Production Supervisor
Teva Pharmaceuticals
Jakarta, ID
2 hari yang lalu
source : DirectEmployers Association

Production Supervisor Date : Jun 24, 2020 Location : Jakarta, ID, 13710 Company : Teva Pharmaceuticals Company Info 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! Job Description To lead one of production area activities starting from planning , preparing, implementing and follow up and projects within prevailing current GMP of Local and European regulations, EHS Policy and corporate policy with the objective toensure that high quality products are produced according to Production Plan and business objective.

  • Lead and supervise the whole process on one of Production area Activities In order to ensure readily availability of high quality product produced in accordance to production plan.
  • Generate and update all technical Standard Operations Procedures, batch manufacturing procedures, validation protocols & reports, all GMP related documentations in order to comply with current GMP, GDP, EHS Policy and company policy (deviation, investigation report).
  • Prepare, conduct and evaluate technical training throughout related production area In order to Ensure all Production team are technically sound and foster EHS Policy and current GMP compliance+ Review validation protocol and report, implement all process and validation works In order to c omply with current GMP, GDP and company policy+ Implement the GMP, GDP and QHSE procedure to achieve the target and continuously improving the effectiveness of the process.
  • Control Departmental Expense, to be fully aware with department budget in all activities in order to meet budget expectation and guidelines.
  • Qualifications + Apothecary Education.+ 1, 2 years experiences in production of pharmaceutical industry.+ Having leadership, presentation and / or training skills.

  • Computer literacy & English. Function Manufacturing Sub Function Manufacturing / Operations Reports To Production Manager 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 SiteThe 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.

    EOE including disability / veteran

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