Mgr Quality Function

Teva Pharmaceuticals • Magna, UT

3h

About The Position

We Are TevaWe’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.The OpportunityThis position provides direct supervision of the site compliance team to effectively conduct internal audits, supplier qualification, site inspection readiness and knowledge management activities. This position also provides compliance oversight, communication and required documentation to third party and global Teva partners.  How you’ll spend your dayAll 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.

Requirements

• Any equivalent combination of education, training and/or experience that fulfills the requirements of the position will be considered. 
• Bachelor’s Degree, preferably in a scientific or engineering discipline, or equivalent education/experience.
• Minimum 5 years of relevant progressive experience in Quality, Operations or QC Lab including at least 4 years performing audits and measurements of GMP Quality Systems, preferably in the pharmaceutical industry.
• Minimum 3 years of previous supervisory or other relevant leadership experience.
• Requires experience and knowledge of cGMP and other applicable industry regulatory requirements as they relate to the production of pharmaceutical products and associated quality systems.
• Working knowledge of FDA, EMA, DEA, EPA and other regulatory requirements for a research and commercial environment.
• Experience with standard operating procedure development and implementation and inspection management, pre-approval inspections preferred.
• Experience negotiating agreements, terms and conditions.
• Proficient in MS Office, LMS platforms, EDMS/ERP systems, LIMS, and TrackWise.
• Strong leadership skills with the ability to motivate and influence without direct authority.
• Skilled in conflict management, delivering difficult feedback, and negotiating resolutions.
• Able to build and maintain collaborative cross‑functional relationships.
• Demonstrates sound judgment and effective decision‑making.
• Excellent written and verbal communication skills.
• Effective at partnering with colleagues, management, and external stakeholders.
• Strong analytical skills with the ability to develop metrics aligned to business objectives.
• Change‑management capability, including identifying improvement opportunities and guiding teams through transitions.
• Advanced presentation and project management skills.

Nice To Haves

• GMP, ISO or ASQ auditing credentials preferred.

Responsibilities

• Responsible for the daily management and development of direct reports.
• Responsible for collaborating with Site Operations and Quality Management to manage compliance issues and ensure timely resolution while meeting internal and Partner requirements.
• Responsible for facilitating, presenting and communicating status of the overall structure of site quality systems via management review forums, such as Site Quality Council.
• Responsible for managing and executing against internal audit programs to periodically audit procedures, records and systems to ensure compliance with relevant national and international regulatory agencies and guidelines.
• Responsible for providing effective processes and communications to prepare for, manage, and provide follow-up for regulatory and partner inspections/PAI/audits, including timely responses and CAPA commitments tracked to completion.
• Responsible for collaborating with relevant stakeholders to define and maintain a supplier evaluation, qualification and approval system that meets regulatory and commercial operation requirements.
• Responsible for working with partners to manage updates to Quality Technical Agreements (QTA) and communicate details to site management to assure adherence to the individual details of the QTA’s.
• Responsible for maintain appropriate licensing of the site with the regulatory bodies where products are marketed.
• Responsible for supporting the quality unit with review of investigations, corrective action plans, notification to management and field action documentation for compliance requirements and clarity in documentation.
• 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.

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.

What This Job Offers

• Job Type: Full-time
• Career Level: Manager