Process Validation Engineer
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Do you have experience with the implementation of processes within GMP? And would you like to join an exciting growth journey in a supportive environment, where we help each other succeed? Then you might be one of our new Process Validation Engineers at Novo Nordisk Pharmatech in Køge. Apply today and join us for a life-changing career! The Position You will join a newly established team where you will support our project department and upcoming production facility with effective, reliable and stable high-quality solutions. More specifically, you will contribute with:
You will work closely together with our Process Validation Scientists, Equipment Validation Engineers and Scientists, Quality Assurance and many other highly engaged colleagues. We are very proud of our supportive culture, where we take pride in learning from our mistakes and empowering each other to succeed. We are looking for several new colleagues so please do not hesitate to apply if this job sparks your motivation. Qualifications To qualify for the position, we imagine that you have a technical background in dairy, laboratory work, as a process operator or similar. Most importantly, you have experience with chemical processes from a regulated manufacturing environment. Moreover, you have all or most of the following qualifications:
It is an advantage if you are also experienced in IT and have an interest in Programming. Maybe you have knowledge of production IT systems as SAP and SCADA. As a person, you are a dedicated team player, who is energized by watching your team succeed and knowing you had a part in it. You are strong-willed when it comes to finding a solution to a problem and have a positive and constructive mindset in the face of adversity. About the team Project Support is a newly established team who is working closely together with our project department. The team consist of 10-12 skilled academics and technicians who support our projects with the process- and equipment knowledge. 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 our Project Support at the site Køge, 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 Manager for Project Support Dorthe Christensen on mobile number +45 31 97 00 32 Deadline 19 March 2023. We will process applications as we receive them, so please do not hesitate to apply as soon as you can. 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. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. 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.
- Participate in end-to-end processes (determine business needs, create user requirements specifications, design solutions and write documentation such as procedures and change requests)
- Validate the process and ensure a high level of quality
- Implement operational standards and ensure that all quality- and safety input are adjusted and implemented
- Evaluate if the system is qualified and fit for the intended use, based on design and verification activities
- Experience working on projects with design, implementation and validation of processes
- Ability to make concrete requirements to production equipment
- Knowledge within automation, regulation and measurement techniques
- Experience writing documentation and ensuring compliance
- Professional proficiency in both Danish and English, verbal and written
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 28.2.2023, 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.
- Øvrige
- Køge
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