Utility engineer

Job title:

Utility engineer

Company:

Novo Nordisk

Job description

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Accept ClosePress Tab to Move to Skip to Content LinkSearch by KeywordSearch by LocationLoading…Category×Select how often (in days) to receive an alert:×Select how often (in days) to receive an alert:Utility engineerCategory: Engineering & TechnicalLocation:Måløv, Capital Region of Denmark, DKAre you looking for a new challenge where you can apply your extensive knowledge within facilities, equipment and qualification? 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?If so, read on to find out more about our Utility Engineer opportunity in Clinical Supply Packaging & Shipping (CSPS) at Site Måløv.About the positionAs 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 performanceDrive LEAN processes for systematic problem-solving and execute project management activitiesImplement new equipment/facilities to support the growth in clinical trialsAs 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.QualificationsTo be successful in this position, you hold a Bachelor, Master or PhD in etc. Biotechnology, Design or Process. 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 PlannerGMP-knowhow / change control / deviation handlingManagement of GxP facilities including troubleshooting, optimisation and handling of critical alarmsValidation of GxP facilities including HVAC, BMS and FMSProject management with technical knowledgeStakeholder management cross functionally and with external suppliersAs 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.About the departmentThe 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 Novo NordiskAt Novo Nordisk, 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.ContactFor further information about the position, please contact Associate Manager Daniel Bøjle +45 3075 6934.Deadline28 April 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 Novo Nordisk 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.

Expected salary

Location

Hovedstaden

Job date

Tue, 16 Apr 2024 23:11:26 GMT

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