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Quality Assurance Supervisor - 2nd Shift, LVS

Description

Perrigo Company plc, a leading global healthcare company, delivers value to its customers and consumers by providing Quality Affordable Healthcare Products. Founded in 1887 as a packager of home remedies, Perrigo has built a unique business model that is best described as the convergence of a fast-moving consumer goods company, a high-quality pharmaceutical manufacturing organization and a world-class supply chain network. Perrigo is the world's largest manufacturer of over-the-counter ("OTC") healthcare products and supplier of infant formulas for the store brand market. The Company also is a leading provider of branded OTC products throughout Europe and the U. S., as well as a leading producer of "extended topical" prescription drugs. Perrigo, headquartered in Ireland, sells its products primarily in North America and Europe, as well as in other markets, including Australia, Israel and China.

The Quality Assurance Supervisor develops and maintains auditing methods which ensure identity control in raw materials, packaging, manufacturing and finished goods, with approval of final release of product for shipment. Reviews and approves controlled documents, including SOPs, SWIs (Standard Work Instructions), Job Aids, SCRF (SAP Change Request Form), SBRF (Split Batch Request Form), RW s (Rework) Notifications and planned deviations. Coordinates initial response activity including risk assessment and containment for Quality Events. Identifies any non-conformances or variances, recommends corrective action, and ensures follow up actions are taken by working with staff and management in those areas. Manages/trains non-exempt staff to ensure that all documentation meets cGMP and FDA standards. Assists with FDA inspections as requested and ensures FDA readiness in Operations. Also, assists with 3rd party Audits (Customer, Contract). Selects, mentors, and evaluates performance of non-exempt staff and provides quality coaching and guidance to floor level operations. Manages day to day work load of non-exempt staff and manages shifting priorities to support internal & external customers. Initiates, executes and oversees projects as required.

Requirements:

  • Bachelor s degree, within a scientific discipline preferred. Consideration may be given to non-degreed candidates who meet all other qualifications and possess considerable quality assurance or manufacturing and packaging process knowledge in a regulated environment.
  • Good oral and written communication skills, and excellent interpersonal skills.
  • Previous experience working in an FDA regulated industry preferred.
  • Previous experience ensuring the quality of products and or manufacturing/packaging processes.
  • Previous leadership experience highly preferred.
  • Ability to interpret and apply formal regulations to product quality and processes.
  • Familiarity with cGMP, quality assurance, release methods, auditing and/or risk assessment in an FDA regulated environment highly preferred.
  • Knowledge of SAP preferred.
  • Weekend coverage is required.

We're proud to be an equal opportunity employer- and celebrate our employees' differences, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or Veteran status. Different makes us better.

Due to the highly regulated pharmaceutical industry and legal requirements, you may be subject to post employment background checks.



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