Quality Technician – QC Analyst (Biochemistry & Cell Biology)
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