-As Production Process Engineer you will be responsible for “how the line is operated” and production issues related to this (CR’s, NC’s). In addition to this, your responsibilities would include:
-SOP writing (own A1-A10, PM schedules including WO)
-Change control of above SOPs
-Inspections and audits (audit preparation including those leading to PQ and submission to authorities
-Support/Maintain Operational Training (Competence Matrix, KPI’s)
-Review log books
-EHS (ensure EHS compliance)
-Ensure Compliance to NN Validation Strategy, SOP’s and principles
-CR handing as CR owner, affected party, action owner
*Look forward to a job in an international organization that has great ambitions, challenging tasks, diversity throughout and plenty of opportunities for you to realize your full potential and professional ambitions.
-Engineering degree within Mechanical, Electrical, or similar field
-Over 3 years of industrial experience in maintaining production equipment in a compliant state with respect to authority requirements in GMP environment (pharma, food or cosmetics)
-Need an open mindset who can work independently and as a team player with a strong focus on results
-Further to this, you should have good communication skills with the ability to establish good relationship with local and global team
-Be fluent in English, both written and oral
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Novo Nordisk Pars
Novo Nordisk is a world leader healthcare company in diabetes care, having the broadest diabetes product portfolio in the industry, including the most advanced products within the area of insulin delivery systems. In addition, Novo Nordisk has a leading position within areas such as haemostasis management, growth hormone therapy and hormone replacement therapy. Novo Nordisk manufactures and markets pharmaceutical products and services that make a significant difference to patients, the medical profession and society.
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