Description
A Global Biotechnology organisation, based in Denmark, is currently looking to add to their internal process Engineering team, during a period of increased project activity.The role:
• To act as responsible engineer on behalf of the site group and interface with external engineering consultancies/commissioning providers.
• Review and preapproval of commissioning/validation protocols and the support in execution of commissioning/validation.
• Conducting trouble shooting, walk downs and P&IDs.
• Conducting the review of associated engineering documentation.
Requirements:
• Previous experience working, within a highly regulated Biotech/Biopharma organisation.
• Experience in supporting standard commissioning activities for a GMP facility or project.
• Understanding of basic principles in validation and an appreciation of cGMP standards.
• Willingness and ability to perform hands on trouble shooting of equipment and processes.
• Previous experience of working within a multi-disciplined project matrix.
• An understanding of Automation systems/Delta-V DCS would be beneficial.