
Adept Validation Specialist
2 weeks ago
We are seeking a highly skilled professional to lead and support quality control for equipment qualification, oversee IQ, OQ, PQ activities, and mentor junior staff in best practices.
">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.
- Ensure proper planning of materials and consumables.
- Maintain documentation quality and regulatory compliance.
- Coordinate with vendors and contractors to ensure standards are met.
The ideal candidate will have experience, leadership skills, and a strong understanding of regulatory and industry best practices.
">Requirements:- Bachelor's or Master's degree 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.
- Competitive salary.
- Relocation package including travel support, temporary housing, and financial assistance.
- Private health insurance and life cover.
- 22 days annual leave plus 10 public holidays.
- Paid overtime or compensatory time.
- Company phone or reimbursement.
- Pension contributions and support for professional memberships.
- Ongoing training and development opportunities.
Why Work with Us?
">- You'll work in a supportive and collaborative environment on innovative life sciences projects across Europe.
- We're committed to your growth through hands-on experience, certification support, and career development in a dynamic, international setting.
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