Role OverviewOversee the day-to-day operations of the Quality Assurance Department, including internal and external audits, document control, compliance, GMP training, SOP development and control, and other related programs. Identify continuous improvement activities to enhance and sustain GMP compliance in the production of Dietary Supplements and other IVC products.
What You Will Do
Enforce GMP compliance, review and develop quality system policies and procedures, maintain and implement the company's quality system policies and procedures, develop and update standard operating procedures (SOPs), participate in external audits, and prepare quality reports.
Why It Might Be a Fit
Requires 2-5 years of experience and a Bachelor's degree in a related field or equivalent job experience. Must have minimum 5-10 years of experience establishing and maintaining quality systems in the Dietary Supplements and/or pharmaceutical manufacturing industry with 3+ years in a Supervisory role.
Requirements
- Bachelor's degree in a related field or equivalent job experience
- 2-5 years of experience
- Minimum 5-10 years of experience establishing and maintaining quality systems in the Dietary Supplements and/or pharmaceutical manufacturing industry with 3+ years in a Supervisory role
- Computer literate and familiar with commercial software such as Microsoft Office: Word, Excel, Access, and PowerPoint
- Knowledge of 21 CFR 110 and 111 quality regulations and current Good Manufacturing Practices (cGMP) guidelines
- Ability to work in a manufacturing environment with air-borne powder, noise, and moving equipment
- Able to communicate, write, and understand English
- Ability to sit, walk, stand, and reach frequently
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