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Quality Analyst I

Date: Jul 12, 2019

Location: Salt Lake City, US, 84116

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!

 

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.  This position is located at our facility in the International Center, near the Salt Lake City International Airport (4745 Wiley Post Way, 84116). For more on Teva, check us out at www.tevapharm.com or www.tevausa.com.

Job Description

 

POSITION SUMMARY

This position is responsible for actively investigating deviations, recommending corrective and preventative actions, and assistance in implementing the identified corrective actions. 

 

ESSENTIAL AREAS OF RESPONSIBILITY

All areas of responsibility listed below are essential to the satisfactory performance of this position by any incumbents with reasonable accommodation if necessary. Any non-essential functions are assumed to be included in other related duties or assignments.

 

  • Responsible for evaluating deviation incidents and working with QA to determine if incidents should be escalated to an event investigation.
  • Responsible for conducting comprehensive investigations of simple and/or straightforward events as assigned.
  • Responsible for completing all actions necessary in system to document investigations, identify root causes, create and assign appropriate CAPA’s and gain approval and closure of an event.
  • Responsible for monitoring CAPA’s for completion and effectiveness as applicable.
  • Responsible for maintaining continuous compliance to cGMP documentation of all investigations as well as completion of CAPA’s on a timely basis leading to sustained regulatory compliance.
  • Responsible for updating open events tracking system for the status of all assigned events.
  • Responsible for updating documents (SOPs, MBRs, forms, etc.) as assigned.
  • Responsible for completing all training requirements and maintaining 100% compliance with all assignments.  
  • Responsible for maintaining work areas and performing job functions in a safe and efficient manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMP’s), Standard Operating Procedures (SOP’s) and Batch Record instructions.
  • Responsible for performing additional related duties as assigned. 
Qualifications

 

POSITION REQUIREMENTS

 

Any equivalent combination of education, training and/or experience that fulfills the requirements of the position will be considered.

Education/Certification/Experience:

  • Requires Bachelor’s Degree in Science or Engineering or equivalent education/experience with a minimum of 2 years relevant experience in pharmaceutical industry.
  • Requires experience with the handling of deviations, investigations and CAPA’s.
  • Requires experience with and an in-depth knowledge of cGMP and other applicable industry regulatory requirements as they relate to the production of pharmaceutical products and associated quality systems.
  • Experience in Solid Dose manufacturing environment preferred.
  • Experience within engineering, production, quality, validation or other relevant functional area preferred.
  • Experience with Manufacturing/Quality systems such as Trackwise, Learning Management Systems, ERP Systems, and statistical software preferred.
     
Function
Quality
Sub Function
Manufacturing Quality Assurance
Reports To
In process of validation
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.


Nearest Major Market: Salt Lake City