Quality Control, GMPs, bioanalytical method validation.• Strong knowledge of GMP, SOPs and quality control processes.• Identifying, writing evaluating and closing OOS’s and investigations.• Experience with MS office• English needs to be fluent(Strong written and verbal communication skills)• Minimal PhD
GRAs, Audits, Teva Global Standard implementation to ensure sustainable compliance. o Write study protocol and report as part of failure investigations. o Actively participate in advanced problem solving, root cause analysis, troubleshooting, interpretation/consultation, verification of quality and test
commitment, GRAs, Audits, Global Standard implementation to ensure sustainable compliance. o Write study protocol and report as part of failure investigations. o Actively participate in advanced problem solving, root cause analysis, troubleshooting, interpretation/consultation, verification of quality and
waar eerlijkheid, transparantie en kwaliteit tot de kernwaarden behoren? Solliciteer dan snel en kom op gesprek!Role DescriptionAls Quality Control Officer werk je in een snel groeiende afdeling waar de kwaliteit van alle producten gewaarborgd wordt. Jij ondersteunt de analisten bij het uitvoeren van
a professional organisation, based in Utrecht Netherlands.The CompanyThis company started as a family owned business and is continuing to further professionalize their organisation to keep up with their ever growing client base.Role DescriptionAs QC-specialist you'll be supporting the Quality department in
a professional organisation, based in Gelderland Netherlands.The CompanyThis company started as a family owned business and is continuing to further professionalize their organisation to keep up with their ever growing client base.Role DescriptionAs QC-specialist you'll be supporting the Quality department in
SIRE Life Sciences® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced ...
they are looking for a new QA specialist specifically experience with FDA and Design control.Role DescriptionYou will work in an international team within the company that focusses on document control aspect of FDA. You will guide the project team through the Quality requirements of designing a variety
Responsibilities: Achieve the results proposed by the organization through monitoring and achievement of pre-established metrics, coordinating the team of quality through meetings, trainings and issue tracking solutions. Ensure that current products and new products meet the quality requirements defined by our
DirectorRequirements- Agricultural Engineer or similar, with Dairy Technology background - Quality competences : HACCP, ISO, IFS, BRC, hygiene , analysis and statistic tools - Experience of minimum 7 years in Quality within Food Industry, preferable Dairy - conviction, persuasive, empowering - be able to cope
onderhouden en verbeteren van het kwaliteitssysteem, volgens de ISO-13485 norm.Responsibilities- Het organiseren en geven van trainingen- QA reviews voor batch release- Document control, Change control- Deviaties en non-conformances- Assisteren in kwaliteitsplanning, meetings van management reviews
a professional organisation, based in Anvers Belgium.The Companyour client is a professional organization of fruit in the food industry. based in Antwerp.Role Description- As a Quality Director you will be responsible for the quality policy in production sites : belgium and 3 other countries. You will also be
management tools: FMEA, PPAP, 8D, Control Plan, 5 WHY, QRQC, Ishikawa, Knowledge of statistical methods (SPC), Ability to use the quality techniques and tools in practice, Ability to use the technical documentation (drawings, standards), VDA 6.3 or QSB audit experience. We offer ...
Director and QP.Responsibilities- Review and approve Batch records - Provide support to Qualified Person- Coordinate and follow up on quality incidents, deviations and customer complaints.- Define and follow up on corrective actions and preventive actions (CAPA).- Coordinate and follow up on any relevant
support the quality coordinators with their quality related projects.- Set-up and monitoring the control limits for main process and quality characteristics.Requirements- BSc (preferable in the direction of Food technology of Engineering) - Affinity with Engineering - Knowledge of ISO 9001:2015, HACCP
zijn zij zeer innoverend, pro-actief nieuwe oplossingen aan het bedenken en groeien ze jaarlijks nog zo een 20%! Ongeveer 500 miljoen omzet.Role DescriptionOp zoek voor locatie omgeving Tilburg. Als Quality Engineer ben je samen met je Quality engineer collega's verantwoordelijk voor het ontwikkelen ...
eindproducten: Controle van aangeleverde bewaarmonsters; Toezicht houden op het opslaan van bewaarmonster onder juiste omstandigheden (temperatuur, luchtvochtigheid en licht); In en uitboeken van monsters middels een archiveringsdatabase; Toezien op correcte vernietiging van
system. Further responsibilities are: • You will be on track with the latest developments and changes of QA within the Medical Devices sector• Development of strategic plans and implementation tools for the improvement of the Quality Management System• Overview and collect required documentation and