Responsible Engineer for Equipment Support Incubators, Fridges, deep freezers and chambers

Join our team as a Responsible Engineer, managing essential equipment and ensuring compliance with GMP standards. You'll lead the transition to new models, support technical processes, and collaborate with various operations teams. This role offers career growth within a supportive work environment focused on productivity and teamwork.
 

The role
We are seeking a dedicated and proactive Responsible Engineer to join our team. The ideal candidate will support the daily operations and maintenance of critical equipment, including incubators, chambers, fridges, and deep freezers. The Responsible Engineer will ensure all equipment is operational and compliant with GMP regulations and will be instrumental in transitioning old equipment to new models, assisting with engineering and validation processes, and onboarding new equipment. Additionally, this role involves collaboration with the Glass Washers, IBC Washers, and Autoclave operations team, with occasional on-call duties.
 

Key Responsibilities

• Daily Operations: Manage and maintain the functionality and compliance of incubators, chambers, fridges, and deep freezers, ensuring equipment availability for production needs.
• Technical Support: Lead error identification, troubleshooting, and immediate service repair to minimize downtime and ensure continuous operational flow.
• Equipment Transition: Support the upgrade and transition process from old equipment to new models, including onboarding, engineering, and validation efforts.
• Team Collaboration: Integrate with the Glass Washers, IBC Washers, and Autoclave daily operations team to enhance overall equipment management and facilitate seamless operations.
• On-Call Duties: Provide occasional on-call support to address urgent equipment issues outside of regular working hours.
   

Qualifications

• Experience: 2-4 years of engineering experience, preferably within the pharmaceutical industry.
• Experience with cooling equipment is an advantage
• Education: Bachelor’s or Master’s degree in Chemical Engineering or a relevant technical field.
• Regulatory Knowledge: Familiarity with Good Manufacturing Practices (GMP) and related industry regulations.
• Skills: Strong communication skills, problem-solving capabilities, and leadership in technical support operations.
• Experience with the following systems is an advantage; B medical systems, Thermofisher, Kuhner
   

Additional Requirements
Strong ability to lead and manage error-finding processes.
Excellent problem-solving skills with a focus on innovative solutions for equipment-related challenges.
A proactive approach to ensuring equipment reliability and compliance.

The area
Process Technology is a group of more than 100 employees that includes 5 departments: Automation, Process Engineering, Validation, Engineering Science and CAD services. We provide support to site-wide projects by offering our expertise as Automation, Process and Validation Engineers and we maintain overall responsibility for ensuring smooth daily operation including engineering technical leadership, and engineering technical support for all cell culture, purification, and pharmaceutical processing equipment.

We value collaboration, knowledge sharing and take pride in delivering robust services and solutions to our stakeholders. We communicate openly, are inclusive and support each other every day regardless of individual responsibility.

On a person level our internal department workday is open, friendly, humorous, and relaxed. We create our own workday, and an individual and optimal work-life balance is highly prioritized. We meet with each other in social events and have the possibility to work from home, all dependent on nature of tasks and program.
 

Application
Interested candidates should submit their resume and cover letter, highlighting relevant experience and qualifications.

For inquiries, please contact Manager, Process Engineering, Rob Fleuren, at phone no.: +45 91357167.

We are an equal opportunity employer and welcome applications from all qualified candidates.

Working at FUJIFILM Biotechnologies

We offer a competitive compensation package in a site/company growing rapidly, with many opportunities for individual growth, we also offer access to fitness and an attractive canteen.

FUJIFILM Biotechnologies is an industry-leading Biologics Contract Development and Manufacturing Organization (CDMO) with locations in Hillerød, Denmark, Teesside, UK, RTP, North Carolina and College Station, Texas, USA. We use our skills, dedication, and ambition to enable impact for the world’s most innovative biotech and biopharma companies reimagining healthcare’s potential. We work across the entire lifecycle of our customers’ products