Your new company

Legend Biotech is a global biotechnology company dedicated to developing, manufacturing, and commercializing innovative and life-saving cell therapies for the treatment of chronic and life-threatening diseases, such as cancer.

Your new role

• Develop and execute sterilization and decontamination cycle validation strategies in alignment with product requirements.
• Lead/support the design of business cases, study designs, and project implementations.
• Act as a Subject Matter Expert (SME) for sterilization and decontamination processes.
• Ensure seamless knowledge transfer across functions within MSAT and other relevant teams.
• Perform data trend analysis and evaluate process performance, including validation study assessments.
• Provide scientific and cGMP expertise to support process lifecycle activities and ensure compliance with regulatory requirements.
• Lead and support large-scale projects focused on process optimization and operational excellence.
• Participate in regulatory inspections and contribute to compliance-related documentation such as Change Controls, CAPAs, and risk assessments.

Your profile

• 5–10 years of relevant experience in a cGMP environment within the pharmaceutical industry.
• Strong background in sterilization/decontamination validation and manufacturing support.

• Fluent in English (knowledge of Dutch is a plus).

• Ability to work independently with minimal guidance.
• Strong organizational skills, capable of managing multiple priorities in a fast-paced environment.
• Excellent communication and presentation skills.
• Ability to synthesize complex technical issues and communicate effectively at all organizational levels.
• Strong problem-solving, analytical, and critical-thinking skills.
• Team-oriented mindset with the ability to build strong cross-functional partnerships.
• A results-driven approach with a commitment to continuous improvement.

• In-depth knowledge of cGMP regulations related to sterilization and decontamination processes.
• Experience in conducting root cause analysis and implementing corrective and preventive actions.
• Strong statistical analysis skills for data-driven decision-making.
• Familiarity with regulatory submission processes and requirements for manufacturing validation.

What you'll get in return

• A meaningful job with an excellent work-life balance.
• A supportive and innovative work environment.
  We value and encourage learning and personal development.
• The opportunity to work with people from all over the world.
• A contract of indefinite duration and an attractive salary package complemented by many fringe benefits, such as additional statutory vacations, meal vouchers, group and hospitalization insurance, double vacation pay, an end-of-year and performance bonus.
• Many fun and informal events.

What you need to do now

Are you interested in this role? Please click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.