Process Validation Scientist
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Køge
Would you like to work with the implementation of processes within GMP (Good Manufacturing Practice)? 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 Scientists 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 can look forward to:
You will work closely together with our Process Validation Engineers, Equipment Validation Engineers and Scientist, 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 empower 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: Academic education within Engineering, Life Sciences or similar Strong competences within process validation and operational process. Some years of experience working on projects, including the design and validation of process. Ability to make concrete requirements to production equipment and knowledge within automation, regulation and measurement techniques. Very good communication skills in English and Danish. 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 enjoy finding a solution to a problem and have a positive and constructive mindset in the face of adversity. About the department Project Support is a newly established team who is working close together with our project department. The team consist of 10-12 skilled academics and technicians who support our projects with 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 has 300+ employees and is 100% owned by Novo Nordisk A/S. The ability of Novo Nordisk Pharmatech A/S to produce and deliver quality products to the pharmaceutical industry, combined with our complete range of services within regulatory requirements, makes us a preferred supplier to many global pharmaceutical companies. Novo Nordisk Pharmatech A/S is a fast-growing company generating many exciting projects and offering excellent development opportunities. 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.
- Participating in end-to-end processes (determining business needs, creating user requirements specifications, designing solutions and writing documentation such as procedures and change requests)
- Validating the process and ensuring a high level of quality, giving inputs to design and approving Design Qualification
- Implementing operational standards and ensuring that all quality- and safety input are adjusted and implemented
- Evaluating if the system is qualified and fit for the intended use, based on design and verification activities
- Approving Acceptance Criteria for URS requirements - Acceptance Criteria for PQ, PV, System Acceptance and Release (SAR) and Decommissioning Plan and report
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 27.2.2023, 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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