Vacature Quality Control Working Foreman
Applikon Biotechnology B.V., a part of Getinge since 2020, is a Dutch high-tech company and a world leader in the development and supply of advanced bioreactor systems from the laboratory to the pilot and production scales. Our mission is to offer reliable solutions that make it possible to save lives. We support the pharmaceutical industry (vaccines, regenerative drugs, antibodies, body tissues, biopharmaceutics and biosimilars) as well as industrial microbiology (enzymes, food & beverage, nutraceuticals, biofuels, biochemicals, and bioplastics) in their upstream processes. Our main office is located in Delft (Netherlands) with subsidiaries in the USA and UK. We have more than 180 employees working worldwide on product development, production, quality control, marketing & sales, and after-sales support - all of which contributes to improvements in Life Science. That is our passion!
The QC Department is looking for a:
Quality Control Working Foreman (IC-AC)
As the working foreman (IC-AC) you will lead (organize, motivate, check, stimulate and plan) the employees performing the Entrance Inspection (IC) and the Final Inspection of Standard (non-stainless steel) systems (Check out). You will directly supervise the activities of the employees and help establish the work/production times. You will manage, manufacture and maintain the available tools and KMB resources. You will advise on the use of the correct KMB resources for inspection plans and you will supervise the ESD safety provisions. During control, you will perform representative samples. You will also make the inspection files available to executives and, where necessary, provide instruction. An important task is that you will ensure the correct application of standards, regulations and procedures.
You will carry out inspections and acceptance tests based on the project planning. You will check the delivered products in accordance with the requested specification on the order form, drawing, bill of materials or other enclosed instruction. You will check for completeness of the configuration, manuals and checklists in the assembly file, or the written report on problems, deviations and findings. You will review and release inspection protocols (IV, OV, FAT and SAT) and manuals for standard systems and simple projects. You will ensure that quality deviations are fed back to the QC Manager in a timely manner.
You will check the functionality of the tested equipment, and whether it is complete before shipment.
This also includes taking care of purchase by the customer (possibly with assistance from the Product Management, Project Management and/or Process Engineering departments). You will be responsible for the registration of the activities in the ERP system.
You have experience in performing and managing QC activities. In addition, you will acquire excellent knowledge of the product range and measurement setups. You have adequate materials knowledge and knowledge of validation documentation and you have or will acquire knowledge of the functioning of bioreactor systems and peripheral equipment. You work accurately and independently and you have good communication and didactic skills. In addition, you have good computer system skills, allowing you to work easily in a digital environment.
Knowledge, skills and experience
- You have completed education at the Dutch MBO WTB/E level, or laboratory training.
- You have adequate written and spoken command of the English language.
- You are familiar with cG(A)MP and you have good knowledge of ESD safe working, measurement and control technology, and SCADA systems.
- You can work well in a digital environment and quickly learn to use new software applications.
- You are in possession of a Dutch B driving license.
If you are interested in working in a dynamic organization with short communication lines and an informal culture, and where innovation and professionalism are of paramount importance, then please send your application.
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