- Microsoft
- Noord-Holland
- 3 dagen geleden
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...medical care leave, gender identity or expression, genetic information, immigration status, marital status, medical condition, national origin, physical or mental disability, political affiliation, pr...
- Johnson & Johnson
- Gelderland
- 3 dagen geleden
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...other local requirements together with other department. Maintain the validation master plan (VMP) and procedures, and ensure alignment with the company's quality management system. Establishing metri...
- Microsoft
- Noord-Holland
- 3 dagen geleden
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...medical care leave, gender identity or expression, genetic information, immigration status, marital status, medical condition, national origin, physical or mental disability, political affiliation, pr...
- Universiteit Utrecht
- Utrecht
- 1 week geleden
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...other scientists, including colleagues from other departments. You will apply for external funds, supervise PhD candidates and postdocs, and organise relevant scientific meetings at national or intern...
...medical device. While working in an open culture, we strive for excellence in all domains. We believe in taking courage and like to challenge each other. We learn and teach, regardless of age, nationa...
...medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected charac...
- Philips
- Noord-Brabant
- 1 week geleden
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...Medical device Quality and Regulatory domain. You are responsible for Successful completion of Quality and Compliance Program across Image Guided Therapy Cluster with focus on Standardization, and Con...
...other COE stakeholders. Ensure the Total Rewards function continuously evolves its offerings to meet the changing needs of a high-growth, science-driven organization. Executive Compensation & Governan...
- Thermo Fisher Scientific
- Nederland
- 1 week geleden
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...medical affairs, health economics and outcome scientists to ensure high-quality and compliant deliverables in a timely manner that support real word evidence generation and regulatory submissions. Key...
- Johnson & Johnson Innovative Medicine
- Zuid-Holland
- 1 week geleden
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...other functions and teams in Therapeutic Areas, Global Development, Regulatory Affairs, Data Sciences, Clinical Data Standards and others as needed. External: Interact and collaborate with vendors. Ac...
...Medical Monitor , you will play a key role in ensuring the safety and well-being of clinical study participants and upholding the integrity of the studies. You will provide medical oversight, manage s...
- AbbVie
- Overijssel
- 1 week geleden
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...medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and servi...
- Philips
- Noord-Brabant
- 1 week geleden
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...Medical Devices Industry or equivalent. Extensive knowledge on (non-)Medical Device development standards (e.g. ISO13485) and regulations (e.g. 21CFR820, EU MDR) and FDA 510K Extensive experience with...
- Amaris Consulting
- Noord-Brabant
- 3 dagen geleden
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...other people related to your future role. We will talk in depth about you, your experience, and skills, but also about the position and what will be expected of you. Of course, you will also get to kn...
- Danone
- Zuid-Holland
- 3 dagen geleden
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...Medical Devices (NMD) team through various HR projects and HR cycle (for example Talent Review process), data analysis with our HR dashboard, and much more. Your Main Responsibilities Include Provide ...