7 days old

Quality Engineer I

Salt Lake City, UT 84111

Company Info

If youre like people at Teva, you dare to be different. Were making well-being a way of life for our customers and our colleagues. Join us in helping to make healthcare more accessible to more patients while supporting one of the most innovative teams in the industry.

 

Tevas Salt Lake City, Utah production site (s) are two of our complex manufacturing and supply chain operations.

 

We are strengthening and adding to our critical teams with great talent and capabilities: Teva, a global organization with a brand of evolving success. Be part of it!


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.

 

Teva is a global pharmaceutical leader and the worlds 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 worlds largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we have 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

Teva is looking to fill a Quality Engineering I role in Salt Lake City, Utah. This position is responsible for providing Quality Assurance support to Manufacturing, Supply Chain and Quality Control Laboratories by providing QA review and approval of new and existing methods/procedures, validation/transfer protocols, investigation documentation, and process/facility change control documents.  This position supports teams using trend and investigational data to create value through process improvements and failure reduction activities, and provides representation for quality department on cross functional teams. 

 

Responsibilities & Duties:

 

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 providing a thorough and timely review and approval of cGMP documents and processes such as those related to validation, change documentation, deviations, investigations, equipment and facilities qualifications, protocols and reports, and facility controls, instruments and procedures.
 Responsible for review and approval of activities in the site change control system.
 Responsible for providing first response and ongoing QA presence for quality and compliance issues on the manufacturing floor and as needed in the laboratories.
 Responsible for compiling and maintaining metrics and tracking logs for sites quality KPIs or other functions.
 Responsible for working with operating departments to facilitate process improvements and lean concepts.
 Responsible for participating in cross functional improvement and process monitoring teams to mitigate unfavorable trends.
 Responsible for assistance with research and development products and related document reviews/approvals including change control items, protocols, batch records and deviations as applicable and product disposition.
 Responsible for supporting activities within electronic systems as needed, such as LIMS, TrackWise, EAM.
 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 (cGMPs), Standard Operating Procedures (SOPs) and Batch Record instructions.
 Responsible for performing additional related duties as assigned.

Qualifications

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

 

 Requires a Bachelors Degree or equivalent in Science or Engineering.
 Requires a minimum of two years of relevant progressive QA experience in the pharmaceutical or a related industry.
 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.
 Requires working knowledge of the handling of deviations, investigations and CAPAs.
 Experience in a solid dose manufacturing environment preferred.
 Experience with Manufacturing/Quality systems such as Trackwise, LIMS/Labware, Crystal Reports, Learning Management Systems and statistical software preferred.
 Experience with laboratory related investigations/inquiries preferred.

Skills

 Detail oriented with ability to analyze information and create corresponding performance metrics.
 Computer proficiency with comprehensive working knowledge of MS Office products and computer relational databases.
 Ability to demonstrate sound judgment and decision making.
 Ability to build and maintain collaborative relationships between teams, departments and business units.
 Communicate effectively with excellent written and oral communication skills.
 Interact positively and collaborate with co-workers, management and external partners.
 Manage conflict and negotiate resolution.
 Self-directed with ability to organize and prioritize work.
 Project management and advanced presentation skills a bonus.

Function

Quality

Sub Function

Manufacturing Quality Assurance

Reports To

In process of validation

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 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.

 

We 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.

Categories

Posted: 2021-04-29 Expires: 2021-05-29

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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Quality Engineer I

Teva Pharmaceuticals
Salt Lake City, UT 84111

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