Job Description
During the project phase:
• supporting commissioning and validation activities of the site with a strong focus on our Downstream equipment including Column Packing and BDS Dispensing, working in close collaboration with the Engineering teams.
Once the site will be operational, your role will include (but will not be limited to):
• Preparation and assembly of production equipment
• Assembly and testing filtration systems
• Pilot and Execute related purification operations and/or manufacturing support activities using Delta V and electronic batch records for the in accordance to GMP regulations
• Revise Electronic Documentation as instructed: Key documentation includes eBR’s (electronic Batch Records) and electronic logbooks
• Report and assist on production deviations
• Participate in the training and onboarding of your new colleagues
• Be proactive in Continuous Improvement for your working station
4 Shift work will be required as of 2019
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Qualifications
• A first solid experience in Purification Production within Biotechnology or Pharmaceuticals
• Excellent practical knowledge and application of cGMP compliance and other related regulations
• A Good level of English is mandatory: our work instructions (SOPs) are in English
• You are technically sound and possess a strong understanding of automated systems and process controls
• Ability to work in a dynamic environment with frequent interruptions, changing priorities and deadlines
• You are a good team player and bringing a positive and constructive attitude
Education
Apprenticeship or technical degree in chemical, Pharma or Biotech production or equivalence