Senior Automation & IT Compliance Consultant
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Virum
Working in pharmaceutical and biotech production environments that become increasingly digitalized requires a lot of knowledge of software validation and verification as well as experience in keeping and preserving the validated state of computerized equipment. At NNE we build new GMP facilities, we upgrade, or revamp existing facilities and we work with design, implementation and validation of Automation, IT, MES and Laboratory systems. Compliance consultancy is a core ingredient in all our solutions. We are currently looking for a new senior Automation and IT compliance consultant to strengthen our team in this area.
Primary Duties and Responsibilities: You will work independently or as part of a team to help our customers with for example:
• Quality planning
• Requirement specifications
• Quality Risk Management
• IT risk assessments
• Test and verification
• IT compliance assessments
• General IT Compliance consulting
Required Qualifications: You have a relevant academic background (Bachelor or Master degree). You have worked in the area of quality management of computerized systems in a pharmaceutical or biotech environment. You 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 5-10 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 3079 0509.
Deadline of application is 3/1/2020
Primary Duties and Responsibilities: You will work independently or as part of a team to help our customers with for example:
• Quality planning
• Requirement specifications
• Quality Risk Management
• IT risk assessments
• Test and verification
• IT compliance assessments
• General IT Compliance consulting
Required Qualifications: You have a relevant academic background (Bachelor or Master degree). You have worked in the area of quality management of computerized systems in a pharmaceutical or biotech environment. You 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 5-10 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 3079 0509.
Deadline of application is 3/1/2020
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Virum.
Jobbet er oprettet på vores service den 4.2.2020, 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
- Virum
- Søndag den 01. marts 2020
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