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:

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

Full time, Shift work, Night shift, Sunday,