Auditing, Biology, Biotech and Pharmaceutical, Business Administration, Change Control, Chemistry, Communication Skills, Continuous Improvement, Control Systems, Corrective and Preventative Action (CAPA) Systems, Cross-Functional, Current Good Manufacturing Practice (cGMP), Drug Manufacturing, FDA Requirements, Healthcare, Leadership, Maintain Compliance, Manufacturing, Medical Equipment, Mentoring, Operational Improvement, Pharmacy, Project/Program Management, Quality Assurance, Quality Control, Quality Management, Regulations, Regulatory Compliance, Regulatory Requirements, Supply Chain, Validation Testing
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethical standards for the following position:
- Director of Quality (QA/QC)
Overview:
We are seeking an experienced Quality Director to lead and oversee all Quality Assurance and Quality Control functions at a pharmaceutical manufacturing site. This role ensures compliance with cGMP standards, regulatory requirements, and drives a culture of quality, continuous improvement, and operational excellence.
Key Responsibilities:
- Lead site-wide QA and QC operations, including batch release, testing, validation, and compliance
- Ensure adherence to FDA and global regulatory standards (cGMP)
- Oversee audits, inspections, CAPA, deviations, and change control systems
- Develop and implement quality strategies aligned with business objectives
- Build, mentor, and lead high-performing quality teams
- Partner cross-functionally with Manufacturing, Supply Chain, and Regulatory Affairs
Requirements:
- Bachelor’s degree in a scientific discipline (Chemistry, Biology, Pharmacy, or related)
- 8–10 years of pharmaceutical industry experience in QA/QC, with leadership responsibility
- Strong knowledge of cGMP, FDA regulations, and quality systems
- Proven track record managing audits and regulatory inspections
- Excellent leadership, communication, and decision-making skills
Preferred:
- Advanced degree (MS, PhD, or MBA)
- Experience in sterile or solid dose manufacturing environments
At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.
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Validation & Engineering Group, Inc