Teva Pharmaceuticals · 11 hours ago
Quality Analyst I
Salt Lake City, UT
Full-time
Onsite
Entry Level
3+ years expTeva Pharmaceuticals is a leading manufacturer of generic medicines dedicated to making health more affordable. The Quality Analyst I position is responsible for reviewing batch records, supporting production operations, and ensuring compliance with regulatory requirements.
BiopharmaHealth CareMedicalPharmaceutical
Responsibilities
Responsible for conducting review and release activities associated with manufactured product release with some oversight, but minimal and directed at anomalous issues or observations
Responsible for performing activities to support Production Operations which includes floor support, audit/walkthrough support, AQL assessment, investigation assessment, and training
Responsible for compiling and maintaining metrics and tracking logs at the request of management and is responsible for successfully hitting metrics delivery schedules
Responsible for reviewing and approving edits to Master Batch Records submitted for revision and for ensuring accuracy and GMP compliance in documents that are being reviewed
Responsible for supporting investigations and process improvement initiatives in the Quality and Production Areas as well as supporting ongoing quality and compliance initiatives at the site including support of Lean Management initiatives (TLMS) (i.e. reducing events or documentation related to human errors)
Responsible for revising or reviewing Standard Operating Procedures (SOP’s), forms and/or Work Instructions with changes of low complexity and responsible for ensuring accuracy and GMP compliance in documents that are being reviewed
Responsible for completing all training requirements and maintaining 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
Qualification
Required
Requires a Bachelor's degree or equivalent education/experience with a minimum of three years relevant experience in a manufacturing environment within pharmaceutical, medical device, nutraceutical, or food processing industries preferred
Requires working knowledge of cGMP, DEA and other applicable industry regulatory requirements as they relate to the production of pharmaceutical products and associated quality systems
Computer proficiency with comprehensive working knowledge of MS Office products, Learning Management Systems (LMS), ERP system such as SAP or Oracle and manufacturing/quality management systems such as TrackWise, Veeva and Glorya
Self-directed with ability to organize and prioritize work with ability to independently determine prioritization needs and demonstrate flexibility to adjust to changing priorities
Ability to communicate effectively with excellent written and oral communication skills
Ability to interact positively and collaborate with co-workers, management and external partners
Works on problems of moderate scope where evaluation of contributing factors requires analysis of situation or data
Exercises judgment within broadly defined practices and policies and selects methods and techniques for obtaining solutions
Acts independently and proactively to recommend methods and procedures for problem resolution
Preferred
ASQ Certification preferred but not required
Benefits
Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment, providing the employee enrolls.
Retirement Savings: 401(k) with employer match, up to 6% and an annual 3.75% Defined Contribution to the 401k plan.
Time Off: Paid Time Off including vacation, sick/safe time, caretaker time and holidays.
Life and Disability Protection: Company paid Life and Disability insurance.
Additional benefits include, but are not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible , Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more.
Company
Teva Pharmaceuticals
Teva Pharmaceuticals is a pharmaceutical company that develops generic and innovative medicines.
10001+ employees
H1B Sponsorship
Teva Pharmaceuticals has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (7)
2024 (4)
2023 (23)
2022 (48)
2021 (31)
2020 (33)
Funding
Current Stage
Public CompanyTotal Funding
$5.51BKey Investors
Royalty PharmaBerkshire Hathaway
2026-01-11Post Ipo Equity· $500M
2025-05-20Post Ipo Debt· $2.3B
2023-11-13Post Ipo Equity· $100M
Leadership Team
Dipankar Bhattacharjee
President & CEO: Generics Europe
Richard Francis
President and Chief Executive Officer
Recent News
2026-01-17
2026-01-14
2026-01-14
Company data provided by crunchbase