Company
A leading pharmaceutical manufacturing company dedicated to producing sterile medicines. The organization specializes in mixing antigens and oils in large vessels and is committed to maintaining the highest standards of quality and safety throughout its production processes.
Job Description
We are seeking a Senior Validation Specialist to support a key project focused on validating and improving sterilization processes. The successful candidate will play a crucial role in investigating filtration methods to ensure they meet stringent sterilization requirements, ultimately enhancing the safety and efficacy of the products.
Responsibilities
- Investigate existing filtration processes to identify issues with current filtration efficiency.
- Modify and optimize the filtration procedures to meet sterilization standards.
- Write detailed protocols, statements, and validation reports in compliance with GMP requirements.
- Collaborate with multidisciplinary teams on-site to execute validation activities.
- Ensure all documentation and processes align with industry and internal quality standards.
- Contribute to the ongoing improvement of sterilization validation projects.
Requirements
- Minimum of 5–6 years’ experience in the pharmaceutical or biotech sector, particularly in validation or sterilization processes.
- Proven ability to write protocols, validation statements, and technical reports.
- Strong knowledge of GMP, as well as the chemistry of aqueous and oily solutions.
- In-depth understanding of filtration processes used in sterile production.
- Fluent in English; proficiency in Dutch is a plus but not required.
Other Information
If you are interested and want to apply, please submit your application via the apply button below and contact me.
58436
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Jyothi Shiva
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