Teva Pharmaceuticals · 6 hours ago
Mgr Quality Control
Forest, VA
Full-time
Onsite
Mid, Senior Level
5+ years expTeva Pharmaceuticals is a leading innovative biopharmaceutical company dedicated to addressing patients’ needs. The Mgr Quality Control position is responsible for coordinating and managing all work associated with the commercial production schedule, overseeing QC testing sections, and conducting laboratory investigations.
HealthcarePharmaceuticalBiopharmaHealth CareMedical
Responsibilities
Responsible for management and development of direct and indirect reports
Responsible for overseeing projects carried out by senior direct reports
Responsible for assisting and coordinating the initial and on-going training of analysts and technicians with regard to safety, regulatory and cGMP issues associated with working in the QC Laboratory
Responsible for prioritizing and coordinating testing of raw material, in-process, bulk product, packaged finished product, stability samples, micro samples, and/or water samples for analysts, as needed to support manufacturing. Assist in the checking/auditing of raw data and various logs generated by analysts
Responsible for liaising between QC functional groups (Finished Product, Raw Materials, Sampling, etc) and internal and external partners to set priorities and schedules to meet timelines
Responsible for generating a rolling daily/weekly Master Planning Schedule for Quality Control Lab based off the priority of Operations
Responsible for compiling QC Metrics (internal and corporate) and communicating within and above site as required
Responsible for conducting or coordinating the creation of Incident, Deviation and Out of Specification Investigation and Out of Trend Investigation reports
Responsible for assisting in maintenance of equipment and computerized systems as needed. This includes overseeing maintenance, qualification and GMP status of laboratory instruments needed for sample analysis or other analytical work
Responsible for performing complex revisions to Standard Operating Procedures, Test Methods, and Specifications
Responsible for coordinating and designing activities associated with the stability program including sample management activities and data analyses and performing statistical analyses
Responsible for project management activities for certain projects related to capacity, efficiency, and utilization
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 (cGMPs), Standard Operating Procedures (SOP’s) and Batch Record instructions
Responsible for performing additional related duties as assigned
Qualification
Required
Bachelor's degree in chemistry or related scientific discipline or equivalent with a minimum of 5 years relevant progressive experience in a Quality Control laboratory environment
Minimum of 2 years of management experience in an environment supporting a production operation
Requires experience with an in-depth knowledge of cGMP and other applicable industry regulatory requirements as they relate to the production of pharmaceutical products and associated quality systems
Requires advanced understanding of the principles of analytical chemistry and/or microbiology as it applies to the responsible area
Advanced abilities related to technical writing and documentation activities. Able to design and document a process with little to no oversight
Advanced understanding of the fundamental principles and theory behind a variety of analytical techniques, including, but not limited to GC, FTIR, NEAR-IR, UV Spectroscopy and TOC
Computer proficiency with comprehensive working knowledge of MS Office products, Learning Management Systems (LMS), ERP systems such as SAP/Oracle and manufacturing/quality systems such as Trackwise/Veeva and Qdocs
Communicate effectively with excellent written and oral communication skills
Self-directed with ability to organize and prioritize work
Ability to identify the developmental needs of others and provide coaching, mentoring or encouragement to help others improve their knowledge or skills
Ability to motivate, influence and lead others with and/or without direct supervisory authority
Ability to positively manage conflict, provide difficult feedback and negotiate resolution
Ability to build and maintain collaborative relationships between teams, departments and business units
Ability to demonstrate sound judgment and decision making
Ability to analyze information and create metrics relevant to the business objectives
Proactively works on problems of a moderate to complex scope where evaluation of contributing factors requires the analysis of situations or data and an in-depth knowledge and evaluation of various known and unknown factors
Seeks out all resources when selecting methods and techniques for obtaining results
Acts independently and proactively to recommend and administer methods and procedures for problem resolution
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.
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
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