Director, QC/QA- Dietary Supplements
4 weeks ago
NeoLife is a nutrition company that has been in business for 65 years and operating in over 50 countries around the world. We offer superior quality products using nature's finest whole food ingredients that are based in nature and backed by leading edge science. We are on a mission to make the world a healthier and happier place. We believe that because people matter, health and wellness should matter. This position is in our Natural Formulas Manufacturing Division which is located in Hayward, California. POSITION SUMMARY: he Quality Director oversees the operational aspects of the Quality Control and Quality Assurance Department relating to the manufacture, testing, and distribution of products in strict accordance with Standard Operating Procedures, current Good Manufacturing Practices, FDA food and dietary supplement regulations. JOB RESPONSIBILITIES:
- Responsible for overseeing the execution of raw material and finished good testing for NeoLife's domestic and international markets.
- Responsible for interpreting the results of all testing and reporting any issues to VP and to the Research & Development team.
- Collaborate with VP and Research & Development team to reject product releases and write deviations when appropriate.
- Responsible for overseeing the development of necessary documentation including SOPs, analytical testing documentation, and product dossiers.
- Manage stability studies including creating stability protocols, placing new and reformulated products in stability, and performing technical review of stability test results.
- Responsible for the operation of a Material Board Review for raw material substitutions, shelf-life extensions, and rejections.
- Collaboration with internal personnel and outside consultants to ensure accuracy and compliance of domestic and international labels.
- Responsible for identifying problems, developing solutions, and executing the appropriate course of action in collaboration with VP and Research & Development team.
- Bachelor of Science Degree in chemistry, biochemistry, biochemical engineering, life science, or related field. Master's Degree preferred.
- 6-8 years or more of Quality Management experience in a manufacturing environment for Dietary Supplement products.
- Demonstrated abilities to develop and supervise Quality Control and Quality Assurance laboratory personnel.
- Understanding and knowledge of dietary supplement cGMPs, 21 CFR part 111.
- Strong Knowledge of Quality Systems Design and Implementation.
- Must have experience with document control systems and processes and product release procedures including testing deviations.
- Experience in working with the Purchasing and R&D teams in the development and implementation of raw material specifications and finished good specifications to safeguard consistent supply chain and to ensure the integrity of the product design.
- Skilled and strategic manager, strong technical and analytical skills.
- Attention to detail, critical-thinking skills, superior organizational skills.
- Excellent verbal and written skills.
- Ability to assimilate information and act quickly.
- Proficiency in Microsoft Office Suite of applications (Word, Excel, Outlook)
Compensation details: 00 Yearly Salary
PIc248206ce2d3-9972
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