Qc Analyst

PE Global (UK); Dunboyne; On-site; EUR 40,000 - 70,000; Full time

Job summary

PE Global (UK) is currently recruiting for a QC Analyst for a leading multi-national Pharma client based in Dunboyne. This contract position involves performing a variety of routine analytical techniques and associated documentation in compliance with GMP standards.

The ideal candidate will have a degree qualification in a relevant scientific field and 1-3 years of experience in the biotechnology or pharmaceutical industry, particularly with Capillary Electrophoresis, UPLC, HPLC, or GC testing. Strong problem-solving skills and a commitment to personal development are essential.

Qualifications

• Degree qualification (Science/Quality/Technical).
• 1-3 years’ experience in the biotechnology and/or pharmaceutical industry.
• Preferably Lean Six Sigma experience.
• Ability to think logically and be proactive under pressure.

Responsibilities

• Perform a variety of routine analytical techniques and documentation.
• Support activities including general lab readiness and audit readiness.
• Drive the development of technical skills through coaching.
• Foster continuous improvement and problem-solving capabilities.
• Deliver on specific area key performance indicators.
• Operate to the highest standards of safety, quality, and compliance.

Skills

Analytical techniques

Problem solving

GMP compliance

Lean Six Sigma

Education

Degree qualification in Science/Quality/Technical

Tools

Capillary Electrophoresis

UPLC

HPLC

GC

Job description

PE Global is currently recruiting for a QC Analyst for a leading multi-national Pharma client based in Dunboyne. This is a contract position.

Role

• Perform a variety of routine analytical techniques and associated documentation; including but not limited to Capillary Electrophoresis, UPLC, HPLC, GC, Wet Chemistry methods in compliance with GMP requirements
• Support activities including general lab readiness, audit readiness, laboratory equipment qualification and analytical method technical transfer, verification and validation
• Drive the development of technical skills through coaching and motivate a high performing culture across the team
• Foster a continuous improvement environment and bring strong problem solving and troubleshooting capabilities
• Consistently deliver on specific area key performance indicators
• Operate to the highest standards of safety, quality and compliance
• Demonstrate a commitment to learning and personal development that supports quality, EHS, L&D and continuous improvement

Requirements

• Degree qualification (Science/Quality/Technical)
• 1-3 years’ experience in the biotechnology and/or pharmaceutical industry, particularly in relation to Capillary Electrophoresis, UPLC, HPLC or GC testing
• Preferably Lean Six Sigma experience
• Ability to think logically and be proactive under pressure

Our client cannot assist with visa sponsorship, and candidates must have the correct visa to live and work in Ireland.