Teva Jobs

Production Supervisor - Fri-Sun, every other Thurs 6:00 am to 6:30 pm - SLC East

Date: Apr 5, 2024

Location:

Salt Lake City, United States, Utah, 84108

Company: Teva Pharmaceuticals

Job Id: 54064

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity

This position is responsible for providing direct supervision to operators, performing operational administrative in support of the manufacturing or 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.

How you’ll spend your day

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 the daily performance management, providing feedback and identifying and guiding development of direct reports.

• Responsible for managing and executing on staffing needs.

• Maintain a strong shop floor presence – adhere to 70-80% time on the shop floor

• Responsible for completing assigned CAPA’s (Corrective Action/Preventative Action) and performing training of others associated with the assigned CAPA.

• 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/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 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 (cGMP’s), Standard Operating Procedures (SOP’s) and Batch Record instructions.

• Responsible for enforcing safe work practices and company standards

• Perform additional related duties as assigned.

Your experience and qualifications

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

Education/Certification/Experience:

• Bachelor’s Degree required, ideally in a scientific discipline or equivalent education and minimum 3yrs experience.

• Prefer experience in a related industry such as pharmaceutical, nutraceutical, medical device or food processing.

• Prefer experience with cGMP and other applicable industry regulatory requirements as they relate to the production of pharmaceutical products and associated quality systems.

• Strongly prefer previous supervisory or other leadership experience

Skills/Knowledge/Abilities:

• Computer proficiency with comprehensive working knowledge of MS Office products, Learning Management Systems (LMS), ERP systems such as SAP or Oracle and manufacturing/quality systems such as Trackwise, Studium and Qdocs.

• Ability to motivate, influence and lead others with and/or without direct supervisory authority.

• Ability to positively manage conflict, provide difficult feedback and negotiate resolution.

• Ability to build and maintain collaborative relationships between teams, departments and business units.

• Ability to demonstrate sound judgment and decision making.

• Communicate effectively with excellent written and oral communication skills.

• Self-directed with ability to organize and prioritize work.

Problem Solving:

• Works on problems of moderate scope where analysis of situation or data requires knowledge and evaluation of identifiable factors.

• Exercises judgment within broadly defined practices and policies and selects methods and techniques for obtaining solutions.

• Normally receives little instruction on routine work and receives general instructions on new assignments.

• May proactively recommend methods and procedures for problem resolution.

Enjoy a more rewarding choice

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, 13 paid Holidays, 6% match on the 401(k), Employee Stock Purchase Plan, and Tuition Assistance.

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 (https://performancemanager.successfactors.eu/sf/careers/jobsearch?bplte_company=1080030P)

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.

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.

Important notice to Employment Agencies - Please Read Carefully

Teva Pharmaceuticals USA does not accept unsolicited assistance from agencies for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

EOE including disability/veteran