Sr Mgr, Commercial Quality US

Date:  Jan 29, 2026
Location: 

Parsippany, United States, New Jersey, 07054

Company:  Teva Pharmaceuticals
Job Id:  66105

We Are Teva

We’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 opportunity

The primary purpose of the Senior Manager Commercial Quality is to perform various Quality/Compliance related activities for the Teva USA Quality Systems and Regulatory Compliance Department as well as support all manufacturing sites that provide products to the USA Market.  This includes but is not limited to being responsible for processing and driving to closure the various Notifications to Management Reports, Field Alert Reports, Recalls Drug Shortage Reporting, and process the Corporate Quality Standards to provide assurance that Teva remains compliant with all GMP related Regulations and maintains an excellent quality and compliance reputation in the industry.

 

The position is associated with the lifecycle management of Products at the Teva USA and works together with the partners within Commercial USA, including: 


•    Liaison with the Teva Quality sites located outside of the USA for filing any of the reports with FDA. 
•    Responsible to execute the formal market action decision as dictated by Senior Quality Unit Management and the Market Action Committee and author Product Recall Letter.  Circulate draft Recall Letter to Quality Unit Management for review and compile and resolve suggestions/comments.

•    Work with Regional FDA District Recall Coordinator to coordinate the FDA’s review of the Recall Letter. 
•    Monitor the Notification to Authorities for potential notifications to FDA of any potential Field Alert Reports, Biological Product Deviation Reports, Medical Device Reports, Illegitimate products reporting, Drug Shortage Reporting and Recalls.   

•    Utilize the Enterprise Resource Planning System to identify remaining inventory within Teva Control as well as all customers to whom product was distributed to.
•    Send Recall Letters to all Customers and applicable Business Partners
•    Liaison with Teva’s Contracted Recall Service Provider to ensure proper handling, reconciliation, and destruction of products returned for a recall event.  Ensure Recall Effectiveness Checks are performed.
•    Submit Recall Update Progress information to the FDA monthly
•    Submit information for closure of the Recall to FDA.

•    Perform activities necessary to communicate specific Drug Shortage events and periodic updates to FDA Drug Shortage Staff.  Work with Commercial team on obtaining information for periodic updates to FDA.
•    Provide weekly updates to FDA Drug Shortage Staff (DSS), respond to request for information by FDA DSS and update the FDA DSS Drug Shortage Webpage on a biweekly basis based on information obtained from Supply Chain and Commercial teams. Keep management informed of critical potential supply interruptions that could affect the Company reputation.
•    Prepare and provide weekly Supply Interruption report.  
•    Conduct the applicability and gap assessment for the CORP STDs for the Quality Systems & Regulatory Compliance Dept.  Author new/enhance existing SOPs to close gaps by the Effective Date of the CORP STD. Ensure the GAP assessment is performed within deadlines to ensure updates are completed prior to the Effective date of the CORP STD. 

•    Work with various Quality Systems and Process Owners to ensure North Wales/Parsippany sites are Inspection Ready.
•    Provide support to Inspection related activities including but not limited to: Scribing Notes from Inspection conversations, performing Back Room coordination activities, retrieving/reviewing requested records, daily summary notes, etc.
•    Provide Regulatory Agency Inspection support to Teva sites who supply products to USA market.  
•    Lead and/or support internal audits, including audit scheduling, audit planning, conducting audits, and audit reporting 

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 in a scientific discipline
•    A minimum of 5 years of Quality Compliance Leadership related experience in the Pharmaceutical (or related) industries
•    Functional knowledge concerning Pharmaceutical Quality Assurance, Quality Control and Regulatory Compliance 
•    Excellent GMP knowledge
•    Strong knowledge of Excel; knowledge of Veeva, and/or SAP is a plus
•    Excellent written communication skills
•    Teamwork and negotiation skills
•    Ability to professionally and successfully interact with all levels of management
•    Ability to juggle, correctly prioritize and advance multiple activities and projects simultaneously

Compensation Data

The annual starting salary for this position is between $109,520 – $143,745 annually.  Factors which may affect starting salary within this range and level of role may include geography/market, skills, education, experience and other qualifications of the successful candidate.

How We'll Take Care of You

We offer a competitive benefits package, including: 

  • 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

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 policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.    


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. Request a reasonable accommodation by sending an email to disabilityassistance@tevapharm.com with the nature of your request and your contact information. Only inquiries concerning a request for a reasonable accommodation will be responded to from this email address.   

 

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.