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Our client is a global biopharmaceutical company focusing on creating value for people living with neurology and immunology.
You have at least 5 years experience in a pharmaceutical/chemical industry in a laboratory or manufacturing environment? You have experience in equipment implementation?
Don't hesitate to contact me : email@example.com
Coordinates, plans, tracks and monitors all pilot plant activities especially regarding equipment implementation in alignment with the Pilot Plant Management
Ensures good collaboration with all customers and stakeholders of the pilot plant and warehouse and provides active scientific and technical guidance/support to them
Develops and maintains fit-for-purpose equipment that are compliant with all relevant regulatory guidelines and SOPs
Provides and defines efficient workflows and business processes especially regarding equipment in alignment with Pilot Plant Management
To lead the benchmarking, purchasing and qualification/validation activities for new equipment for the pilot plant
To communicate the planning, activities, due-dates, attention points to all stakeholders of a project
To support all co-workers and stakeholders (QA, metrology, qualification, maintenance and site facilities) of the Prod Dev Pilot plant and warehouse area with technical assistance and coordination of technical activities
To provide appropriate documentation for all quality related activities
To support the development and maintenance of an overall process to ensure that all equipment are in an appropriate condition ready for pharmaceutical use
To train co-workers in the field of quality/safety related technical operations
To ensure cGMP compliance of premises, equipment and procedures within the pilot plant and warehouse area as determines by the manager
To ensure quality assurance activities are carried out in time
To apply all relevant regulations, guidelines and operating procedures (regulatory, quality and safety)
Min 5-7 years’ experience in a laboratory or manufacturing environment, preferably in pharmaceutical or chemical industry
Experience in a GMP regulated environment
Experience in both R&D and commercial manufacturing of the pharmaceutical industry is an asset
Very good administrative, organizational and documentation skills are mandatory
Good knowledge in English is mandatory
Ability to communicate and collaborate within the team, Product Development department
To be observant, identify or prevent from problems or issues and to raise them with supervisor when necessary
Consistently will to improve processes: SOP, business processes ...
Ability to prioritize activities in alignment with supervisor
Ability to delivery in a changing development environment
Working with Trackwise, Source, SAP is a huge asset
wat bieden wij?
We offer an attractive salary with extra-legal advantages :