Senior Quality Supervisor — Medical Device Manufacturing

Dielectrics, a UFP Technologies company

Providence (RI)

Vor Ort

USD 65.000 - 95.000

Vollzeit

vor 25 Stunden
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Health benefits
401K with match
Paid time off
Employee discounts

Zusammenfassung

Contech Medical, a UFP Technologies company, seeks a Quality Supervisor to lead the on-site QA/QC team in Providence, RI. You will ensure only material meeting specifications leaves the facility and drive improvements to inspection plans.

You will supervise testing, analyze data, manage documentation, and ensure adherence to cGMP and ISO 13485. Strong communication and leadership are essential to develop and coach staff.

Qualifikationen

  • Bachelor’s degree or equivalent work experience in a lead QA/QC role.
  • 5+ years’ experience in QA/QC preferred, medical device manufacturing a plus.
  • ASQ certification is preferred.
  • Excellent communication skills and a track record of developing subordinates.
  • Strong analytical skills with detail orientation and ability to work independently.

Aufgaben

  • Oversees quality control testing, sampling, and control strategies.
  • Performs inspection and testing when necessary.
  • Analyzes product and process quality data to meet quality objectives.
  • Audits QC staff for quality and quantity of work performed.
  • Manages material release and final disposition activities.
  • Establishes measurement systems analysis processes for QC.

Kenntnisse

Communication
Analytical thinking
Detail orientation
Independent work
Supervisory ability

Ausbildung

Bachelor’s degree
ASQ certification

Tools

Word
Excel
ERP systems

Jobbeschreibung

Contech Medical, a UFP Technologies company, seeks a Quality Supervisor to lead the on-site QA/QC team in Providence, RI. You will ensure only material meeting specifications leaves the facility and drive improvements to inspection plans.

You will supervise testing, analyze data, manage documentation, and ensure adherence to cGMP and ISO 13485. Strong communication and leadership are essential to develop and coach staff.

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