Full-Time
Director of Quality
Confirmed live in the last 24 hours
Technical services for pharmaceuticals, nutrition supplements
Industrial & Manufacturing
Senior, Expert
Pensacola, FL, USA
Required Skills
PowerPoint/Keynote/Slides
Requirements
- Bachelor’s degree in science or related field; Master’s degree preferred
- 8+ years of experience in Quality Control or Quality Assurance in pharmaceutical manufacturing and 5+ years of experience leading Quality teams. Experience working with cGMP, DEA, USP, FDA, and EP agencies required.
- 5+ years of experience in Quality Control or Quality Assurance in the animal health industry
- Proficient with Microsoft Office Suite, including Word, Excel, PowerPoint, Outlook)
- Experience with QMS and ERP Systems; Master Control preferred
Responsibilities
- Hire, coach, and develop department leaders, and hold accountable for staffing, training, and developing the functional downstream leadership teams.
- Evaluate effectiveness of measurement systems and performance indicators to include but not limited to skills matrix, scorecards, and KPIs for continuous improvement.
- Responsible for developing overall department budget. Hold functional leaders accountable to meet or exceed individual expense budget expectations that include equipment, headcount, and new projects.
- Ensures all products manufactured are produced, tested, and released in compliance with cGMP, SOP, FDA, and EU regulations.
- Makes decisions regarding quality control and compliance for batches and for new and/or existing products, including discrepant batches (investigations, retesting, and re-inspections), and manages the review of compliance investigations.
- Oversee procedures and specifications affecting product quality (e.g. batch records, SOP, validation protocols and reports) to ensure quality compliant products are released to market.
- Supports inspections by FDA, EU, DEA, State and other regulatory agencies as secondary point of contact and partners with Regulatory to prepare inspection and observation responses.
- Review and approve all facility and equipment changes that may affect cGMP.
Pegasus Laboratories specializes in providing technical services for pharmaceutical products and nutritional supplements, operating in a cGMP facility with DEA approval and utilizing state-of-the-art manufacturing and laboratory facilities to support their services.
Company Stage
N/A
Total Funding
N/A
Headquarters
Pensacola, Florida
Founded
1986
Growth & Insights
Headcount