  • Category
    Security & Surveillance
  • Languages
    English
  • Experience Required
    Entry
  • Degree Required
    Bachelor
    • Province
      Haarlem
    • Date Posted
      September 01,2022
    • All-round Interview Preparation cover
    • Entrusting Package
    • JSS
    • VISA
    • MOCKINTERVIEW
    • IMG_6430
    • Career Consultation

    Group Leader QC- Support, Planning and Coordination

    Who are we?

    Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

    Purpose of the job

    The Group Leader QC- Support, Planning and Coordination will be leading an enthusiastic knowledgeable team consisting out of a team of analysts (±10 prs). The team is responsible for all supportive tasks within the department, ranging from planning, equipment management, LIMS, Inventory management, preparation of GMP administration, sampling of raw materials to arranging shipments. The Group Leader is responsible to plan the various activities in close collaboration with all stakeholders, while remaining aligned with the strategy, commitments and goals of the QC organization. You will act as a department representative in communication with the facility and maintenance departments and will be an expert in keeping overview of all ongoing activities in the team.

    Responsibilities

    • Manage commissioning, decommissioning and data integrity compliance of equipment
    • Guide team in planning, communication and decision making
    • Manage the team in establishing and maintaining quality at the lab in accordance with Site SOP’s, regulatory guidelines and cGXP compliance requirements.
    • Maintain a culture of enhancing quality throughout the entire Laboratory. Performance of in-depth root cause analyses and problem solving
    • Act as a Subject Matter Expert during regulatory and internal audits.
    • Is a Subject Matter Expert with respect to equipment lifecycle management and data integrity.
    • Responsible for cross-departmental communication with stakeholders like Operations and Facilities
    • Manage own team through talent identification, active performance management, succession planning, employee development, mentoring and modeling behavior according to Teva values.
    • Run an efficient and effective QC Planning & Coordination team through managing the team budget and resources.
    • Manage and maintain a culture of enhancing safety throughout the entire Laboratory.
    • Review and provide options to meet business needs without compromising health & safety.

    Qualifications

    • Bachelor or Master degree in analytical chemistry/pharmacy/metrology or equivalent experience
    • Solid experience with equipment used for routine chemical analytical testing
    • Good knowledge of ICH guidelines on data integrity and equipment lifecycle management
    • Excellent organizational skills and a strong affinity with planning and coordination of complex, multi stakeholder activities.
    • Experience with working in a pharmaceutical environment using LIMS and inventory management
    • Management Experience is preferred (2-3 yrs)
    • Good knowledge of pharmaceutical quality systems and production processes
    • Some experience in Lean/Opex
    • Good scientific analytical attitude
    • Excellent written and verbal communication skills - Dutch & English
    • Pro-active team player
    • Results oriented

    Function

    Quality

    Sub Function

    Quality Assurance Methods

    Reports To

    Head of QC Analytical Laboratory

    Already Working @TEVA?

    If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

    The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

    Teva’s Equal Employment Opportunity Commitment

    Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.

     
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