Regulatory Affairs Vacatures in Zuid-Holland
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Zoekresultaten - Regulatory Affairs Vacatures in Zuid-Holland
Avery Dennison-Oegstgeest
Avery Dennison in the Netherlands seeks an EMENA Regulatory Affairs Manager to lead EU regulatory strategy, ensure product compliance across Europe, and support market access for growth.
You will manage submissions and certifications, coordinate...
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Avery Dennison-Oegstgeest
Compensation: EUR 77700 - EUR 124320 - yearly
Job Description Role Overview
The EMENA Regulatory Affairs Manager oversees regulatory compliance and affairs for the business group across Europe, the Middle East, and North Africa. This position acts...
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ONYX Power-Rotterdam
ONYX Power is op zoek naar een Country Lead Public & Regulatory Affairs in Nederland, gevestigd in Rotterdam. Je bent verantwoordelijk voor publieke en regelgevende aangelegenheden en stakeholdermanagement met overheid, regulators en de Port...
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Qabird-Leiden
and deviations, and maintain GMP documentation while collaborating with Manufacturing, QA, Regulatory Affairs, and external partners. English fluency and travel are required.
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SIRE LIFE SCIENCES-Rijswijk (Z-H)
SIRE LIFE SCIENCES is seeking an experienced Regulatory Affairs Specialist for a temporary maternity-cover assignment based in Rijswijk, NL. You will support the Benelux regulatory framework, collaborating with Brussels colleagues to ensure product...
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Pharming Group-Leiden
Control, Regulatory Affairs, Supply Chain and external partners to support reliable product release and overall quality oversight. You will review release documentation, manage deviations and CAPAs, author GMP documents, and act as the primary QA contact...
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SIRE Group-Rijswijk (Z-H)
SIRE Group seeks an experienced Regulatory Affairs Specialist for a maternity cover in the Benelux region, based in Rijswijk. The role focuses on ensuring product compliance, enabling innovation, and acting as a regulatory partner to support...
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Pharming Group-Leiden
colleagues in Manufacturing, Quality Control, Regulatory Affairs, Supply Chain, and external partners such as contract manufacturers, laboratories, and suppliers.
What will you do?
Review, assess and prepare QA release packages for clinical and commercial...
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Johnson & Johnson Innovative Medicine-Leiden
single submission.
We are searching for the best talent for Principal Scientist (Manager), Global Regulatory Affairs, CMC. This is an onsite/hybrid role.
Purpose The Principal Scientist of Global Regulatory Affairs CMC is responsible for developing...
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Unitron-Leiden
Regulatory Affairs Project Manager
Medical Devices
Jij brengt duidelijkheid in een wereld vol regels
Regulatory Affairs Project manager
Jij brengt duidelijkheid in een wereld vol regels
Regulatory Affairs Project Manager
Medical devices
Jij...
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werkenbijunitron.nl -
Pharming Group-Leiden
and guidelines (e.g. FDA, EU, ICH and national).
The Senior Manager CQA leads and develops the CQA team and partners with Clinical Development, Medical Affairs, Pharmacovigilance, Regulatory Affairs and external service providers to safeguard participant safety...
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workinthehague.nl -
ProQR-Leiden
guidance and scientific advances in toxicology and RNA therapeutics, translating new insights into development strategies.
• Build strong collaborations across Research, Translational Development, Clinical Development, Regulatory Affairs, CMC, and external...
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proqr.com -
Stichting PUM senior experts-Den Haag
Chemical - Pharma (EU certification pharma products, chemical distillation, pharmaceutical regulatory affairs, cosmetics). - Metal (surface treatments, adhesion technology, technological process improvement).
• You are an authentic, resilient, humble...
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pum.nl -
Eneco-Rotterdam
voor
• Proactieve bijdrage aan het verhogen van de performance van District Heating door het sturen op waardecreatie;
• Richting geven, adviseren en coachen van de stakeholders op het gebied van nieuwe regelgeving WcW in samenwerking met Regulatory Affairs...
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werkenbijeneco.nl -
Qabird-Leiden
colleagues in Manufacturing, Quality Control, Regulatory Affairs, Supply Chain, and external partners such as contract manufacturers, laboratories, and suppliers.
What will you do?
Review, assess and prepare QA release packages for clinical and commercial...
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