Document Management Lead
17 godzin temu
- Lead the preparation and submission of regulatory documents for product registration and compliance;
- Coordinate the work of a team to ensure timely and accurate delivery of documents;
- Develop and implement plans for document management and regulatory compliance;
- Collaborate with internal stakeholders to ensure effective communication and coordination;
- Bachelor's degree in a relevant field (e.g., life sciences, law, or business);
- Minimum 5 years of experience in regulatory affairs, preferably in the pharmaceutical industry;
- Proven track record of managing teams and coordinating complex projects;
- Strong knowledge of regulatory requirements and guidelines;
- Excellent communication and interpersonal skills;
- Ability to work in a fast-paced environment and prioritize multiple tasks effectively.
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Warszawa, Mazovia, Polska Randstad Polska Sp. z o.o. Pełny etatJob DescriptionRandstad Polska Sp. z o.o. is seeking a highly skilled Regulatory Affairs Specialist in Electronic Document Management to join our team. As a key member of our team, you will be responsible for maintaining regulatory information in a secure environment to enable access, retrieval, and integrity.Key Responsibilities:- Archives electronic...
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Document Coordinator
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