CIP/SIP Validation Specialist/Engineer - Aptio Group Denmark Aps

CIP/SIP Specialist or Engineer with an interest in pharma
We are looking for you, who has years of experience and knowledge working with CIP/SIP within the pharma industry, can manage and coordinate engineering activities and have the ability to ensure overall coordination of CIP/SIP processes. The project is based in the Greater Copenhagen area.

Main Responsibilities:

• Management and coordination of engineering activities regarding CIP (Cleaning In Place) and SIP (Sterilisazation In Place) with external partners and internal stakeholdes.
• Review CIP/SIP design
• Work with CIP/SIP strategy
• Review of user requirements regarding CIP/SIP
• Coordinate with external partnes and internal stakeholders to ensure overall coordination of the CIP/SIP design

Requirements:

• Minimum 5 years related experience cleaning & sterilisation from either validation or engineering in pharmaceuticals
• Knowledge of and experience with CIP & SIP validation and design within the pharma industry
• Engineering Degree (Mechanical or Chemical) or equivalent technical training and experience

Are you curious to know more about the position, do not hesitate to contact us

All applications must be submitted in English and are treated confidential.

Submit your CV and resume in the below form