Job Title:
Quality Supervisor

Req #:
4651BR

Job Description:
Provide oversight for receiving inspection, managing routine workflow to ensure component availability to manufacturing. Identify opportunities for process improvements, cost reduction, and risk mitigation activities. Provide input into specification requirements for new components and measurement techniques. Assist in investigation of product/process non-conformances. Provide oversight for QA Release function, managing routine workflow to ensure product releases are performed according to schedule. Identify opportunities for process improvements, cost reduction, and risk mitigation activities. Assist in investigation of product/process non-conformances. Provide oversight for calibration function, managing routine workflow to ensure calibrations are performed according to schedule. Identify opportunities for process improvements, cost reduction, and risk mitigation activities. Provide supervisory oversight for groups, including managing scheduling, time cards, vacation approvals, and personnel discipline/reviews. Manage Material Review Board (MRB) process, ensuring timely disposition of nonconforming product. Track metrics related to supplier performance in support of SBMT, management review. Track metrics related to calibration for management review. Track metrics related to product release as needed to maintain process flow.

Qualifications
Bachelors degree strongly preferred. 5-7 years demonstrated experience as a supervisor. Previous medical device or pharmaceutical manufacturing experience highly desirable. Supervisory experience within a QA role strongly preferred. Good organizational skills a must. Effective communication skills needed to provide clear and concise information to team members. Demonstrated knowledge of computers to include email, excel and word.

Work Location FL - Clearwater Relocation Available Yes

Status Full-Time