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MS&T Specialist III- SLC East

Date: Jun 15, 2022

Location: Salt Lake City, Utah, US, 84108

Company: Teva Pharmaceuticals

Who are we?

If you’re like people at Teva, you dare to be different. We’re 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.

Teva’s Salt Lake City, Utah production site (s) are two of our complex manufacturing and supply chain operations. Our East site is located at our facility in Research Park, near the University of Utah (Address: 577 Chipeta Way, Salt Lake City, Utah. 84108) & our West Site is located near Salt Lake City International Airport (Address: 4745 Wiley Post Way, Salt Lake City, Utah. 84116).

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 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 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

This position is responsible to support technology transfer, scale-up, process validation and commercialization of pharmaceutical solid dosage forms. This position will provide formulation and process related technical support to groups such as Production, QA, QC and third party personnel for the company’s semi-solid and transdermal products. This position will be responsible for resolving complex technical issues and ensuring that activities meet critical project deadlines and product launch dates.


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 included in other related duties or assignments.

• Responsible for providing hands-on expertise in the areas of mixing, filling, coating, assembly and cartoning.

• Responsible for providing knowledge and experience in the areas of formulation and process development, scale up, validation and optimization for a variety of dosage forms.

• Responsible for leading technology transfer of assigned new projects and technologies to the site from internal and third-party manufacturing sites.

• Responsible for providing technical support in the investigation of manufacturing incidents and deviations and performing investigations as needed.

• Responsible for generating, reviewing and approving technical documentation in support of product lifecycle management per regulatory requirements.

• Analyzes data to ascertain if it meets related protocol acceptance criteria; writes deviation reports as required upon failures to meet protocol acceptance criteria.

• Interfaces with Quality Assurance and Research & Development (R&D) on process requirements for new and current products.

• 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.


• Requires BS degree or equivalent in Pharmacy, Engineering or related discipline.

• Requires 3 - 5 years relevant progressive experience in process and technical services or related experience in technical or scientific roles.

• Project management experience; ability to manage multiple projects, duties, and assignments.

• Intermediate skills in Microsoft Office Suites (Word, Excel, Access, PowerPoint, MS Project)

• Intermediate statistical analysis, computations, and test methodology experience; Knowledge of JMP or MINI TAB preferred.

• Knowledge of or ability to learn current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), OSHA, FDA, EPA, AQMD and other applicable regulatory and safety compliance guidelines.

Teva Pharmaceuticals USA requires all U.S. new hires to be fully vaccinated for COVID-19 prior to the first date of employment. As required by applicable law, however, Teva will consider requests for reasonable accommodations.



Sub Function

Technical Transfer

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’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. 

Nearest Major Market: Salt Lake City