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QA Supervisor FDA Industry - 3rd Shift

Job Type
Location
Lancaster, South Carolina
Salary
US$75000.00 - US$85000.00 per annum + 15% bonus, relocation, tuition
Job Ref
BBBH2307024_1719507953
Date Added
June 27th, 2024

SRG, the leader in the Life Sciences human capital industry, is looking for a full-time permanent Quality Assurance Supervisor - 3rd shift to join their client's team in Lancaster, SC. 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.

JOB RESPONSIBILITIES include, but are not limited to:

  • Supervising those individuals within the QA department
  • Working on the floor in production most of the night, overseeing the direct reports
  • Completing Quality checks, packaging checks, oversee quality of raw materials checks, QC checks of weights
  • QAG and Production process monitoring
  • Responsible for Label Cage operations and personnel
  • 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.

WHAT YOU NEED TO HAVE:

  • Supervisor experience of QA staff with direct reports
  • Long term commitment to the company
  • Excellent communication and ability to show teamwork and leadership
  • 5 years' experience in Quality Assurance in the FDA regulated nutritional supplement and/or pharmaceutical products manufacturing industry.
  • cGMP knowledge and experience
  • Bachelor's degree in science or relevant experience
  • Available for 3rd shift position - Sun-Thur 11:15pm to 7:15am

* Only candidates selected to be moved forward in the recruitment process will be contacted by SRG's Recruitment Team to schedule a conversation.

Impellam Group and its brands are equal-opportunity employers committed to diversity and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, gender, sexual orientation, pregnancy or maternity, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application, interview process, pre-employment activity, and the performance of crucial job functions.

If you require additional disability considerations, modifications, or adjustments please let us know by contacting HR-InfoImpellamNA@impellam.com or fill out this form to request accommodations.

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