Job Description:
As a Senior Validation Engineer, you will be responsible for ensuring the highest quality standards during equipment qualification processes and providing technical guidance across validation activities.
Key Responsibilities:
* Lead and support quality control for equipment qualification
* Oversee IQ, OQ, PQ activities and documentation
* Mentor junior staff and promote best practices
* Review and complete validation protocols (TOPs, QSRs)
* Ensure proper planning of materials and consumables
* Maintain documentation quality and regulatory compliance
* Coordinate with vendors and contractors to ensure standards are met
* Participate in FAT, SAT, and other qualification phases
* Drive continuous improvement in validation procedures
Requirements:
* Bachelor's or Master's in Science, Engineering, or related field
* Minimum 5 years of experience in validation, QC, or commissioning in pharma/biotech
* Advanced English proficiency (C1 Cambridge level or higher)
* Strong written and verbal communication skills
* Solid understanding of GMP and relevant regulatory frameworks
* Experience with aseptic fill/finish, OSD, gene therapy, or biotech processes
* Willingness and ability to relocate
What We Offer:
* Competitive salary
* Relocation package: travel support, temporary housing, and financial assistance
* Private health insurance and life cover
* 22 days annual leave plus 10 public holidays
* Paid overtime or comp time
* Company phone or reimbursement
* Pension contributions and support for professional memberships
* Ongoing training and development opportunities
Why This Role?
You'll work in a supportive and collaborative environment on innovative life sciences projects across Europe. This is an ideal opportunity for experienced engineers seeking career progression in an international environment.