Senior QC Technician – MedTech, GMP & ISO 13485

Brighter Signals; Lancashire; Vor Ort; GBP 32.000 - 52.000; Vollzeit

Zusammenfassung

Johnson & Johnson is seeking a Senior Quality Control Technician in Blackpool, United Kingdom. The role focuses on QC testing, ensuring timely product release, and leading investigations in a GMP environment.

You will work across the lab to maintain compliance with ISO 13485 and FDA QMSR standards and support cross-functional teams. This position is tied to DePuy Synthes as part of a planned separation; (re)assignment will follow regulatory and works council processes.

Qualifikationen

• Minimum of A level in Science or mathematics discipline (international equivalents acceptable).
• Bachelor's degree in Scientific subject (Chemistry, Pharmacy, Forensics etc.) is desirable.
• Experience in a GMP regulated environment.
• Working with Microsoft Office applications (Word, Excel, PowerPoint, Office).
• Previous experience working within a quality environment in the Food, Consumer, Pharmaceutical or Medical device industry.

Aufgaben

• Physical testing of raw material, in process and finished product.
• Analytical testing of raw material, in process and finished goods.
• Chemical testing of raw material, in process and finished goods.
• Management of consumables and materials used in testing.
• Cleaning of items for testing within the laboratory.
• Execution of the laboratory cleaning program.
• Review of internal and external testing data.
• Lead investigations for Non-conformance and OOS excursions.

Kenntnisse

Administrative Support

Communication

Compliance Management

Document Management

Quality Control

Quality Standards

Quality Systems Documentation

Quality Validation

Teamwork

Execution Focus

Process Oriented

Factory Acceptance Test

Agility Jumps

Ausbildung

A level in Science or mathematics

Bachelor's degree in Scientific subject

Tools

Microsoft Office

Jobbeschreibung

Johnson & Johnson is seeking a Senior Quality Control Technician in Blackpool, United Kingdom. The role focuses on QC testing, ensuring timely product release, and leading investigations in a GMP environment.

You will work across the lab to maintain compliance with ISO 13485 and FDA QMSR standards and support cross-functional teams. This position is tied to DePuy Synthes as part of a planned separation; (re)assignment will follow regulatory and works council processes.