Continuous Improvement Lead, Plant Engineering

Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market.

Do you enjoy driving the continuous improvements, solving complex technical challenges, and developing digital tools in a purpose-driven environment? Then this might be the perfect opportunity for you!

The Department & Team:

You will be joining the Compliance team, part of Plant Engineering department, which falls under the broader Engineering division. Plant Engineering is responsible for manufacturing maintenance of production assets, metrology, utility operations, and asset management. With a strong service mindset, Plant Engineering delivers reliable and professional support across the entire Copenhagen site. The Compliance Team is key in driving Deviation, Change Control and CAPA records, maintain procedures owned by the department coordinate and follow-up on external audits and authority inspections. The ambition is that the team will also take responsibility for driving quality improvements projects within Plant Engineering department and here you will play the crucial role to achieve this ambition.

The Role:

You will be responsible for analyzing data connected to Plant Engineering identifying improvement opportunities across the organization. You will lead the optimization of workflows, develop, and operate digital solutions such as data dashboards, process automation and equipment data analysis.

Primary responsibilities will include:

Identify, define, and lead continuous improvement initiatives by using LEAN tools and methods.

Analyze complex data and propose improvement potentials.

Support with facilitation of systematic problem solving in the complex technical issues.

Design and maintain digital tools (low code/no code tools) to monitor area performance.

Lead digitalization improvements projects (e.g., automatization of review processes by applying RPA).

Support with facilitation of systematic problem solving in the complex technical issues.

Your Profile:

We are looking for a certified and experienced LEAN profile with the capability of developing digital tools in low code/no code systems as MS Power Platforms, Grafana and similar. You can quickly adapt to new situations in a changing environment, and you are curious to know the processes and you love to interact with colleagues across the organization. You also have the following qualifications:

Relevant academic background within e.g., IT/OT, engineering, industrial management, supply chain management, or equivalent.

Competences within Power Query M, SQL, data tracking and understanding of API-integrations

Experience with Robotic Process Automation (RPA) or similar

Knowledge of data engineering and data modelling

Structured approach to planning and execution of your tasks

Your Application:

To apply, please submit your CV. We encourage you to apply, even if you do not meet every requirement. If you need further information about the position, please feel free to contact Katarzyna Holmbjerg, Manager of Plant Engineering Compliance team by mail: . If we see a potential match, one of our recruiters will contact you to discuss your application. Please note, the hiring process for this position will begin in Week 32.

Our culture at AGC Biologics is defined by the six core values: Knowledge, Trust, Quality, Ingenuity, Accountability and Teamwork. Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe.

AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit Want to keep posted about our growth and learn more about our company? Follow us on LinkedIn and give us a quick Like on Facebook!

AGC Biologics offers a highly competitive compensation package and a friendly, collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances.

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