Senior Technician Quality Control

Life Science Recruitment; Carlow; On-site; EUR 38,000 - 52,000; Full time

Job summary

Life Science Recruitment Ltd is seeking a Senior Technician Quality Control for an onsite, 11-month contract in Carlow. The role supports cGMP compliant QC activities, testing and release of vaccine and biologic products, and close collaboration with Quality, QC and Manufacturing teams.

The ideal candidate holds a degree in Science or Engineering, with 2–4 years in pharma/biopharma, and a Lean Six Sigma Yellow Belt.

Qualifications

• Degree in Science, Engineering or similar.
• 2-4 years’ experience in Pharmaceutical, Biopharmaceuticals or similar operating environment with a Quality function.
• Lean Six Sigma Yellow Belt or suitable alternative.
• Knowledge of cGMP in Laboratory Quality Systems.
• Proficiency in Microsoft Office and job-related computer applications required

Responsibilities

• Ensure compliance with cGMP, GDP, data integrity (ALCOA) and regulatory requirements across all Quality activities.
• Support the manufacturing, testing and release of vaccine and biologic products in accordance with site procedures and regulatory standards.
• Collaborate with Quality, QC, Manufacturing and other departments to resolve quality-related queries and maintain compliance.
• Identify and support continuous improvement and compliance initiatives to enhance operational efficiency.
• Support business-critical projects within the Quality Department.
• Perform laboratory testing, including analytical and microbiological testing, and material inspections to ensure specification conformance.
• Maintain a safe, compliant and qualified laboratory environment, adhering to PPE and safety requirements.
• Execute, review and support deviations, CAPAs, complaints, material qualification, validation and Quality Risk Management activities.
• Review batch records, material documentation, SOPs, GMP data and other quality-related documentation.
• Support the development, revision and implementation of SOPs, operational procedures and training materials.
• Participate in training activities and provide support to team members as required.
• Work shift patterns where required to support manufacturing and Quality operations.

Skills

cGMP knowledge

Data integrity (ALCOA)

Analytical testing

Microbiological testing

Quality documentation

Education

Degree in Science/Engineering or similar

Lean Six Sigma Yellow Belt

Tools

Microsoft Office

Job description

Senior Technician Quality Control
Onsite - Shift 2 cycle
RK26656
Contract 11 months
Carlow
We’re currently recruiting for an exciting opportunity with an award-winning pharmaceutical organization based in Carlow. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.

Key Responsibilities:

• Ensure compliance with cGMP, GDP, data integrity (ALCOA) and regulatory requirements across all Quality activities.
• Support the manufacturing, testing and release of vaccine and biologic products in accordance with site procedures and regulatory standards.
• Collaborate with Quality, QC, Manufacturing and other departments to resolve quality-related queries and maintain compliance.
• Identify and support continuous improvement and compliance initiatives to enhance operational efficiency.
• Support business-critical projects within the Quality Department.
• Perform laboratory testing, including analytical and microbiological testing, and material inspections to ensure specification conformance.
• Maintain a safe, compliant and qualified laboratory environment, adhering to PPE and safety requirements.
• Execute, review and support deviations, CAPAs, complaints, material qualification, validation and Quality Risk Management activities.
• Review batch records, material documentation, SOPs, GMP data and other quality-related documentation.
• Support the development, revision and implementation of SOPs, operational procedures and training materials.
• Participate in training activities and provide support to team members as required.
• Work shift patterns where required to support manufacturing and Quality operations.

Education and Experience:

• Degree in Science, Engineering or similar
• 2-4 years’ experience in the Pharmaceutical, Biopharmaceuticals industry or a similar operating environment which includes experience in a Quality function.
• Lean Six Sigma Yellow Belt or suitable alternative
• Knowledge of cGMP in Laboratory Quality Systems.
• Proficiency in Microsoft Office and job-related computer applications required