Quality Assurance Supervisor (3rd shift)

Nutramaxlabs; Lancaster (SC); On-site; USD 60,000 - 90,000; Full time

Job summary

An established industry player is seeking a Quality Assurance Supervisor to lead a dedicated team in ensuring product quality and compliance within a dynamic manufacturing environment. This role offers the opportunity to oversee QA processes, collaborate with various departments, and ensure adherence to FDA regulations and industry standards. If you have a passion for quality assurance and a background in FDA-regulated environments, this position is perfect for you. Join a forward-thinking company committed to excellence in the nutritional supplement and pharmaceutical sectors.

Qualifications

• 3-5 years in FDA-regulated manufacturing, with 3 years in Quality Assurance.
• Experience in nutritional supplement or pharmaceutical manufacturing.

Responsibilities

• Supervise QA staff and ensure compliance with regulations.
• Conduct investigations and assess deviations impacting product quality.
• Collaborate with production supervisors to resolve issues.

Skills

Quality Assurance

FDA regulations

cGMP compliance

Team collaboration

Problem-solving

Education

BS or BA in Science

Continuing education in pharmaceuticals

Job description

Description

The hours for this position are Sunday - Thursday 11:15pm - 7:15am.

Summary of the Position: The Quality Assurance Supervisor reports to the Senior Quality Assurance Manager. This person supervises Quality Assurance Generalists and Label Issuance. The QA Supervisor supports all day-to-day operations, techniques, and activities associated with those departments to fulfill the Quality Assurance requirements of the product and/or service.

Roles and Responsibilities:

The QA Supervisor is responsible for supervising individuals within the QA department, including but not limited to:

• QAG and Production process monitoring
• Label Cage operations and personnel
• Protocol review
• Collaborating with Production Supervisors to resolve production issues
• Reviewing SOPs
• Reviewing environmental conditions records and responding to excursions
• Ensuring compliance with cGMP requirements, government regulations, industry standards, and company policies
• Conducting investigations, assessing deviations, and determining their impact on product quality, safety, and purity
• Reviewing PMs, Pest Control, Calibration records, etc.
• Working with Production, New Product Development, and other departments to maintain Quality Systems activities
• Ensuring product quality and conformance to regulations and standards
• Understanding and implementing processes to ensure compliance
• Periodically working varying shift hours to support personnel
• Communicating effectively with other departments and working within a team environment
• Performing other duties as assigned

Minimum Requirements: The QA Supervisor must have 3-5 years of experience in an FDA-regulated manufacturing environment, with at least 3 years in Quality Assurance or Quality Control. Prior FDA or equivalent inspection experience is highly recommended.

Education and Experience: BS or BA degree in a Science major or concentration, with continuing education credits or certifications in the pharmaceutical industry. A minimum of 5 years’ experience in Quality Assurance within the nutritional supplement and/or pharmaceutical manufacturing industry.

Supervisory Responsibilities:

• Supervising Quality Assurance staff
• Enforcing safe work practices and procedures, encouraging workers to identify hazards
• Correcting unsafe conditions within authority and ensuring timely follow-up
• Training employees to recognize and report hazards
• Reporting incidents, providing first aid, and ensuring medical treatment and emergency response as needed
• Completing incident reports, investigating, and coordinating corrective actions with EHS