What are the responsibilities and job description for the Quality Operations Supervisor position at Pharmatech, Inc.?
At Pharmatech, providing an unrivaled customer experience as a nutritional product manufacturer is our vision. We are committed to building a positive, diverse, accountable and supportive culture centered on integrity and continuous improvement. If this aligns with your values, we invite you to join our team!
The Quality Assurance Supervisor is a key role in the organization with responsibility to manage a team of Quality Assurance Technicians, ensuring quality, safety, and regulatory compliance throughout the sampling, manufacture, and release processes.
RESPONSIBILITIES
- Effectively manage Quality Assurance team providing training and support as needed
- Train staff on procedures for compliance with cGMP, HACCP, Food Defense, and other important standards.
- Support company and product certifications (NSF, NSF for Sport, SQF, Kosher, Non-GMO, Organic, etc.)
- Ensure compliance with FDA, Department of Health, and certifying body requirements
- Participate in internal and external audits (regulatory, certification, and customer)
- Review and update SOPs, policies, and processes regularly to ensure cGMP
- Support team in sampling, in-process verifications, and product release
- Member of the Material Review Board (MRB)
- Participate in aspects of the Quality Management System (QMS)
- Communicate effectively with internal and external customers
- Other duties as assigned
WORKING RELATIONSHIP
- Reports to the Director of Quality / Technical Services
- Actively fosters the Pharmatech culture in word and deed
- Work closely with Quality Control, Regulatory Compliance, and Operations teams
- Partners directly with all departments to ensure compliance to quality standards and regulatory requirements
- Strives to continuously build knowledge and skills and shares expertise with others
QUALIFICATIONS REQUIRED
- Demonstrated success in leadership role (3 years)
- Experience in FDA regulated industry (Dietary Supplement, Food, Medical Device, etc.)
- Understanding of regulatory requirements; reference 21 CFR 110, 111, and 117
- Facility and product certification experience preferred (NSF, TGA, SQF and GFSI)
- PCQI, CQA, and similar certifications preferred
- Excellent interpersonal and communications skill
- Bilingual skills (Spanish/English) preferred
EDUCATION
- Bachelor of Science degree or commensurate experience
Salary : $55,000 - $70,000