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Clinical Supply Chain Manager

Date: Nov 18, 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!

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.

We offer a competitive benefits package including Medical, Dental, Vision, and Prescription coverage starting 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. For more information on Teva, check us out at www.tevapharm.com or www.tevausa.com

Job Description

In this role you will assist in designing, planning and managing of the supply chain for global trials for all clinical phases in partnership with other functions.

 

Essential Job Duties and Responsibilities:
•    Provides input for clinical study team in order to define study timelines, kit design and supply planning
•    Plans the secondary packaging and facilitates the process for final drug release.
•    Initiates label generation and oversees approvals, label regulatory adaptation and translations activities in collaboration with CRO and 3rd party vendors
•    Participate in the IRT (Interactive response technology) system, set-up and oversees maintenance 
•    Maintains the interaction with CROs, CMOs and other vendors to execute the business requirements of the CSC operational systems 
•    Responsible for Accountability, Returns and Destruction of supplies 
•    Responsible for the CMC collection of documents for CTA submission.
•    Responsible for maintaining the CSC TMF documents in TGE
•    Ensures compliance of the clinical supply activities with the ICH GCP, GMP, GDP guidelines and Teva SOPs

Qualifications

What you will bring to the role (minimum requirements)
Do you have a Bachelors Degree from an accredited college or university?
Do you have least 3 years’ experience in pharmaceutical or clinical supply related field? (5 years preferred)
Do you have at least 2 years' experience in GMP and International Council for Harmonization (ICH) guidelines (Annex 13) relative to clinical supply chain activities? (5 preferred)
Do you have at least 1 years' experience in Shipping of Investigational product in both North American and Internationally? (5 preferred)
 

Function

Research & Development

Sub Function

Clinical Supply Logistics

Reports To

Assoc. Dir., Global Gx & Biosimilar Clinical Ops

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. e 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.


Nearest Major Market: Philadelphia