Senior QA Operations Leader — Pharma Quality Excellence

R&D Partners

Munster

In loco

EUR 110.000 - 140.000

Tempo pieno

12 ore fa
Candidati tra i primi
Generatore di candidature

Non inviare un curriculum generico — genera un curriculum e una lettera di presentazione personalizzati per questo specifico impiego.

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Descrizione del lavoro

R&D Partners in Ireland is seeking a Senior Manager in Quality Assurance Operations to join a pharmaceutical manufacturing site. You will lead QA operations, oversee compliance with global regulatory standards, and drive continuous improvement initiatives while collaborating with cross‑functional teams.

Strong leadership and communication skills are essential, with deep knowledge of cGMP, FDA/EMA, and audit processes.

Competenze

  • Experience in QA operations within a pharmaceutical manufacturing context.
  • Strong understanding of cGMP, FDA, EMA and international quality standards.
  • Proven ability to lead audits, inspections and regulatory interactions.

Mansioni

  • Manage quality systems and document control, batch certification, and material release.
  • Ensure compliance with global regulations and internal quality requirements.
  • Lead inspections, audits and regulatory interactions.
  • Oversee Quality Management Systems (QMS) and drive continuous improvement.
  • Review and approve quality documents such as SOPs and validation reports.
  • Mentor and develop team members to support professional growth.
  • Represent the Quality function in leadership meetings and cross‑functional projects.
  • Drive initiatives to reduce release cycle times and improve efficiency.

Conoscenze

Leadership
Communication
Analytical
Regulatory knowledge
Problem solving
Team management

Descrizione del lavoro

R&D Partners in Ireland is seeking a Senior Manager in Quality Assurance Operations to join a pharmaceutical manufacturing site. You will lead QA operations, oversee compliance with global regulatory standards, and drive continuous improvement initiatives while collaborating with cross‑functional teams.

Strong leadership and communication skills are essential, with deep knowledge of cGMP, FDA/EMA, and audit processes.

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