Demo

Quality Supervisor

Scientific Search
Petersburg, FL Full Time
POSTED ON 1/25/2025
AVAILABLE BEFORE 3/8/2025
Location: St. Petersburg, FL

Overview

Under the direction of the Plant Quality Manager, the Quality Supervisor has direct responsibility for implementing, maintaining, and facilitating continuous quality improvement objectives, primarily cGMP, ISO 13485 for site manufacturing. Responsible for quality control- in Process inspection and Product disposition activities, Material Review Board (MRB), NMRs and outside Product laboratory testing. Support environmental testing activities, the calibration program, SCARs, CAPAs, customer complaints investigations, Internal and External audits and drive continue improvements projects.

Responsible for supervising Quality Inspectors.

Evaluation of effectiveness of incoming, in-process, final inspection and process control mechanisms is an integral part of this position. Development of systems and procedures, training of personnel in the use of quality tools, identification of needed quality improvements and continual development, monitoring and reporting of key performance indicators is required.

Promotes a safe working environment, complies with proper use of PPE, reports incidents, and participates in functional department safety meetings. Exhibits good environmental practices and procedures consistent with job(s) performed and EMS (Environmental Management System) requirements.

Responsibilities

  • Supervise and lead Compounding and Testing Engineer, Technicians, and Lab functions.
  • Strategic planning for current and future laboratories, environmental testing and calibration program improvements.
  • Monitoring performance of assigned teams and programs/reporting results/elevating gaps.
  • Problem solving/data analysis/implementation of corrective actions.
  • Customer complaint investigation/audit finding investigation/providing audit support.
  • Creation and maintenance of policies, procedures and work instructions.

Requirements

  • Knowledge of and experience in Quality Systems ISO 13485, 9001, cGMP, and FDA requirements
  • Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.
  • Knowledge of and Experience in Quality tools (SPC, Statistical Analysis, Risk Management).
  • Strong organizational and communication skills, both written and verbal. Must have the ability to multitask. Strong technical writing and investigative skills.

Education

Bachelor’s degree in engineering and related field

The client offers a competitive salary package that is dependent on qualifications and experience, as well as a strong benefit package, plus participation in a company-wide bonus plan. For immediate consideration and faster response, please forward current resume to: sb@scientificsearch.com. Please include job #19104 in subject line. Please note that all candidates applying must be a US Citizen or Permanent Resident. Client will NOT sponsor.

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