Company Overview

Our client is a global consulting firm specialising in quality solutions for the life sciences industry. Their services span compliance, validation, and regulatory support, helping pharmaceutical and biotech companies meet international standards. With a strong presence worldwide, they deliver tailored strategies to ensure operational excellence and regulatory success.

The Role

We are seeking consultants to join a major validation project in Nantong, China. This is a full-time, on-site freelance position for an initial 1-year contract, with the possibility of renewal. The role is critical to ensuring compliance with global GMP standards and supporting the successful execution of complex validation activities.

Key Responsibilities

• Develop and oversee the Project Validation Master Plan

• Review and ensure the quality of all validation deliverables

• Supervise execution of validation activities, ensuring compliance with GMP regulations (US/EU/CN)

• Conduct gap analysis and implement improvements to validation systems

• Train and mentor validation staff; support governance of validation projects

Qualifications

• 15+ years of experience in validation management, with expertise across all CQV areas

• Degree in Biotechnology, Bioengineering, Pharmaceutical Sciences, or a related field

• Proven track record in projects approved by FDA or EMA

• Experience in multinational biopharmaceutical companies

• Strong knowledge of GMP regulations (China, US, EU)

• Ability to draft technical documents in Chinese and English; English fluency required

The Offer

• Location: Nantong, China (Full-time, on-site)

• Contract: Freelance, 1-year (renewal possible)

• Salary: 300,000 - 450,000 RMB per year

• Opportunity to work on high-impact projects with global regulatory significance

• High-priority role with potential for extended engagement

Send over your CV and a summary below to discuss further.