Qualified Person QA Specialist – Dublin (Hybrid)

Worklane GmbH

Dublin

Hybrid

EUR 95,000 - 130,000

Full time

14 days+
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Job summary

Bausch + Lomb Ireland Limited is seeking a Quality Assurance professional to act as European Qualified Person with responsibility for managing the QMS, ensuring GMP compliance, and supporting BLIL authorisations and HPRA interactions. Hybrid role with three onsite days in City West, Dublin.

Key requirements include a BSc in science, a QP qualification, and at least five years in QA within healthcare. Strong communication, initiative, and attention to detail are essential to drive continuous

Qualifications

  • BSc (Hons) in Science or equivalent.
  • QP qualification.
  • Thorough working knowledge of GMDPs and regulatory expectations for medicinal products and medical devices.
  • Minimum of 5 years of experience working in Quality Assurance in the Health Care Industry.
  • Good communication skills
  • The ability to motivate and influence people
  • Self-starter, highly motivated with the ability to prioritize
  • Ability to work on own initiative
  • High attention to detail
  • Good team member Excellent ability to deliver results, with strong interpersonal and influencing skills.

Responsibilities

  • Manage the QMS, ensure the QMS is fit for purpose, making changes as necessary approving SOPs and Quality System documents.
  • Maintain Quality processes in support of BLIL authorizations (WDA, MIA)
  • Ensure processes are maintained in support of BLIL as MAH
  • Participate in managing communications with and represent BLIL in front of HPRA.
  • Provide QA expertise to BLIL and manage any Quality issues that arise to closure.
  • Support HPRA inspections of BLIL and prepare written responses to inspections.
  • Support Bausch + Lomb internal compliance audits of the BLIL operations.
  • Prepare and approve HPRA variations.
  • Provide QA oversight and expertise for New Product Introductions.
  • Initiate / approve Non-Conformances (NC), CAPA, change controls and complaints.
  • Ensure annual review of supplier and customer bona fides to verify compliance with Guidelines on Good Distribution Practice.
  • Ensure Batch record review to verify compliance with GMP and Market Authorization prior to batch release.
  • To approve or reject finished products.
  • Ensures that each finished medicinal product batch has been manufactured in accordance with GMP and the MA.
  • Review, and where appropriate, preparation and regular update of technical agreements with licensees and 3rd party contractors.
  • Periodic review of QMS and operational procedures for regulatory compliance through internal audit system.
  • Participating in periodic Quality Operations management review meetings with third parties, annual Quality Management Review meetings, and participating in preparing the agenda and minutes for both meetings.
  • Attending the annual Quality Management Review meeting and participating in the review of the BLIL Quality and Regulatory Compliance Policy and Objectives for continuing suitability.
  • Implementation of the Self Inspection/Internal Quality Audit program.
  • Overall responsibility for reporting and investigation of non-conformances and identification of CAPAs to ensure continuous improvement of the QMS and operational procedures.
  • Escalation of issues as appropriate.
  • The QP must be eligible to act as a European Qualified Person (QP), certifying products in compliance with 2001/83/EC, 2003/94/EC and Annex 16.

Skills

Communication
Motivation & influence
Self-starter
Initiative
Attention to detail
Interpersonal skills

Education

BSc (Hons) in Science or equivalent
QP qualification

Job description

Bausch + Lomb Ireland Limited is seeking a Quality Assurance professional to act as European Qualified Person with responsibility for managing the QMS, ensuring GMP compliance, and supporting BLIL authorisations and HPRA interactions. Hybrid role with three onsite days in City West, Dublin.

Key requirements include a BSc in science, a QP qualification, and at least five years in QA within healthcare. Strong communication, initiative, and attention to detail are essential to drive continuous

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