Based at the production site in Bordon/London, UK. The site includes manufacturing, packaging, release and logistics activities. Bordon/London, UK is the European release and launch site for oncology. The manager’s role and responsibilities include:

• Develop and lead several quality systems like self inspection program, auditing, training and validation program
• Coordinate external contract manufacturer and laboratories in regards to audits, QA agreements and documentation flow
• Lead external audits and maintain superior compliance levels
• Support review and release products for the European market
• Cooperate with corporate QA network
• Lead and develop direct reports

Requirements:
• Qualified pharmacists or comparable degree
• Qualification as QP desired
• Relevant experience in the health care industry, in operations, quality assurance or quality control desired
• Experience in i.V. products or oncology a plus
• Interest in process oriented quality assurance and regulatory affairs
• Excellent English language skills
• Highly motivated and self starter with good interpersonal skills
• Excellent priority setting and risk taking
• Hands on mentality

Reporting to: Head Quality Unit

For more information, please contact Laura Jones @ Vane Recruitment 02392 361115.