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Teva API TPO (third party operation) MS&T

Date: Nov 17, 2021

Location: Tel Aviv, IL, 1111

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

 

Purpose of SRT (Service Relationship Team):

Ensure API supply to Teva in high quality, robust process, service standards and competitive cost

 

Purpose of the Teva API TPO MS&T:

Be active member in the team (SRT), provide technological, scientific and EHS support for Teva API supplier, be Teva API process and product owner, support process optimization to improve safety, quality, delivery and cost.

 

Organization:

Part of the Teva API TPO SRT (Service Relationship Team) report direct to SRM (Service Relationship Manager) and proficiently to Teva API head of MS&T

 

Accountability:

  • Support products allocation process from products evaluation, technical package preparation, questionnaires, RFI (request for information) and RFP (request for proposal), supplier proposal evaluation and selection
  • Responsible for the transfers of allocated Teva API products to 3rd party manufacturer (CMO) and be the professional owner of the process and products
  • Demonstrate Teva process to the CMO and support the technology transfer & validation on site
  • Responsible for the validation of products to ensure commercial production while complying with all rules and regulations, evaluate suppliers gaps / risks analysis and mitigation plan
  • Ensures the optimization of products and processes to improve safety, quality, delivery and cost and leading the change management process
  • Supports CMO continuous improvement using OPEX tools to maintain cost competitive product
  • Support supplier qualification process and ensure the implementation of Teva guidelines, standards and SOPs
  • Support supplier to resolve any ad-hoc issue and minimize supply disruption, maintaining high performance and be part of the S&OP, BRM (Business review meeting) and SR (strategic review) routines
  • Support supplier improvement plan based on supplier diagnostic and gaps analysis
  • Collaborates with Global MS&T, Quality, RA, EHS, Procurement, Operations, Supply Chain, Engineering and Commercial

Qualifications

  • University education in the field of Engineering, Chemistry or other related fields
  • More than 10 years of experience in the pharmaceutical industry
  • Expert knowledge of production processes and technologies
  • Basic knowledge of OPEX principles
  • Basic knowledge of RA regulations and other related standards
  • Advanced knowledge of English
  • Customer orientation
  • Willing to travel up to 25%

Function

Manufacturing

Sub Function

Technical Transfer

Reports To

Sr Dir Third Party Ops Regional Head, Mgmt. & Admin.

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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.