Gewährung von Lizenzen

BRINE SA has been placing top specialists at well-known customers for over 30 years. In doing so, we focus on performance, competence, experience and partnerships

Job Purpose/ Role:

• Execute manufacturing activities in the area of Drug Product according to cGMP guidelines, ensuring batch execution, evaluating test results
• resolving issues, troubleshoot manufacturing equipment and make recommendations for resolution
• Provide front line technical and procedural support, working with the manufacturing team
• Securing each batch is manufactured safely, on time, in compliance with the batch instructions and quality requirements
• Responsible to establish timely and with high quality the required production documentation (preparation, execution and review of batch records) or other relevant GMP documents for the assigned production area
• Support process related investigations and assists in decision making on production issues
• Support process changes and CAPAs related to processes within required timelines Perform training activities of relevant areas as operator and supports others and new joiners
• Operating, setting up and cleaning production equipment and premises for the production of liquid and freeze-dried drug forms (e.g. compounding, parts washing, autoclaving, filter integrity testing, visual inspection)

Du solltest haben:

• 2-4 years of experience GMP environment on the shopfloor (preferably in sterile manufacturing of Drug Product)
• Familiarity with GMP requirements, quality procedures and SOP execution
• Strong team orientation
• Good communication skills and interaction with a variety of interfaces within the organization
• Structured, focused and well-organized working attitude
• High motivation and dynamic drive
• IT knowledge and knowledge in SAP and MES is a benefit
• Prepared to work flexible working hours
• Fluent in either English or German (preferably both)

You’ll receive further information at an interview

Fluent English (oral and written) and/ or German