Senior Pharmacy Quality Lead - GMP/GDP Expert

Alliance Healthcare Management Services Limited

Alkmaar

Vor Ort

EUR 90.000 - 130.000

Vollzeit

14 Tage+

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Zusammenfassung

Cencora is seeking a qualified quality leader to ensure pharmaceutical quality, regulatory compliance, and continuous improvement across the organization.

You will develop and maintain the QMS, lead audits, approve validation and CAPA activities, and mentor quality teams while collaborating with regulators and partners.

A Master’s in Pharmacy and 3+ years in a regulated pharmaceutical environment are required, with strong English communication and stakeholder management.

Qualifikationen

  • Master's Degree in Pharmacy and valid registration (e.g., BIG).
  • At least 3 years in a regulated pharmaceutical environment.
  • Strong knowledge of GDP and GMP guidelines.
  • Experience with QMS and regulatory frameworks.
  • Experience auditing and regulatory inspections.
  • Proven leadership and people management skills.
  • Experience in process improvement and optimization.
  • Excellent communication and stakeholder management.
  • Fluency in English, written and spoken.

Aufgaben

  • Oversee quality management systems and regulatory compliance.
  • Ensure compliance with laws, regulations, and GDP/GMP standards.
  • Lead audits and liaise with regulatory bodies.
  • Authorize release and control of packaging processes and validated equipment.
  • Coach and develop quality teams; foster continuous improvement.
  • Act as primary contact for quality-related issues and recalls.
  • Stop production if quality risks are present.

Kenntnisse

Quality leadership
Regulatory knowledge
QMS experience
Audits experience
CAPA & recalls
Validation experience
Stakeholder management
Analytical thinking
English proficiency

Ausbildung

Master's in Pharmacy

Jobbeschreibung

Cencora is seeking a qualified quality leader to ensure pharmaceutical quality, regulatory compliance, and continuous improvement across the organization.

You will develop and maintain the QMS, lead audits, approve validation and CAPA activities, and mentor quality teams while collaborating with regulators and partners.

A Master’s in Pharmacy and 3+ years in a regulated pharmaceutical environment are required, with strong English communication and stakeholder management.

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