Teva Pharmaceuticals · 4 hours ago
Sr Mgr Quality Assurance
Davie, FL
Full-time
Onsite
Senior Level, Lead/Staff
8+ years expTeva Pharmaceuticals is a leading innovative biopharmaceutical company dedicated to addressing patients’ needs. The Sr Mgr Quality Assurance position is responsible for overseeing the operational aspects of the Quality Assurance Department, managing quality systems, and ensuring compliance with regulations while collaborating with cross-functional teams.
BiopharmaHealth CareMedicalPharmaceutical
Responsibilities
Manages Quality Operations – Quality Systems team activities for EDMS, Investigations, CAPAs, Effectiveness Checks, Protocols, Reports for Equipment Qualifications, Process and Method Validations and the Change Controls associated
Work closely with QC and Production for LIMS, MES, SAP changes
Work closely with Project Managers, R&D, Regulatory Affairs, Quality Control, Quality, Operations and Supply Chain teams for documents review and approval in a coordinated effort, and alignment on site priorities and launch objectives to ensure a seamless and successful KPIs
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 completing all training requirements and maintaining 100% compliance with all assignments
Reviews and approves production and process control Standard Operating Procedures (SOPs) that are drafted, reviewed and approved by other organizational units
Support the identification, investigation, closeout of deviations and Corrective Actions & Preventive Actions
Coordinates with Operations to ensure compliance with and understanding of CGMPs, Company policies and practices, and safety procedures
Support inspections and audits to ensure compliance with CGMPs, SOPs, Company practices and procedures and governmental regulations
Prepare the monthly and quarterly Quality Council report for Deviations, CAPAs, CC, and any other Quality System required
Prepares reports for the Director of Quality and executive management
Provides support, in the areas of disciplinary action, problem resolution and planning
Ensures project deadlines and performance standards are established and met
Responsible for performing additional related duties as assigned
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), and Standard Operating Procedures (SOP’s) instructions
Responsible for performing additional related duties as assigned
Qualification
Required
Requires Bachelor Degree in Science, Engineering, Master Degree preferable from an accredited college or university, with a minimum of 8 years relevant progressive experience in the pharmaceutical industry, including 5 years in supervisor or managerial capacity
Strong Project Management and organizational skills
Analyzing and troubleshooting problems, identifying solutions, recommending and implementing methods, procedures and or/techniques for resolutions
Strong Root Cause Analysis knowledge/techniques on: FMEA, Cause and Effect Diagrams, Fishbone, 5M, 5Why
Responding to technical inquiries from management, peers, and regulatory agencies
Communicating clearly and concisely, both, orally and in writing
Operating scientific and personal computers
Managing multiple projects, duties, and assignments
Interpreting and applying Federal, state, and local policies, procedures and regulations
Directing, coordinating assignments of the QA department personnel
Establishing and maintaining cooperative working relationships with others
Principles of quality assurance management, leadership, and training
Principles of safety, worker's compensation, OSHA, and related principles and practices
Pharmaceutical principles, practices, and their application
FDA, SOP, cGMP and other pertinent regulatory compliance and requirements
Pertinent Federal and State laws related to personnel administration
Skill levels in MS Office including proficiency in Word, PowerPoint, Excel and SharePoint
Must be able to maintain the highest levels of confidentiality, integrity and discretion
Excellent verbal, written, and interpersonal skills required
Preferred
Preferably in a pharmaceutical manufacturing environment or related field
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