30 days old

Production Supervisor (Friday-Sunday, 6am-6:30pm)

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 Pharmaceuticals is looking to fill a Production Supervisor at our Salt Lake City, Utah site. This position is responsible for providing direct supervision to operators, performing operational administrative in support of the packaging of drug products and supporting department management by providing direction to staff and in meeting production schedules in compliance with all regulatory requirements, company policies and procedures.

 

Shift: Friday-Sunday, 6am-6:30pm

 

Job 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 completing assigned CAPAs (Corrective Action/Preventative Action) and performing training of others associated with the assigned CAPA.
 Responsible for the daily performance management and development of direct reports.
 Responsible for ensuring that training documentation is maintained and current to verify that Operators are trained and certified to perform their assigned work activities through Performance Based Training (PBT) and operations are only performed by those with appropriate training.
 Responsible for evaluating work in progress and resolving production, quality, equipment and other issues by working with appropriate departments and making real time decisions in response to unexpected events.
 Responsible for executing assigned continuous improvement initiatives (Operational Excellence).
 Responsible for creating and updating Master Batch Records and SKU Forms.
 Responsible for performing reviews and approvals of completed batch records, test data and inspection forms.
 Responsible for maintaining process equipment system user access.
 Responsible for creating and revising Standard Operating Procedures for supervisor/manager approval.
 Responsible for the resolution of ERP system issues related to packaging.
 Responsible for completing all training requirements and maintain 100% compliance with all assignments.  
 Responsible to maintain work areas and perform 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.
 Perform additional related duties as assigned.

Qualifications

 High School Diploma or equivalent required.
 Preferable Associates Degree, preferably in a scientific discipline or equivalent education/experience.
 Minimum of 2 years relevant experience in a regulated industry required; Pharmaceutical, nutraceutical, medical device or food processing industry experience preferred. 
 Prefer experience with cGMP and other applicable industry regulatory requirements as they relate to the production of pharmaceutical products and associated quality systems.

Function

Manufacturing

Sub Function

Manufacturing/Operations

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: 2021-04-14 Expires: 2021-06-13

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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Production Supervisor (Friday-Sunday, 6am-6:30pm)

Teva Pharmaceuticals

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