Senior Quality Control Associate

Life Science Recruitment; Leinster; On-site; EUR 45,000 - 65,000; Full time

Job summary

Life Science Recruitment in Dublin is seeking a QC Representative for an award-winning pharmaceutical organisation. You will support NPI activities, participate in product meetings, and oversee non-core testing, sample handling, and SOP documentation to ensure GMP alignment.

Required are 2–3 years in biopharmaceutical QC, strong chemistry/analytical testing skills (HPLC), and regulatory cGMP experience. The role involves LIMS data coordination, method validation support, and safety training

Qualifications

• 2–3 years of biopharmaceutical QC experience or related GMP lab experience.
• Strong background in Chemistry and Analytical testing is required (HPLC).
• Experience with regulatory compliance in cGMP manufacturing and testing.

Responsibilities

• QC Representative for NPI activities and routine Product meetings.
• Assist with QC projects and tasks within site projects.
• Plan and perform non-core testing related to NPI activities.
• Manage sample management for NPI activities across the site.
• Create/own and approve protocols, sample plans, SOPs and documentation for NPI.
• Coordinate Method Validation and Transfers readiness.
• Ensure training and safety compliance for own role.
• Handle sample shipments and temperature monitoring for NPI.
• Coordinate LIMS data for non-core NPI activities.

Skills

QC experience

GMP knowledge

Analytical testing

Regulatory compliance

Tools

LIMS

HPLC

Job description

We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin. 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:

• QC Representative for NPI activities and routine Product meetings
• Assist with activities related to QC projects and/or QC tasks within Site projects
• Plan and perform non-core testing related to NPI activities
• Manage all sample management activities related to NPI activities throughout the site
• Create/own and approve protocols, sample plans, SOP and documentation related to NPI
• QC Representative responsible for Method Validation and Transfers co-ordination and readiness
• Responsible for their own training and safety compliance.
• Sample shipments and temperature monitoring activities for NPI activities
• LIMS data coordination of non-core (NPI) activities.

Education and Experience:

• 2-3 years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry.
• Strong background in Chemistry and Analytical testing is required – HPLC and High Volume Testing experience
• Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.