• Supervise and coach staff using the performance management process
• Hiring and training new staff quality production staff
• Assist in achieving quality department goals and objectives, striving for continuous improvement.
• Maintain the Environmental Monitoring Program.
• Facilitate the annual Cleaning and Blend Validation Program.
• Support compliance programs to ensure compliance by all employees in the manufacturing facility.
• Ensure the accuracy and integrity of batch paperwork and samples.
• Report on Team Key Performance Indicators (KPIs).
• Support the non-conforming Materials product program, managing the status, release, and destruction of “Rejected” products.
• Assist in investigating and correcting quality-related issues
• Aid in root cause analysis and corrective action implementation.
• Initiate Control Document revisions as needed to ensure compliance and continuous improvement.

• B.S. Degree in a Life Science or Equivalent in experience
• 2-5 years of Quality Assurance Experience within a cGMP regulated manufacturing environment.
• Pharmaceutical, Food or Biotechnology manufacturing experience is a plus!
• 1-2 years of experience within supervision, training, or performance evaluations
• Experience with FDA/cGMP compliance.

• Medical, dental, vision, short term disability, accident insurance, critical illness insurance, and life insurance plans.
• 401k plan with company matching funds, FSA, and tuition reimbursement.
• PTO for employees include holidays and vacation

*This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you**
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