Director Of QA jobs in United States
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Medivant Healthcare · 2 months ago

Director Of QA

Medivant Healthcare is a U.S.-based pharmaceutical manufacturer specializing in sterile injectable generic medications. The Director of Quality Assurance will provide strategic leadership for quality systems and regulatory operations, ensuring compliance with FDA and cGMP regulations while fostering a culture of quality across the organization.

ManufacturingPharmaceuticalSales
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H1B Sponsor Likelynote

Responsibilities

Lead and manage the Quality Assurance department, including quality systems, document control, and compliance functions
Serve as the company’s primary quality authority for all cGMP-related matters, including product release and regulatory inspections
Oversee batch review, deviation investigations, CAPA programs, and change controls
Ensure adherence to 21 CFR Parts 210/211, USP <797>/<800>, and other applicable regulations
Lead and support external audits, including FDA, DEA, and State Board of Pharmacy inspections
Collaborate with Manufacturing, QC, Validation, and Regulatory Affairs to maintain compliance throughout the product lifecycle
Review and approve SOPs, validation protocols, and quality-related documentation
Establish and maintain an effective Quality Management System (QMS) and metrics tracking program
Drive initiatives for continuous improvement and risk mitigation across quality processes
Provide leadership, training, and mentorship to QA staff to ensure competency and alignment with Medivant’s standards
Represent the company in regulatory discussions and serve as a key decision-maker for compliance matters

Qualification

Quality AssuranceFDA complianceCGMP knowledgeRegulatory inspectionsAseptic operations experienceSterile injectable experienceMaster's degreeQuality Management certificationAnalytical skillsLIMS familiarityERP familiarityElectronic QMS familiarityLeadershipProblem-solvingCommunication skills

Required

Bachelor's degree in Chemistry, Microbiology, Pharmacy, or related scientific field
Minimum 10+ years of progressive Quality Assurance experience in pharmaceutical manufacturing, with at least 5 years in sterile injectable or aseptic operations
In-depth knowledge of FDA, cGMP, USP, and ICH guidelines
Proven success managing regulatory inspections and quality systems
Demonstrated leadership in building and developing QA teams
Strong analytical, problem-solving, and communication skills

Preferred

Master's degree or higher in a scientific or regulatory discipline
Experience in 503B outsourcing, sterile fill-finish, or parenteral drug production
Familiarity with LIMS, ERP, and electronic QMS platforms
Certification in Quality Management (ASQ-CQA, CQM/OE) or Six Sigma

Benefits

Annual performance-based bonus eligibility.
Comprehensive health, dental, and vision coverage.
401(k) with employer match.
Paid time off, holidays, and professional development programs.

Company

Medivant Healthcare

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Medivant Healthcare is a boutique, cGMP compliant manufacturer.

H1B Sponsorship

Medivant Healthcare 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 (35)
2024 (13)
2023 (4)
2022 (6)
2021 (5)
2020 (1)

Funding

Current Stage
Growth Stage
Company data provided by crunchbase