Location: Dublin

About the company:

Innopharma Technical Services, part of Innopharma Group, specialises in the training and provision of highly skilled, project ready, Contract Engineers & Scientists to the (Bio) Pharmaceutical and MedTech Manufacturing Sector and provides recruitment support to our clients’ in these industries.

We are now seeking a Quality Technician – QC Analyst to provide support to our client site based in Dublin.

Role Type: Onsite role, no shifts.

About the position:

The Quality Technician – QC Analyst will be part of QC Department in a state-of-the-art, single-use, multi-product biotech facility in Dublin. The QC Analyst will support analytical testing across in-process, drug substance, drug product, and stability samples. The role focuses on Biochemistry and Cell Biology methods, ensuring full compliance with cGMP and corporate standards.

Key Responsibilities:

• Perform analytical testing (e.g., ELISA, PCR, bioassays, cell culture, compendial methods) in compliance with GMP
• Document, review, and approve laboratory data accurately
• Support laboratory operations including audit readiness, equipment qualification, calibration, and maintenance
• Participate in method transfer, validation, and verification activities
• Ensure adherence to SOPs, GLP/cGMP, and regulatory requirements
• Identify, investigate, and resolve deviations, non-conformances, and anomalies
• Contribute to continuous improvement initiatives using Lean principles and data-driven decision-making
• Maintain high standards of safety, including risk assessments and proactive hazard identification
• Collaborate across teams to solve problems and improve efficiency
• Participate in inspections, GEMBAs, tier meetings, and site walkdowns
• Support site strategy, value stream improvements, and project implementation
• Mentor/train team members and support knowledge sharing
• Maintain laboratory cleanliness, organisation, and material/sample control

Preferred Experience:

• Bachelor’s degree in Science, Quality, or related technical discipline
• Minimum of 3 yrs GMP laboratory experience in biotech/pharmaceutical industry
• Hands-on experience with analytical techniques (e.g., ELISA, PCR, bioassays) preferred
• Strong understanding of cGMP/GLP and regulatory compliance
• Excellent analytical, troubleshooting, and problem-solving skills
• Continuous improvement mindset with Lean knowledge (Lean Six Sigma desirable)
• High attention to detail and commitment to quality, safety (EHS Stds) and compliance
• Ability to manage multiple priorities and escalate issues appropriately
• Strong organisational and time management abilities
• Effective communication and collaboration skills
• Ability to work independently and within cross-functional teams
• Proactive, adaptable, and self-motivated.

Note:

• All applicants must be eligible to work in Ireland without Visa sponsorship.

Apply Now

If you’re passionate about manufacturing excellence and eager to grow in a fast-paced, regulated environment, we want to hear from you. Please send your CV to: [email protected]

Apply Now