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Transfer Production Coordinator
Liege, Belgium
As a leading innovator of women’s health, we at Hologic are empowering people to live healthier lives everywhere, every day.
Our manufacturing and operations teams sit at the core of what we do as a business, combining production, supply chain and operations. From improving quality, reducing costs, speeding throughput our manufacturing and operations teams enable us to meet and exceed our customer expectations, driving us to be the best.
As our Transfer Production Coordinator, you will ensure that any development in R&D can be produced by the manufacturing team, following ISO standards. Your experience ensuring the validation and improvement of production, processes and instruments will help you to excel.
WHAT TO EXPECT
Assist in the development of new products or a new process, ensuring the technical improvement of products currently on the market and existing production processes.
Writing, adapting and implementing procedures, work instructions and forms for Production Department.
Inventory of raw materials needed for production (BOMs and raw material doc tracker).
Protocols and reports linked to the product transfer between R&D and Production Departments (Process Transfer Review, Protocol and Report).
Hold responsibility for the Device Master Record.
Assist in training the production team on the output of the transfer documentation.
Reviewing and approving R&D documentation for product development.
Reviewing and approving product, process and instrument validation documentation.
Reviewing and approving global project documentation.
Assisting the validation team in the implementation of the protocols related to the validation of the products, processes and equipment.
Manufacturing and release of product development lots.
Assisting production team for manufacturing validation lots.
Training and assisting QC department in the testing and release during new product development.
Technical improvement of products currently on the market, and existing production processes.
Creation and follow up of project timeline with core team members.
WHAT WE EXPECT
1 – 5 years’ experience working to ISO 13485 quality standard and regulations
Degree in biology, molecular biology, biochemistry or equivalent
Proficiency in molecular biology techniques (PCR)
Knowledge of product validation and transfer principles
1-5 years of experience in a similar field and work experience in ISO 13485 environment
Languages: French and English
Organized, autonomous, good planner, able to handle multiple tasks in parallel
So, why join Hologic?
A chance to be part of a globally recognized leader in healthcare.
A stimulating work environment that encourages innovation and personal growth.
Competitive salary and comprehensive benefits package.
Join us today and be a part of shaping the future of global healthcare. Your expertise is invaluable, and together, we can make a difference!
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