Sterilization Process Validation Expert — Drive GMP Quality

SIRE LIFE SCIENCES; Haarlem; On-site; EUR 65,000 - 85,000; Full time

Job summary

SIRE LIFE SCIENCES is seeking a skilled Validation Specialist to support the validation of sterilization processes in Boxmeer, NL. This project-based role focuses on ensuring filtration and sterilization methods meet strict industry standards and GMP guidelines.

You will investigate and optimize filtration techniques, write validation protocols and reports, and collaborate with cross-functional teams on-site to implement process improvements and ensure quality and compliance throughout the

Qualifications

• Minimum of 5–6 years of experience in the pharmaceutical sector.
• Proven experience in writing protocols, validation reports, and technical documentation.
• Strong knowledge of GMP regulations, sterilization, and filtration processes.
• Solid understanding of the chemistry of aqueous and oily solutions.
• Excellent communication skills in English; familiarity with Dutch is a plus but not required.

Responsibilities

• Investigate existing filtration processes used during sterilization.
• Modify and improve filtration methods to ensure they meet sterilization requirements.
• Write validation protocols, reports, and statements to document findings and procedures.
• Collaborate with cross-functional teams on-site to implement process modifications.
• Ensure all activities comply with GMP guidelines and quality standards.
• Support validation activities from initial assessment through to final implementation.

Skills

Written protocols

GMP knowledge

Technical documentation

Job description

SIRE LIFE SCIENCES is seeking a skilled Validation Specialist to support the validation of sterilization processes in Boxmeer, NL. This project-based role focuses on ensuring filtration and sterilization methods meet strict industry standards and GMP guidelines.

You will investigate and optimize filtration techniques, write validation protocols and reports, and collaborate with cross-functional teams on-site to implement process improvements and ensure quality and compliance throughout the