Utility Engineer for clinical trials
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Måløv
Do you want to combine your extensive knowledge within utility with stategic planning and project management? Do you have a strong passion for managing and validating GxP equipment/systems in a setup that support the growth of the business and ensure the patient safety? And do you want to be part of a growing Clinical Supply Packaging & Shipping (CSPS) where we secure all Novo Nordisk products for clinical trials are packed and delivered to patients all over the world? Then apply for this exiting postion as Utility Engineer in Clinical Supply Packaging & Shipping (CSPS) at Site Måløv. About the position As Utility Engineer you will be responsible for the current and future equipment/facilities, including HVAC, BMS, and FMS. Your responsibilities will include: Oversee upgrades, rebuilds, and problem-solving initiatives to maintain equipment in a validated state and enhance performance
Drive LEAN processes for systematic problem-solving and execute project management activities
Work with strategic planning and implement new equipment/facilities to support the growth in clinical trials
As the Utility Engineer, you will work closely with various internal and external stakeholders, including project teams, regulatory bodies, vendors, and other departments. Your role will be pivotal in ensuring seamless collaboration to achieve our departmental and organizational goals. Your attention to detail and commitment to high-quality solutions will be instrumental in presenting solid validation activities, change requests, deviations, and documentation in audit situations. Qualifications You hold a Bachelor or Master in etc. Biotechnology, Design, Process og similar. Hands-on experience within equipment and validation is a plus. Ideally you join the team with minimum 3 year’s experience and a background within GxP regulated environment in the pharmaceutical industry. But other regulated industries like aero/space, electronics, plastic production and similar is also durable. The following experiences will be a plus: Microsoft Office, Teams and Planner
GMP-knowhow / change control / deviation handling
Management of GxP facilities including troubleshooting, optimisation and handling of critical alarms
Validation of GxP facilities including HVAC, BMS and FMS
Project management with technical knowledge
Stakeholder management cross functionally and with external suppliers
As a professional, you are self-motivated, thrive working independently and enjoy driving projects, improvements, and initiatives across an organisation. You have a structured approach towards challenges and utilise your problem-solving skills to create a standardised way of working. Furthermore, you have a visionary and innovative outlook to drive process optimisation and digitalisation. Also, you are passionate about the automation and packing machinery industry with a knowledge and interest in future products and solutions. You are fluent in English and prefeable fluent in Danish also. About the department The CMC Clinical Supplies Packaging & Shipping (CSPS) department is in Måløv and currently consists of 110 employees divided into six teams. Our overall goal in CMC Clinical Supplies is to ensure timely supply of our clinical studies to patients. We are responsible for packaging and distributing products for clinical studies and we work closely with the rest of the Clinical Supply Chain at CMC to achieve our ambitious goal of delivering high quality products on time to patients worldwide. We continuously work to optimize our processes, reduce lead time and efficient use of resources using various LEAN tools. Working at At , we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact For further information about the position, please contact Associate Manager Daniel Bøjle +. Deadline 31 October 2024, but please apply as soon as possible as interviews will take place on an ongoing basis. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. Also, please refrain from adding a photo to your CV to ensure an efficient and fair recruitment process. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Måløv.
Jobbet er oprettet på vores service den 12.6.2024, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Øvrige
- Måløv
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