MS&T Manager (Manufacturing Science&Technology)
Teva Pharmaceuticals
Jakarta, ID
37 menit yang lalu
source : DirectEmployers Association

MS&T Manager (Manufacturing Science&Technology) Date : Jun 26, 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! Role Summary This position is responsible for leading and managing the site MS&T team including the initiation, execution and management of departmental projects (including trial, scale up and validation) to support a consistent supply of quality drug product to the market.

This position will manage cleaning and process validation activities, technology transfer and provide formulation and process related technical support to groups such as Production, QA, QC and third party personnel for the company's all dosage form commercial products.

This position is responsible for ensuring that activities meet critical project deadlines and product launch dates. Key Responsibilities All areas of responsibility listed below are essential to the satisfactory performance of this position by any incumbents with reasonable accommodation if necessary.

Any non-essential functions are assumed included in other related duties or assignments.+ Responsible for the daily management and development of direct and indirect reports.

  • Responsible for providing direction, coordinating project tasks, team responsibilities and timelines and assure results are produced.
  • Responsible for assisting with departmental goal establishment and monitor to effectively accomplish specific team objectives.
  • Other Responsibilities : Not limited to : + Responsible for the design and execution of experiments to optimize and scale-up drug process operations such as blending, compression, granulation and coating of solid dose formulations.

  • Responsible for preparing and / or reviewing documents to support projects such as change controls, protocols, master batch records, investigation reports, SOP's, etc.
  • Responsible for providing technical support for manufacturing investigations, incidents and deviations.+ Responsible for leading and executing projects designed to improve quality and safety, reduce costs and improve efficiency.
  • Responsible for performing additional related duties as assigned. Qualifications + Bachelor Degree in Pharmacy, Apothecary preferably.
  • 3-5 years experiences in technology transfer / product development / quality control in pharmaceutical industry.+ CGMP, GLP, Indonesian Regulation.
  • Analytical skill, Leadership, interpersonal skill.+ Computer literacy & English profiency.+ Requires experience with solid dosage manufacturing with an in-depth understanding of process validation, quality by design, quality assurance, quality system and regulatory requirements for global markets.
  • Requires working knowledge of raw material physical properties and relevance to solid dosage forms, equipment and unit operations associated with blending, milling, granulation, drying, compression and coating.
  • Function MS&T Sub Function MSandT Technical Transfer Reports To Site GM 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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