Regulatory Affairs Specialist
Haifa, Israel
Job Description
- Novocure has ongoing or completed clinical trials and is further expanding its efforts into several other solid tumor indications - non-small cell lung cancer, pancreatic cancer, and other types of solid cancers.
The Regulatory Affairs Specialist will be part of the Global Regulatory Affairs team and will be responsible for supporting the team in the preparation of documentation for regulatory submissions required to market new or modified medical devices. This full-time position reports to the Director, Regulatory Affairs, and is placed in our Haifa office, Israel..
Support in the preparation and management of documentation for global regulatory submissions in a timely manner.
- Support in the preparation of responses to regulatory queries from global regulatory authorities.
- Organization and maintenance of records and correspondence with all parties involved in the regulatory document control center.
- Maintain processes and monitor practices to ensure regulatory compliance.
- Research regulatory issues and provide guidance and advice to colleagues.
- Assist in the research and dissemination of global regulatory intelligence topics.
- Liaise with cross functional teams such as engineering, QA, supply chain, pre-clinical and clinical development on projects
QUALIFICATIONS/KNOWLEDGE:
- Qualifications:
- MSc degree in life sciences
- Knowledge:
- 5+ years of experience in regulatory affairs and/or QA within the Medical device/ pharmaceutical industry.
- Knowledge of international regulations for the EU, US, Japan, China and others
- Knowledge of the ISO 13485
- Experience in writing procedures and regulatory documents
- Fluent in English, both written and spoken, and other European languages is an advantage
- Ability to work consistently and effectively as part of a team
- Attention to detail
- Ability to work under pressure to meet aggressive deadlines
- Critical thinking, reasoning, and problem-solving capability
- Excellent Office software proficiency
OTHER:
- Excellent organizational and time management skills
- Highly motivated and quality oriented
- Excellent communication skills
Apply
Career Focus: Regulatory, Admin, Regulatory/Compliance
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