Manufacturing Validation Professional
1 week ago
We are seeking a skilled Manufacturing Validation Professional to join our team at Agilent Technologies, Inc. in Glostrup, Denmark.
Job DescriptionThis is a full-time position with a weekly schedule. The successful candidate will play a key role in supporting daily operations for biological production on our site. Key responsibilities include leading all aspects of validation activities, implementing equipment qualification, and ensuring adherence to cleaning program documentation.
The ideal candidate will have experience managing GMP and regulated production environments, troubleshooting and optimizing finished production processes, and working cross-functionally with teams. Fluency in Danish and English is required.
Key Responsibilities:- Develop and implement validation plans, protocols, and reports for automated equipment, facilities, and cleaning.
- Design and develop cleaning procedures for new products and manufacturing equipment.
- Support daily operations, including troubleshooting, NCR, and CAPA-handling.
- Implement smarter/better/faster production steps to reduce delivery times and remove bottlenecks.
To be successful in this role, you will need:
- A MSc in engineering, biology, or similar education within chemistry or biotechnology.
- Preferred knowledge within cleaning and cleaning validation.
- Experience managing GMP and regulated production environments.
- Troubleshooting and optimization of finished production processes.
- Fluency in Danish and English.
We offer a competitive salary range of $85,000 - $115,000 per year, depending on location and experience. Additionally, we provide a comprehensive benefits package, including health insurance, retirement plan, and paid time off.
About Agilent Technologies, Inc.Agilent Technologies, Inc. is an equal opportunity employer. We are committed to diversity and inclusion in the workplace. If you are passionate about quality assurance and validation, we encourage you to apply for this exciting opportunity.
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