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Manufacturing Planning Associate

Date: Nov 20, 2021

Location: West Chester, Pennsylvania, US, 19380

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!
 
R&D:
Teva’s Global Research & Development (R&D) organization is devoted to the development of new medicines, devices and combination products that provide meaningful therapeutic benefit to patients worldwide. Combining creativity, scientific rigor and our extensive knowledge on a broad range of technologies, our scientists, engineers, medical doctors and project leaders across the globe use their expertise to innovate novel biologics, biosimilars, small molecule specialty medicines, generics and over-the-counter therapies
 

Job Description

 

 

The Production Planner will be a key member of the GMP Manufacturing Operations group within the Biologics Manufacturing Facility located in West Chester, PA.  We are seeking an experienced and self-motivated production planner to play a major role in the overall success of operations.

Typical areas of responsibility of Production Planning are coordinating with Project Management, Manufacturing, Purchasing, and Process Development, to maintain inventory of controlled materials in order to ensure materials are available to support the production schedule.

 

Specific Responsibilities:

 

  • Submit and track purchase orders to support existing min/max level inventories and ensure timely delivery to meet manufacturing schedules
  • Perform cGMP and non-cGMP inventory management to support Drug Substance, Cell Bank and Drug Product manufacturing as well as QC operations
  • Managing inventory of controlled materials per established SOP's
  • Perform transactions in electronic inventory system and maintain accurate documentation of inventory
  • Budget management
  • Receipt of cGMP material within the purchasing system and approval of invoices in the electronic inventory management system
  • Vendor management, working with vendors on open orders to expedite critical items
  • Continually interact with floor management and project leads to resolve material needs
  • Support implementation of SAP for the West Chester site as needed

Qualifications

 

What you will bring to the role:

 

Minimum Requirements

 

  • Minimum of a Bachelor's degree and at least 3 years of demonstrated production planning experience to include cGMP receiving, shipping, and inventory of raw materials, consumables, and supplies.  
  • Working knowledge of MS Office
  • Must be able to read, interpret, and follow SOP's, and other procedures
     

Preferred Qualifications

 

  • Three years of production planning experience in the cGMP biopharmaceutical industry
  • Strong understanding of cGMPs as applicable to biologic operations
  • Strong organization and problem-solving skills
  • Good customer service/phone skills and flexibility for handling a wide range of activities
  • SAP systems experience
     

 

Function

Sub Function

Reports To

Sr Dir, Biologics Manufacturing, Biologics CMC

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.

 

We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to  support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Teva Pharmaceuticals USA requires all U.S. new hires to be fully vaccinated for COVID-19 prior to the first date of employment. As required by applicable law, however, Teva will consider requests for reasonable accommodations.

 


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