Automation & IT Compliance Consultant
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Kalundborg
When we go to work, we empower our customers to make life safer and healthier for millions of people who depend upon their medicine. As one of the world’s leading engineering and consulting companies within life sciences, NNE doesn’t have any manufacturing lines or facilities ourselves. But we take pride in ensuring that companies like Novo Nordisk, LeoPharma, AJ vaccines and many others can bring vital treatments to patients. NNE’s Automation area is looking for an Automation & IT Compliance Consultant. Our department is engaged in automation solutions for pharma production for the pharmaceutical and biotechnological industry, with focus on production control and computer solutions for the processes. We work with design, implementation and verification/validation of Automation, IT, MES and Laboratory systems. GMP compliance consultancy is a core ingredient in all our solutions. </font
Primary Duties and Responsibilities: As a member of the leading automation supplier within Pharma, you will be an active part of our project teams, where we focus on personal development and knowledge sharing. You will be part of a small cross-functional consulting team with more than 250 years of total experience in the pharmaceutical manufacturing domain. Each of our specialists holds industry leading know-how within key concepts or technologies.
Your role as compliance consultant will be to strengthen our team in Virum and Kalundborg within:
Required Qualifications: You have a relevant academic background (Bachelor or Master degree). You are passionate about working in the area of quality management of computerized systems in a pharmaceutical or biotech environment. You might have experience with Automation & IT technologies like PLC, SCADA, DCS or MES systems. You are familiar with the US and European GMP rules, the GAMP guide, the ASTM-2500 and the ICH guides.
We expect our new colleague to have at least 3-5 years of relevant job experience. It is essential for the position that you are open-minded and not afraid to take up different kinds of assignments.
As a person, you are proactive and passionate about your job. You are result-oriented and have a well-structured approach to your work. You have excellent customer understanding – and the ability to inspire and demonstrate leadership in customer relations.
Finally, you speak and write English and Danish fluently.
If you have any questions about the job, please contact Director Henrik Pedersen, +45 30790509.
Deadline of application is 15 December 2020.
We will invite to interviews on a running basis.
Primary Duties and Responsibilities: As a member of the leading automation supplier within Pharma, you will be an active part of our project teams, where we focus on personal development and knowledge sharing. You will be part of a small cross-functional consulting team with more than 250 years of total experience in the pharmaceutical manufacturing domain. Each of our specialists holds industry leading know-how within key concepts or technologies.
Your role as compliance consultant will be to strengthen our team in Virum and Kalundborg within:
- Participate in / drive quality plannings
- Give input to requirement specifications
- Participate in Quality Risk activities
- Contribute to IT risk assessments
- Contribute and supervise test and verification
- Conduct IT compliance assessments
- Provide general IT Compliance consulting to customers
Required Qualifications: You have a relevant academic background (Bachelor or Master degree). You are passionate about working in the area of quality management of computerized systems in a pharmaceutical or biotech environment. You might have experience with Automation & IT technologies like PLC, SCADA, DCS or MES systems. You are familiar with the US and European GMP rules, the GAMP guide, the ASTM-2500 and the ICH guides.
We expect our new colleague to have at least 3-5 years of relevant job experience. It is essential for the position that you are open-minded and not afraid to take up different kinds of assignments.
As a person, you are proactive and passionate about your job. You are result-oriented and have a well-structured approach to your work. You have excellent customer understanding – and the ability to inspire and demonstrate leadership in customer relations.
Finally, you speak and write English and Danish fluently.
If you have any questions about the job, please contact Director Henrik Pedersen, +45 30790509.
Deadline of application is 15 December 2020.
We will invite to interviews on a running basis.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Kalundborg.
Jobbet er oprettet på vores service den 27.10.2020, 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
- Kalundborg
- Tirsdag den 15. december 2020
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