15 days old

Senior Manager, Global Quality Computer Systems

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 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

The primary function of this role will be to provide Quality oversight of certain computerized systems used by Teva.  The incumbent will serve as the global business owner of a key Teva Electronic Document Management System (EDMS).   

 

In addition, this role will be developed to provide Quality oversight and input into Tevas global Serialization projects. Teva has a mature serialization program, and this position will help to ensure that final late-stage aspects of the program are completed (e.g. aggregation). 

 

Key activities include working with the business, IT and other stakeholders to set the strategy and define the business priorities for the EDMS and other system(s) that fall within the scope of the role, while ensuring regulatory commitments and internal Teva requirements are met. The role will also collaborate with stakeholders and internal customers on the development and implementation global harmonization guidance and templates to enhance use of the systems and improve corporate- wide compliance; and directing business related activities such as business process mapping and enhancement review in support of Global Quality computer systems.

 

Duties include: 

  • Serve as the Global Business Owner and Quality representative for EDMS and other Global Quality computer systems as assigned
  • Manage defined implementation of schedules/activities related to program-level project planning and strategy, site implementations, system enhancements, and global roadmap planning
  • Ensure local deployments are aligned with global processes and standards
  • Act as the Global Business Owner for system validation (review/approval of system requirements and other validation documentation). This activity requires knowledge of those deliverables associated with computer system validation.
  • Global Quality oversight and input into remaining product serialization program activities (after training)
  • Provide program status updates in Quality Global/ Segment leadership meetings, as requirement
Qualifications
  • Bachelors in Science is required and advanced degree preferred in science / regulatory / computer science / management field
  • Minimum of 5-7 years in pharmaceutical or related industry is required
  • In-depth knowledge of pharmaceutical quality and quality systems, with broad experience and exposure to best practices Knowledge of cGxP requirements, Quality related IT applications, and computer system validation
  • Demonstrated experience with roadmap planning and managing complex projects. Experience in project and/or program management leading cross-functional teams Experience in a\ regional and/or global role
  • Experience with product serialization preferred but not required
  • Verbal and written communication excellence required
Function
Quality
Sub Function
Quality Compliance
Reports To

Sr Dir, Global Quality Systems Management, Quality Management (US Quality) (US Quality Ops Mgmt)

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: 2020-09-14 Expires: 2020-10-29

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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Senior Manager, Global Quality Computer Systems

Teva Pharmaceuticals

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