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Quality Assurance Specialist - Dublin North

Recruitment Plus

  • Louth / Dublin City Centre / Dublin North
  • Negotiable
  • Permanent full-time
  • Updated 04/10/2017
  • Zuzana Foley
this job is expired
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Quality Assurance Specialist - Dublin North - D004840 Please hit the apply now button above and Zuzana who is based in our Dundalk office will be in contact if you are suitable.


Quality Assurance Specialist - Dublin North - D004840

Recruitment Plus is currently recruiting for a Quality Assurance Specialist, in Dublin North who will be responsible for the review and assessment of data and cGMP documentation generated within the QA Specialist perform a variety of pharmaceutical operations support tasks including but not limited to Production Support, batch paperwork review and Quality Systems support (e.g. Deviations, CAPAs, PQR, Change Control, etc.).

Depending on the primary area of focus the incumbent oversees and utilizes systems such as TrackWise and SAP and other software applications, as needed. Specialists are responsible for writing, reviewing and approving investigations, protocols and reports.

Specialists perform production support, monitoring, sampling activities and internal audits as required. The QA Specialist is expected to adhere to all cGMP compliance and regulatory mandates and quality requirements, and comply with all SOPs and internal organisation policies and procedures in the performance of job duties. The QA Specialist applies skills and knowledge to recognize and resolve issues that impact efficiency, throughput, quality, and/or the fulfilment of the assigned performance targets. The QA

Specialist is responsible for the safe, compliant, and efficient execution of job duties in a team environment. This position reports to the QA Supervisor and/or QA Team Lead as applicable.

Location: Dublin North, commutable from Meath, Louth, Dublin South, Dublin City, Dublin West.


  • Bachelor's Degree required. Chemistry or Life Science degree preferred. Some exceptions made for those candidates demonstrating equivalent knowledge and having pharmaceutical experience.
  • Prior pharmaceutical or quality assurance experience preferred but not required.
  • Knowledge of GMP (Regulations including EU, Cosmetics Directive, Medical Device Directive desirable)
  • May participate in department initiatives and projects.
  • Strong analytical skills and knowledge of quality systems.
  • Demonstrated written and verbal communication skills.

Please hit the apply now button above and Zuzana who is based in our Dundalk office will be in contact if you are suitable.

Unfortunately, Recruitment Plus is not in a position to respond to each individual application due to the high volume of submissions. We will only contact those candidates whose CV matches the criteria for the vacancy. Thank you for your patience.

At RecruitmentPlus, we respect your privacy. Your CV is sent to us in complete confidence and will never be forwarded to a third party without your consent.

Ref: D004840
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