We are seeking an experience SIP Validation Contractor to join our client for a 6 month project in Finland. The SIP Validation Contractor will be responsible for validating sterilization-in-place (SIP) processes and protocols for their sterile ophthalmics production. The ideal candidate will have extensive experience in SIP validation, using eLab equipment, and conducting process qualifications. This role requires a self-starter with a minimum of 5 years of relevant experience who can quickly integrate into our team and drive validation activities forward.
Key Responsibilities:
- Develop, execute, and review SIP validation protocols and reports.
- Ensure compliance with regulatory standards and company policies throughout the validation process.
- Conduct process qualifications, including performance qualification (PQ) and operational qualification (OQ).
- Collaborate with cross-functional teams to address validation-related issues and ensure timely project completion.
- Utilize eLab equipment effectively for validation activities and data collection.
- Provide expertise and support for continuous improvement initiatives related to SIP processes.
Qualifications:
- Bachelor’s degree in Life Sciences, Engineering, or a related field.
- 5+ years of experience in SIP validation within a sterile pharmaceutical or ophthalmic environment is a plus
- Strong knowledge of validation protocols and regulatory requirements (e.g., FDA, EMA).
- Proficiency in using eLab equipment and validation software.
- Equipment validation experience
EU (Onsite): SIP Validation Contractor (236022)