Academic for production support and process optimization (1 year position)

DK05 DAKO Denmark R&D & Manufacturing; Glostrup Kommune; On-site; DKK 550,000 - 850,000; Full time

Benefits offered by this job

Excellent canteen

Free parking

Training and development

Work-life balance

Job summary

Agilent Technologies Inc. in Glostrup, Denmark, invites you to join a busy BCP production team responsible for buffers and antibody dilutions under ISO and GMP requirements.

You will support daily operations, troubleshoot issues, and help validate equipment and processes. The role involves implementing ECO/ECR changes, CAPAs, SOP updates, and continuous improvements across processes, equipment and our quality system.

Qualifications

• MSc in engineering, biology or related chemistry/biotech field.
• 2–3 years of experience in a similar GMP-regulated role.
• Experience with GMP and regulated production environments.
• LEAN/CI competencies.

Responsibilities

• Support daily operation, troubleshoot, and handle NCRs.
• Manage SOP changes (ECO/ECR) and CAPAs.
• Improve processes, equipment and quality system.
• Collaborate with QA, regulatory affairs, R&D, warehouse, sourcing and logistics.
• Participate in audits and process/test validations.

Skills

LEAN/CI competences

Fluent in Danish & English

Education

Masters degree in engineering/biology or related chemistry/biotech field

Job description

Job Description

Job Description BCP is a part of Agilent's Finished Production in Glostrup and is organized in three teams - two production teams and one support team. You will join a team of 2 academics, which is responsible for providing support to daily operations for our production of buffers and antibody dilutions. As a busy production department, we focus on delivering high-quality products to our customers in compliance with ISO and GMP requirements. The support team also ensures that the equipment and production processes are validated. We offer a challenging job with a high level of influence. Your primary responsibility will be: support of the daily operation incl. troubleshooting and NCR-handling. Handling procedure (SOP) changes (ECO, ECR) and CAPA’s. Optimization and continuous improvements on processes, equipment, and our quality system. Participation in projects with different stakeholders in Agilent, working closely together with the production areas, QA, regulatory affairs, R&D, Warehouse, Sourcing and Logistics. Process and test method validations. Participation in both internal and external audits.

Qualifications

• Professional qualifications: You hold an MSc in engineering, biology or similar education within chemistry or biotechnology. Preferably 2-3 years' experience from a similar position. Experience with GMP and regulated production environments. Experience with troubleshooting and optimization of finished production processes. LEAN/CI competences.
• Fluent in Danish and English.

Personal qualifications

A driven and helpful individual with a genuine interest in making a difference for colleagues and stakeholders. Enjoy working both independently and in teams. Structured and quality-minded and driven to execute tasks within deadlines. Has a proactive and positive mindset, with a curiosity to learn and develop in a dynamic setting where humor and a smile are much appreciated in daily interactions.

We offer

• An exciting job among highly qualified and committed colleagues in an internationally growing organization.
• We guarantee that you will be exposed to exciting challenges and development opportunities, with a high level of influence.
• A vibrant environment among highly qualified colleagues, with a supportive attitude who will make sure that you get all the training and assistance you need to succeed in the role.
• An excellent canteen and free parking.
• Optimal conditions for a good work/life balance.

Questions

For further information about the position please contact Department Manager Maria Stine Enghoff on [e-mail] or on [phone].

Additional Details

This job has a full time weekly schedule.

Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.

Travel Required: No. Shift: Day. Duration: 9-12 Months.

Job Function: Manufacturing Graduate and Student.

About Agilent

As a global leader in laboratory and clinical technologies, we are passionate about bringing great science to life. Our commitment to quality and innovation supports cutting-edge life science research, patient diagnostics, and ensures the safety of water, food, and pharmaceuticals. As scientists and clinicians pursue small, everyday advances and life-changing discoveries, we provide trusted answers to their most critical questions and challenges. Leveraging more than 50 years of expertise, we create advanced instruments, software, and consumables supported by teams of highly skilled and knowledgeable people. With 18,000 employees around the world, our global reach and comprehensive solutions provide the most reliable and accurate results, as well as optimal scientific, economic, and operational outcomes. We work collaboratively with our customers on their journey to make a real difference in human lives. Our culture is founded on trust, respect, and uncompromising integrity, and we pride ourselves on being a dynamic and inclusive workplace that celebrates diversity and fosters innovation. We can't wait for you to join us as we continue our mission to improve the world around us.

Information about Agilent is available at Agilent.com.