Quality Assurance Supervisor - 3rd shift, Plant 7
Perrigo Company is dedicated to making lives better by bringing high quality and affordable self-care products that consumers trust everywhere they are sold. Help us do it.
NOTE: This is a 3rd shift role based in Plant 7. Weekend coverage may be required on a rotational basis (1 weekend per month typically).
The QA Supervisor reports to the Quality Assurance Manger and primarily works to develop and maintain auditing methods which ensure identity control in raw materials, packaging, manufacturing and finished goods, with approval of final release of product for shipment. This position 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, planned deviations and supplier advisories. 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
The incumbent 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. The QA Supervisor Manages day to day work load of non exempt staff and manages shifting priorities to support internal & external customers, and Initiate and Executes and oversees projects as required.
- Bachelor’s degree, within a scientific discipline is strongly 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.
We are seeking a diverse applicant pool to ensure the diversity of our team reflects the end consumers we serve through our self-care mission. We are proud to be an equal opportunity employer that celebrates our team’s differences. Individuals of all races, ethnicities, nationalities, ancestries, religious creeds, sexual orientations, genders, gender identities and gender expressions, national origins, ages, mental and physical abilities, familial status,’ veterans status’, military status’ and more are encouraged to apply. TOGETHER, we make lives better.