Job Description

Title : GMP QA Supervisor

Shift : 3rd shift (Sunday - Thursday 11:00pm - 7:00am)

Duration : fulltime role - Direct hire

Location : Lancaster South Carolina 29720

Salary : $65,000 to $85,000/annually + 15% annual bonus

Benefits : Medical insurance/ Vision insurance/ Dental insurance/ Tuition assistance/ Disability insurance/ Childcare support/ 401(k)

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 of the day-to-day operations, techniques, and activities associated with those departments that are used to fulfill the Quality Assurance requirements of the product and/or service.

Roles and Responsibilities:

• The QA Supervisor is responsible for supervising those individuals within the QA department that include but are not limited to the following:
• QAG and Production process monitoring
• Responsible for Label Cage operations and personnel
• Protocol review
• Work with Production Supervisors to resolve production problems
• Review of SOPs
• Reviewing environmental conditions records and responding to excursions
• Assuring that all applicable cGMP requirements and regulations are met through compliance to government regulations, industry standards and company policies
• Conducting investigations, assessing and closing deviations, determining impact of the issues that could affect product quality, safety and purity.
• Reviewing of PMs, Pest Control, Calibration records, etc
• Working with Production, New Product Development, and other necessary departments to maintain awareness of Quality Systems activities.
• Product quality and conformance to government regulations, industry standards, and Company policies.
• Understanding and deploying processes to assure conformance to government regulations, industry standards and Company policies.
• Must periodically be able to work varying shift hours in support of personnel on those shifts.
• Must be able to effectively communicate with other departments and function within a team environment.
• Performance of other duties as assigned.

Minimum Requirements:

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

Education and Experience :

• BS Degree or BA Degree with a Science major or concentration and continuing education credits or certifications in the pharmaceutical industry through a reputable professional society.
• Minimum of 5 years' experience in Quality Assurance in the nutritional supplement and/or pharmaceutical products manufacturing industry.

Supervisory Responsibilities:

• Quality Assurance staff

Note: If interested please email me your resume at anil.chamoli@mastechdigital.com or call me at T: +1 617.848.2285 | C:+1 973.922.1844.

Best Regards,

Anil Chamoli

Team Lead ( Recruitment & Sales)

T: +1 617.848.2285 | C:+1 973.922.1844

Anil.Chamoli@mastechdigital.com

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