Machine Safety Lead
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Do you have solid experience within machine safety, risk assessment and CE labelling and do you have knowledge within the machinery directive? Then we might have the right position for you as our new Mechanical Engineer in Novo Nordisk Pharmatech A/S, read more and apply now!
The position
You will be a part of Novo Nordisk Pharmatech A/S who produces important ingredients to the pharmaceutical production and will be the overall responsible for CE labelling of the new facility including equipment. Among your responsibilities, you will:
• facilitate risk assessment together with advisors and suppliers to ensure that all equipment meets the requirements of the machine directive
• ensure that all documentation, data, drawings, and maintenance instructions meet the applicable requirements and guidelines
• be responsible for anchoring all aspects of CE labelling and Novo Nordisk Pharmatech A/S systems
In this role you will be part of a brand-new greenfield project, work with new technology and have the chance to help build a new facility from scratch, becoming responsible of the safety of equipment and utilities in a newly established site. Qualifications To succeed in this role, we imagine that you have:
• a master’s degree in Engineering, Technology Management and Marine Engineering or similar
• experience with CE labelling
• experience with risk assessment of equipment in the production industry
• knowledge within the machinery directive, pressure equipment directive and other relevant directives
• full English proficiency, and Danish knowledge will be seen as an advantage In general, you have a good technical insight and a natural talent for IT, combined with project planning skills and the ability to ensure that advisors and suppliers meet our requirements.
About the department
You will become part of a newly established project organisation aimed at handling the increased demand from Novo Nordisk A/S, by establishing a new facility. You will also be affiliated with the Technical Support department, where you will be able to draw on the experiences of employees and people managers within your field. About Novo Nordisk Pharmatech A/S
Novo Nordisk Pharmatech A/S is a 100% owned subsidiary of Novo Nordisk located in Køge. We are more than 300 people covering the entire value chain from R&D and Business Development to Manufacturing, Marketing and Sales. Novo Nordisk Pharmatech A/S is a global and leading manufacturer of pharmaceutical ingredients for the pharmaceutical and biopharmaceutical industries. Our purpose is to enable better medicines by providing sustainable pharmaceutical materials through innovative and customized solutions. Our product range consists of Quaternary ammonium compounds (Quats), Recombinant Insulin, Customized Purification Resins, and Specialty Enzymes.
Contact
For further information about the position please contact Senior Manager Jan Karkov Carstensen on mobile number +45 31 99 59 11.
Deadline
21 May 2023
Applications will be evaluated continuously, and candidates may be called for an interview before the deadline, so please apply as soon as you can. You do not need to attach a cover letter to your application, but please include a few lines about your motivation in your resume or CV. Additionally, please avoid the use of photos in your CV. This provides a better and more fair 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.
The position
You will be a part of Novo Nordisk Pharmatech A/S who produces important ingredients to the pharmaceutical production and will be the overall responsible for CE labelling of the new facility including equipment. Among your responsibilities, you will:
• facilitate risk assessment together with advisors and suppliers to ensure that all equipment meets the requirements of the machine directive
• ensure that all documentation, data, drawings, and maintenance instructions meet the applicable requirements and guidelines
• be responsible for anchoring all aspects of CE labelling and Novo Nordisk Pharmatech A/S systems
In this role you will be part of a brand-new greenfield project, work with new technology and have the chance to help build a new facility from scratch, becoming responsible of the safety of equipment and utilities in a newly established site. Qualifications To succeed in this role, we imagine that you have:
• a master’s degree in Engineering, Technology Management and Marine Engineering or similar
• experience with CE labelling
• experience with risk assessment of equipment in the production industry
• knowledge within the machinery directive, pressure equipment directive and other relevant directives
• full English proficiency, and Danish knowledge will be seen as an advantage In general, you have a good technical insight and a natural talent for IT, combined with project planning skills and the ability to ensure that advisors and suppliers meet our requirements.
About the department
You will become part of a newly established project organisation aimed at handling the increased demand from Novo Nordisk A/S, by establishing a new facility. You will also be affiliated with the Technical Support department, where you will be able to draw on the experiences of employees and people managers within your field. About Novo Nordisk Pharmatech A/S
Novo Nordisk Pharmatech A/S is a 100% owned subsidiary of Novo Nordisk located in Køge. We are more than 300 people covering the entire value chain from R&D and Business Development to Manufacturing, Marketing and Sales. Novo Nordisk Pharmatech A/S is a global and leading manufacturer of pharmaceutical ingredients for the pharmaceutical and biopharmaceutical industries. Our purpose is to enable better medicines by providing sustainable pharmaceutical materials through innovative and customized solutions. Our product range consists of Quaternary ammonium compounds (Quats), Recombinant Insulin, Customized Purification Resins, and Specialty Enzymes.
Contact
For further information about the position please contact Senior Manager Jan Karkov Carstensen on mobile number +45 31 99 59 11.
Deadline
21 May 2023
Applications will be evaluated continuously, and candidates may be called for an interview before the deadline, so please apply as soon as you can. You do not need to attach a cover letter to your application, but please include a few lines about your motivation in your resume or CV. Additionally, please avoid the use of photos in your CV. This provides a better and more fair 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.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Køge.
Jobbet er oprettet på vores service den 9.2.2023, 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.
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