Manufacturing Validation Specialist

at  Agilent Technologies Inc

JOB DESCRIPTION

Are you a driven individual looking for an exciting and highly motivating job? A job where you will play a key role supporting Agilent’s production of reagents for cancer diagnostic to improve quality of life? Then this role is for you!
You will join a team of 11 academics, which is responsible for providing support to daily operations for biological production on our site in Glostrup. The support-group also ensures that the equipment, cleaning, and production processes are validated and meet ISO and GMP requirements. The support area covers antibody production, buffer preparation, antibody dilution, filling, and packaging.
As a manufacturing validation specialist, we are offering you the opportunity to lead all aspects of the execution of validation activities at the Glostrup manufacturing site. This involves practical work with the production, participation in various types of projects, implementation of equipment and involvement in continuous improvements of the production.

QUALIFICATIONS

• You hold 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 environment
• Troubleshooting and optimization of finished production processes
• Fluent in Danish and English
• LEAN competences

Your personal competences:

• Enjoy working both independently and in teams
• Proactive, positive, and supporting personality eager to learn
• Drive and ability to complete tasks to agreed deadlines
• Structured and quality-minded

We offer:

• A job among highly qualified and committed colleagues in an international growing organization developing and producing diagnostic products.
• We guarantee that you will be exposed to exciting challenges and development opportunities, with a high level of influence.

• Complete documentation utilizing a high level of details within the preparation of validation plans, protocols, and reports for both automated equipment, facilities and cleaning.
• Designs and develop cleaning procedures for new products and manufacturing equipment. Additionally, implementation of cleaning strategies.
• Works cross-functionally to ensure adherence to cleaning program documentation and site initiatives.
• Support the daily operation incl. troubleshooting, NCR and CAPA-handling
• Implement smarter / better / faster production steps and to reduce delivery times and remove bottlenecks