Senior Computer Systems QA Lead – MES & GMP Compliance

Life Science Consultants (LSC); Cork; On-site; EUR 60,000 - 80,000; Full time

Job summary

A biotech consulting firm is offering a contract opportunity for a Computer Systems QA Specialist in Cork, Ireland. The role requires a minimum of 5 years of relevant experience in a cGMP environment, along with expertise in lab systems and a strong background in validation and compliance. You will be responsible for quality leadership, managing quality-related matters, and promoting a culture of quality. Candidates must possess a Stamp 1G or 4 visa to apply.

Qualifications

• 5+ years of relevant experience in a cGMP environment.
• Expertise in lab equipment and lab systems.
• Strong background in validation and compliance.
• Skilled in project delivery and timeline delivery.

Responsibilities

• Provide Quality leadership for MES and related systems.
• Manage Quality-related matters specific to responsibility area.
• Approve quality-related documents to confirm compliance.
• Ensure compliance with site safety policies and report safety concerns.
• Promote Quality culture and report compliance concerns.

Skills

Lab Systems

QA Compliance

Project Delivery

Education

BSc, MSc or PhD in Chemistry, Engineering, or related discipline

Job description

A biotech consulting firm is offering a contract opportunity for a Computer Systems QA Specialist in Cork, Ireland. The role requires a minimum of 5 years of relevant experience in a cGMP environment, along with expertise in lab systems and a strong background in validation and compliance. You will be responsible for quality leadership, managing quality-related matters, and promoting a culture of quality. Candidates must possess a Stamp 1G or 4 visa to apply.