Senior QC Specialist - GMP Lab, MedTech

Biopharma Asia; Lancashire; Hybrid; GBP 32,000 - 42,000; Full time

Job summary

Johnson & Johnson in Blackpool, United Kingdom, is seeking a Senior Quality Control Technician to ensure product quality and lead lab investigations. You will perform QC testing on raw materials, in-process samples, and finished products, supporting timely release and compliance with cGMP and regulatory standards.

The role requires a strong background in quality control within pharma/medical devices, with hands-on testing and data review, plus collaboration with cross-functional teams to drive

Qualifications

• Minimum of A level in Science or mathematics (international equivalents acceptable).
• Bachelor's degree in Chemistry, Pharmacy, or related scientific field desirable.
• Experience in a GMP-regulated environment.
• Proficient in Word, Excel, PowerPoint; familiarity with LMS/quality systems is a plus.
• Previous experience in a quality environment in pharma/medical devices is preferred.

Responsibilities

• Day to day performance: 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.

Skills

Quality Control

Compliance

Documentation

Analytical Thinking

Attention to Detail

Communication

Teamwork

Education

A level in Science or Mathematics

Bachelor's degree in a Scientific subject

Tools

Microsoft Office

Job description

Johnson & Johnson in Blackpool, United Kingdom, is seeking a Senior Quality Control Technician to ensure product quality and lead lab investigations. You will perform QC testing on raw materials, in-process samples, and finished products, supporting timely release and compliance with cGMP and regulatory standards.

The role requires a strong background in quality control within pharma/medical devices, with hands-on testing and data review, plus collaboration with cross-functional teams to drive