Specific activities and responsibilities

  • Collaboration with Head of Quality and Process Improvement to support ongoing development, implementation and maintenance of the corporate quality system.
  • Develop and maintain the ProductLife Group quality management system, including requirement for obtaining ISO 9001 certification, with ongoing alignment with the corporate quality management system
  • Recommend, develop and maintain the controlled document system, including SOPs, WPDs and any associated forms and templates.
  • Ensure data in Quality trackers / system are accurate, up to date and entered in a timely manner, to enable automated reporting.
  • Identify process efficiency/effectiveness issues and provide solutions for improvement.
  • Maintain a strong working knowledge of SOPs as well as ICH, GCP, local regulations and guidelines.
  • Provide quality verification and oversight including corrective action plans for activities not meeting quality standards.
  • Provide interpretation and relay to the Managers the need for continuous improvement of processes.
  • Management and implementation of ProductLife Group annual risk based audit program (occasional travel)
  • Management of internal and client audit and inspection findings.
  • Act as the key point of contact for client auditors and vendors PLG audits.
  • Support and maintain quality activities for oversight of vendors, suppliers and subcontractors to ensure they are functioning appropriately and audit as required.
  • Oversee, maintain and improve training programs within ProductLife Group.
  • Work with the departments to develop guidelines and metrics to assure quality and compliant deliverables.
  • Quality representative at Global Quality Management Team meetings (occasional travel).
  • Collaborate effectively with other managers.

Required education

Bachelor’s or higher graduate degree in a science related field, or equivalent experience

Required experience

8 + years’ experience within a Quality role in Pharmaceutical industry + previous role or knowledge in PV domain.

Additional experience and/or skills

Client relationship Autonomy proactivty

Publish Date

18 August, 2026

Spontaneous Application

QPI Expert (Quality + Pharmacovigilance) - VAF 636

New opportunities open up across PLG all the time. If nothing matches right now, send us a spontaneous application: we will keep you in mind for what comes next.

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