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Process Engineer with a passion for automatisation

Do you have a passion for automation in biopharma manufacturing? Do you want to be part of a company helping customers bring new advanced biological products to market? And would you like to work at our multiproduct facility in Copenhagen? Then join a dynamic and international company where everyone is responsible for delivering right on time as one team!

The JobAGC Biologics is an international and modern organization with production sites in Europe, Japan and US and are one of the largest contract development and manufacturing organization (CDMO) in the world. Currently, AGC Biologics employs approx. 1000 people worldwide, 550 situated in Denmark close to Copenhagen.

The manufacturing department consists of five manufacturing lines, running both early and late stage clinical and commercial manufacturing at 500L – 12.000L scale, covering both microbial fermentation, mammalian cultivations and downstream operations.

 

As a Process Automation Engineer, you will be part of one of our manufacturing teams working together with skilled colleagues in a key position that covers upstream and downstream manufacturing equipment and automation systems.

The Process Automation Engineer reports to the manager of the team with a dotted line reporting to the Vice President of Technical Operations. In this position, you will work at all levels of the organization and across departments.You will be supporting development and integration of new IT systems in the manufacturing environments and commissioning, facilitate test and qualification of these systems. In addition to this, you will be the manufacturing automation system administrator. We expect you to be active in the participation in the team projects, and be responsible for planning, estimation and coordination of tasks in generel. 

Your responsibilities are furthermore: 

  • Equipment/facility fit and gap assessments for new product introductions, identifying and leading equipment and system purchase, upgrade or rebuild projects
  • Build business cases for investment applications
  • Stay current on newest biologics manufacturing technologies
  • Lead training initiatives related to new technologies, equipment or systems
  • Support manufacturing in investigations related to equipment or system issues
  • Secure compliant and robust equipment and system onboarding and implementation

What you need to be successful in the posted position 

 We are looking for a Master or Bachelor degree within Science e.g. chemical engineer, biotech engineer, computer science, physics or similar. We also expect you to have several years of experience within GMP manufacturing from a manufacturing or engineering team. It is important that you have a good understanding and interest in Manufacturing automation systems and a basic knowledge on IT infrastructure.

We need you to be:

  • Experienced with data visualisation tools and data ingestion from various manufacturing systems
  • Experienced within Lean or operational excellence.
  • Comfortable in English (orally as well as in writing).
  • Experienced in Project management.

We are looking for a person that excels in execution and takes pride in efficient completion of tasks and projects at hand. The right person works well in a matrix organization and is an adept communicator who can create results at all levels of the organization.

Application

We cooperate with Adecco on recruitments. Accordingly Adecco will be responsible for the recruitment process. For more information about the position, please contact Adecco's recruitment team.

 

We continuously evaluate incoming applications and conduct interviews accordingly. Therefore, please submit your application and CV as soon as possible. When the right candidates are found, the ad will close.

 NB. Start date will latest be December, 1st 2020.

About AGC BiologicsAGC Biologics (AGC) is a global Contract Manufacturing Organization (CMO) with biomanufacturing facilities in Europe, Japan and the USA. The company provides a comprehensive range of commercial and clinical cGMP biologics manufacturing services, from DNA to active pharmaceutical ingredient (API). The company’s team and approach are tailored to each of its client’s needs, whether turnkey manufacturing or sophisticated, stand-alone analytical, formulation and stability services.

AGC Biologics also offers non-exclusive license to CHEF1™, a proprietary CHO cell line development platform. CHEF1 delivers stable, high-titer, production-quality cell lines in optimized time frames. It is the foundation of CMC Biologics’ innovative approach to cell line and process development.

Visit www.agcbio.com to learn why AGC Biologics is a World Leader in process development and contract manufacturing. 


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