20 days old

Operation/Clinical Supplies Project Associate

Salt Lake City, UT 84111
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!

 

We offer a competitive benefits package including Medical, Dental, Vision, and Prescription coveragestarting on the first day.  We also offer Disability and Life Insurance, Paid Time Off, 6% match on the 401(k),Employee Stock Purchase Plan and Tuition Assistance. or more information on Teva, check us out at www.tevapharm.com or www.tevausa.com

 

Primary Responsibilities:

  •  An understanding and application of principles, concepts, practices, and standards in area of clinical supply logistics. Understands the working knowledge of how clinical research fits into overall R&D.
  • Provides answers for complex issues in area of clinical supply aligned with study plans/protocol.  Suggestions are developed that provide solutions to moderately complex problems, which require the regular use of ingenuity and innovation.
  •  With limited supervision exercises independent judgment in developing work processes, techniques and evaluation criteria for obtaining results. Work efforts are reviewed to ensure acceptance by proposed goals.
  • Adjusts to the changing priorities.  Ensures that the ever changing demands have appropriate resource allocation.
  • Acts according to Standard Operating Procedures, Best Practice Guidelines.  Takes direction from leader in the clinical supply logistics arena.

 

Essential Duties & Responsibilities

  • Assist in managing global clinical drug supply activities to ensure available drug supply for ongoing studies: for label coordination, labeling and packaging into corresponding kits, distribution timeline and coordination of product shipment logistics;
  •  Assist with continuous supply of clinical trial material for all ongoing studies for initial shipments and patient resupply activities. 
  • Supports process generation, SOPs, template creation/revision for clinical drug supply activities.
  • Assist with product label and packaging activities. Oversee packaging operators during clinical protocol execution.
  • With minimal supervision Identifies and generates the requests of labels, kits, and boxes.
  •  Ability to multi-task and handle multiple projects at once while balancing timelines and priorities across generics, specialty and biosimilar groups
  • Assist with the management of a variety of logistics issues, including but not limited to inventory control, import-export, shipment of products
  •  Assist with the documentation for the return of drug product and destruction. Identifies issues for the teams, if applicable.

 

 Minimum high school degree or equivalent combination of education, training, & experience.

Experience Required:
 Experience with Distribution and operating in a GMP/highly regulated environment
 Inventory Control Experience
 Ability to work under tight deadline and fast-paced undefined environment
 Ability to work autonomously and/or with a team
 Excellent problem solving, judgment and decision-making skills
 Strong verbal, written and presentation skills
 Superior time management, planning, and organizational skills
 Ability to multitask and effectively prioritize workload
 Experience with: MS Excel, MS Word, MS PowerPoint


Specialized or Technical Knowledge, Licenses, Certifications needed:
 GMP and/or GCP knowledge and working knowledge of the drug development process and clinical trials is preffered.
 Knowledge of IRT systems

Categories

Posted: 2020-05-11 Expires: 2020-06-21

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.

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Operation/Clinical Supplies Project Associate

Teva Pharmaceuticals
Salt Lake City, UT 84111

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