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.