Biotech Plant Quality Assurance Analyst

2 weeks ago

Dublin, Dublin City, Ireland JobContax Full time

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Biotech Plant Quality Assurance Analyst - Shift, Dublin

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Client:

JobContax

Location:

Dublin, Ireland

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

f5961a7c558d

Job Views:

7

Posted:

19.08.2025

Expiry Date:

03.10.2025

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Job Description:

Biotech Plant Quality Assurance Analyst - Dun Laoghaire, Dublin

Employment Type: Contract

Experience: 4+ years

Visa:EU passport or Stamp 4 visa required

Our client is a leading international Biotechnology company with a state of the art aseptic manufacturing facility in Dun Laoghaire, South Dublin.

The plant is one of the most dynamic in Ireland and is currently undergoing rapid expansion and capital investment.

This is an excellent opportunity to get experience into Ireland's leading aseptic manufacturing plant.

The Senior Associate for Plant Quality Assurance (PQA) will report to the QA Manager, playing a pivotal role in the site's Quality Assurance team.

As the Quality point of contact for manufacturing and inspection operations, you will contribute to continuous improvement initiatives by undertaking additional responsibilities beyond routine QA duties.

Ensure adherence to safety standards and SOPs in all activities.

Review and approve production batch records and associated documentation for Qualified Person disposition activities.

Provide real-time quality oversight and support for production unit operations, extending to formulation, vial and syringe Fill Finish activities, including media fills and assessment of aseptic interventions.

Conduct inspections of vials and syringes as part of AQLs, annual reserve inspections, and support complaint investigations.

Offer Quality Assurance support for on-the-floor investigations and deviations.

Review and approve deviations for closure, ensuring compliance with appropriate documentation.

Participate in customer complaint investigations.

Conduct routine Quality Assurance walks on the production floor.

Review and issue logbooks, ensuring compliance with procedures.

Provide training and guidance to staff for effective performance.

Review and approve cGMP records, ensuring compliance with appropriate documentation.

Support continuous improvement and Operational Excellence initiatives.

Undertake other tasks/projects as assigned by the manager

Requirements

University degree in an Engineering or Science-related discipline (preferred).

Over 4 years of relevant experience in the pharmaceutical or biotechnology industry or an equivalent combination of experience and educational background.

Exceptional written and verbal communication skills.

Proven experience collaborating with dynamic cross-functional teams and strong decision-making abilities.

Robust organizational skills, with a commitment to seeing assignments through to completion.

Demonstrated problem-solving abilities, particularly in supporting non-conformance/deviation investigations.

Experience in inspecting vials and syringes and engaging in aseptic operations.

Familiarity with applicable Regulatory requirements and proficiency in evaluating compliance issues

Package

Minimum 12 month contract with the possibility of an extension.

Onsite role

Shift Details: This 24/7 shift role demands a 12-hour shift pattern (4 on, 4 off) to support manufacturing operations.

Hours: 07:00 to 19:00, and 19:00 to 07:00.

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