Quality Management System (QMS) Manager

Quality Management System (QMS) Manager

Your new company

For our client, a global manufacturing pharmaceutical company, we are looking for a senior Quality Management System (QMS) Manager, responsible for a team accountable for the implementation, maintenance and monitoring of the Corporate Quality Management System (QMS) at site level. The mission is related to the compliance of the process related to the site QMS to Corporate Guidelines, GMP and applicable international standards.

Your new role

  • Responsible quality representative, main point of contact for quality topics related to the site QMS
  • Owner and responsible for GxP Training management, Documentation management, quality related Master Data Management at site level
  • Local owner of electronic Quality Management Tools such as, but not limited to, Quality Forward and eDMS
  • Own, plan and prepare for Local Quality Forum
  • Assure QMS-related operations are executed in compliance with GxP, internal procedures, guidelines providing expertise and support the resolution of issues
  • Lead the QMS Team promoting a quality culture in line with the group's values
  • Work with different stakeholders to ensure business needs are met in a compliant manner
  • Review and approve risk assessments, change controls, deviations, their investigations and associated CAPAs
  • Edit, review, approve GMP documents and internal procedures
  • Support internal, external, customer audits and assist during Health Authority Inspections as required
  • Adheres to the principles communicated within the ESMS Policy of the company for the purpose of observing the rules of the Health & Safety at Work and the Environmental & Safety Management System

What you'll need to succeed

  • University degree in Pharmacy, Chemistry, Biology, or relevant Life Science
  • Minimum of 5 years of relevant experience in Quality Assurance within the pharmaceutical industry, with at least 2 years in a managerial position
  • Proven cross-functional project management skills
  • Strong knowledge of GMP processes and regulations, pharmaceutical quality assurance principles and regulatory requirements
  • Excellent analytical problem-solving skills
  • Leadership and team management capabilities
  • Flexibility and ability to manage competing priorities
  • Effective communication and negotiation skills
  • Collaborative, team-spirited, positive, and energetic person
  • English advanced

What you'll get in return

  • Developing your career in a prestigious multinational Life Sciences company
  • Promoting and developing various projects for a top portfolio of products
  • Competitive salary package

What you need to do now


If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.


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Sumar

Tipul locului de muncă
Permanent
Industrie
Produse farmaceutice
Oraș
Bucharest
Domeniu
Life Sciences
Referinţă
1194562
Data de incetare
31 Aug 2025

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