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Academic - IVD Production Improvements & Automation

Job Description


Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek -- so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com .

Would you like to make a difference in diagnosis of cancer? Are you ready to make a difference for your colleagues and improve production facilities to serve Agilent's costumers? Then you might be the person we are looking for to support our growth in Agilent Manufacturing.

Biochemical Production -- Quality Control (BCP-QC) is part of Finished Production in Agilent, Glostrup. We perform incoming QC of raw materials and QC controls of productions, and we manufacture buffers and antibody dilutions. As a lively production department, we focus to deliver high quality diagnostic products to our customers.

As an Academic in BCP-QC , you will drive continuous improvements and automation projects in collaboration with the Department manager, our 18 lab techs and relevant internal & external stakeholders. You will be a key go-to person in BCP-QC, making our continued growth possible, to the benefit of Agilent's costumers.

Your key responsibilities will include:

- Continuous improvements of our production processes and procedures
- Manage and drive local projects and follow the projects through to implementation and completion
- Implement automations and digitalizations
- Update procedures, manufacturing documentation and test papers
- Implement high quality, high-efficient improvements to benefit workflow and working milieu of our personnel


Qualifications


We are looking for a motivated individual with the following background:

- Master's or PhD Degree in Life Science, Science, Engineering or equivalent
- Experience in Production , Manufacturing and/or R&D within a Pharma or Medical Device Regulated Environment
- Experience with lean or continuous improvements (CI)
- Experience with implementation of automations
- Knowledge of GMP (Good Manufacturing Practices) is an advantage
- An experience with procedure update/change control is a plus
- Full fluency in both Danish and English

As a person, you are outgoing with a genuine interest in making a difference and add value . You thrive in a regulated GMP environment and you are not afraid of taking initiatives . You are efficient when it comes to updating procedures and processes to implement improvements.

In addition, collaboration is key in this position. You also have great communications skills to interact with technicians, lab techs, other academics including QA and R&D. We appreciate humor and interacting with a smile.

We offer
- An opportunity to make a difference
- An independent job in an open- and knowledge sharing atmosphere
- Collaboration with skilled and engaged colleagues based upon our values trust, respect, teamwork and uncompromised integrity
- Room for innovation and contribution
- Commitment to work/life balance and an opportunity to grow within a world-class company

Questions
If you have any questions about this position, please contact recruiter César Lecomte (cesar.lecomte@non.agilent.com) or department manager Line Thomsen (line.thomsen@agilent.com)

Agilent technologies inc. is an equal opportunity employer and value diversity at our company. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, disability status or any other protected categories under all applicable laws.



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