Senior Quality Control Associate

Life Science Recruitment; South Dublin; On-site; EUR 50,000 - 70,000; Full time

Job summary

A leading pharmaceutical organization based in Dublin is seeking a qualified individual for a Quality Control position. The ideal candidate will have a Bachelor’s degree in a science field and over 3 years of experience in biopharmaceutical quality control. Key responsibilities include performing analyses, ensuring compliance with regulations, and participating in audits. This role offers an exciting opportunity to work with a respected multinational company.

Qualifications

• Minimum 3+ years of biopharmaceutical QC experience.
• Strong background in Chemistry and Analytical testing.
• Experience with cGMP compliance in pharmaceuticals.

Responsibilities

• Plan and perform analyses efficiently and accurately.
• Report and approve analytical data.
• Participate in audits and implement changes.

Skills

Analytical testing

Troubleshooting

Data evaluation

Regulatory compliance

Education

Bachelor’s degree in a Science related field

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.

Duties:

• Plan and perform analyses with great efficiency and accuracy.
• Plan and perform multiple, complex routine/ non-routine methods and procedures and a large variety of assays.
• Report, evaluate, back-up/archive, trend and approve analytical data.
• Troubleshoot, solve problems and communicate with stakeholders.
• Initiate and/or implement changes in controlled documents.
• Participate in audits, initiatives and projects that may be departmental or organizational in scope.
• Review protocols and perform assay validation and equipment qualification/ verifications when required.
• Introduce new techniques to the lab, including method transfers, reports, validations and protocols.
• May contribute to regulatory filings.
• May conduct lab investigations as necessary.
• Evaluate lab practices for compliance on a continuous basis.
• Approve lab results.
• May interact with outside resources.
• LIMS data coordination of commercial and import testing on site where applicable
• May represent the department/organization on various teams. May train others.

Education and Experience :

• Bachelor’s degree in a Science related field is required.
• 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.
• Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.
• Experience with analytical techniques such as Compendial testing would also be advantageous