Quality Assurance & QP Pathway – Dublin (Hybrid)

Next Generation

Dublin

Hybrid

EUR 65,000 - 90,000

Full time

36 hours ago
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Job summary

Next Generation in Dublin is seeking a Junior Qualified Person (QP) to join our Quality Assurance team. The role is hybrid (3 days onsite) with ~80% QA and 20% QP activities, offering hands-on training and a clear pathway to develop into a broader QP position.

You will support deviations, CAPAs, batch documentation review, product release, and inspections, ensuring EU GMP/GDP and MIA compliance while collaborating with global sites.

Qualifications

  • Degree in Science, Pharmacy or related discipline.
  • QP qualified/eligible or junior QP experience.
  • Strong pharmaceutical QA experience within a GMP environment.
  • Good knowledge of QMS, GMP/GDP and MIA requirements.
  • Experience with batch review/release and regulatory audits.
  • Strong communication and stakeholder management skills.
  • Comfortable combining hands-on QA responsibilities with developing QP duties.

Responsibilities

  • Manage and support pharmaceutical QMS activities including deviations, CAPAs and change controls.
  • Support QP activities, batch documentation review and product release.
  • Maintain compliance with EU GMP/GDP and MIA requirements.
  • Provide QA oversight of CMOs and external manufacturing partners.
  • Support HPRA inspections, regulatory audits and inspection readiness.
  • Support NPI, Quality Agreements and continuous improvement activities.
  • Collaborate with global manufacturing sites, affiliates and cross-functional teams.

Skills

QA experience
QMS
Regulatory audits
Stakeholder management
Communication

Education

Degree in Science/Pharmacy or related

Job description

Next Generation in Dublin is seeking a Junior Qualified Person (QP) to join our Quality Assurance team. The role is hybrid (3 days onsite) with ~80% QA and 20% QP activities, offering hands-on training and a clear pathway to develop into a broader QP position.

You will support deviations, CAPAs, batch documentation review, product release, and inspections, ensuring EU GMP/GDP and MIA compliance while collaborating with global sites.

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