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

Agilent; Denmark; On-site; DKK 420,000 - 540,000; Full time

Benefits offered by this job

Free parking

Canteen

Training & development

Job summary

Agilent Technologies Inc. in Glostrup, Denmark, is seeking a dedicated manufacturing support specialist for the BCP unit.

You will join a team focused on providing support to daily operations for production of buffers and antibody dilutions, ensuring ISO and GMP compliance and validating equipment and processes. The role involves daily operation support, procedure changes, CAPAs, continuous improvement, cross-functional projects with QA, regulatory affairs, R&D, Warehouse, Sourcing and

Qualifications

• MSc in engineering, biology or a related field.
• 2–3 years’ experience in a similar role is preferred.
• Experience with GMP and regulated production environments.
• Experience with troubleshooting and optimization of finished production processes.
• LEAN/CI competences.
• Fluent in Danish and English.

Responsibilities

• Support daily operation including troubleshooting and NCR-handling.
• Handle SOP changes (ECO, ECR) and CAPA’s.
• Optimize and continuously improve processes, equipment, and our quality system.
• Participate in projects with stakeholders across Agilent (production, QA, regulatory, R&D, Warehouse, Sourcing, Logistics).
• Process and test method validations.
• Participate in internal and external audits.

Education

MSc in engineering/biology or related chemistry/biotechnology

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.

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.
• Travel Required: No
• Shift: Day
• Duration: 9-12 Months
• Job Function: Manufacturing

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.