29 days old

Manufacturing Services Associate

West Chester, PA 19380
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

The Manufacturing Associate, Biologics will contribute to the Manufacturing Services group within the brand new state-of-the art Biologics Manufacturing Facility (BMF) located in West Chester, PA. We are seeking a highly self-motivated person willing to contribute to the qualification and operation and overall success of the manufacturing operations.This includes, but is not limited to material weigh/dispense, medium preparation, buffer preparation, and autoclave/washer processes.

May also include cell culture activities including seed expansion, along with production bioreactors (up to 2000 L) and cell culture harvest and/or purification activities including column packing, column chromatography, virus removal steps, tangential flow filtration (TFF) and aseptic filling operations for Tevas proprietary and biosimilar biologics pipeline. In addition you will assist in developing procedures (SOPs/Master Batch Records) for the manufacturing group. You will complete assigned tasks associated with clinical manufacturing and assist in execution of operations as well as performreview of the manufacturing documentation of the associated area.

Other job duties:

  • Assist in troubleshooting equipment or process issues.
  • Initiate and complete deviations, change controls, investigations, as assigned using TrackWise or any similar software system.
  • Compliance to safety guidelines and current Good Manufacturing Practices (cGMP).
  • Ability to train other associates and willing to be involved in cross-training in other groups, as required.
  • Follow standard operating procedures and assist in validation needs such as IOQ and PQ.
  • Ability to multi-task and work well with the team and complete all training documentation within a defined time-frame.
  • Analyze in process samples generated from cell culture or purification activities by using osmometer, pH/conductivity meters, scales, spectrophotometers, Vi-cell, Nova, BGA, etc.
  • Practice a continuous improvement mindset by making suggestions on process improvements.
Qualifications

REQUIRED QUALIFICATIONS:

  • Associates degree in biology, chemistry or a related scientific/technical area or 2+ years of experience within cGMP manufacturing
  • Minimum 2 years ofhands on experience within large molecule and/or clinical manufacturing

PREFERRED QUALIFICATIONS:

  • 5+ years combined experience in cGMP manufacturing
  • B.S. in biology or related life-sciences field
  • Experience with process development, tech transfer and optimization a plus
  • Experience with UNICORN software and cell culture/fermentation a plus
  • Experience with process control SCADA software (e.g., WonderWare)
  • Experience with single use manufacturing systems
  • Experience with medium and buffer solution preparations within a cGMP environment
  • Strong background in aseptic technique and microbial controls
  • Experience with process development, tech transfer and optimization a plus
  • Strong understanding of cGMPs as applicable to biologic operations
  • Ability to work flexible working hours,and have excellent oral and written communication skills
  • Ability to read, interpret, and follow SOPs, batch documents and other procedures
  • Ability to work off-shifts and weekends, as required
Function
Sub Function
Reports To
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.

Categories

Posted: 2020-10-26 Expires: 2020-12-24

Join us at the forefront of pharmaceutical research and production. With state-of-the-art facilities, highly skilled colleagues, and a high-powered organizational culture, Teva offers you countless possibilities to make a real difference in people's lives and add value to your career.

Before you go...

Our free job seeker tools include alerts for new jobs, saving your favorites, optimized job matching, and more! Just enter your email below.

Share this job:

Manufacturing Services Associate

Teva Pharmaceuticals
West Chester, PA 19380

Join us to start saving your Favorite Jobs!

Sign In Create Account
Powered ByCareerCast