Senior Specialist – Compliance

Our client in the biopharmaceuticals sector is looking for a Senior Specialist – Compliance to support their manufacturing facility in Switzerland.

Responsibilities:

  • You will support compliance activities within the manufacturing organisation
  • Support internal audit programs, client audit programs and host client audits
  • Coordinate client audit responses, ensuring adequacy and appropriate remedial actions
  • You will act as lead or support auditor and manage internal audit schedules
  • Responsible for the execution of health authority inspections, including assisting with preparation of inspections and/or responses to observations
  • You will ensure the site is inspection ready at all times by supporting the inspection readiness workstreams and remediation activities
  • You will support the site management review by obtaining and compiling data for quality system performance and improvements
  • You will ensure quality agreements are current
  • Work with colleagues internally and externally to ensure compliance and corporate policies

Requirements:

  • You will be degree educated and have experience within in a QA cGMP regulated environment
  • Have experience in auditing/inspection programs within regulated operations
  • You will have experience executing and managing Quality Systems
  • You should have additional experience within manufacturing, quality control, or technical operations within a regulated environment
  • You must be fluent in French and English, spoken and written

Please do not hesitate in sending your CV and/or the best contact details for yourself to info@thetechrg.com and our team of skilled consultants would be very happy to contact you with more details.

To apply for this job email your details to info@thetechrg.com.