Regulatory Scientist supporting product compliance, scientific documentation, and regulatory submissions in hybrid environment. Join the Regulatory Affairs team in Stockholm for product safety and compliance.
Responsibilities
Ensure compliance with international and national laws, including REACH, CLP and EU TPD by participating in product development and innovation project meetings and providing relevant regulatory framework.
Prepare, review, and submit regulatory documentation in accordance with applicable standards and internal procedures.
Conduct scientific assessments and data evaluations to ensure product compliance.
Support internal teams in regulatory and technical matters related to product portfolios.
Collaborate with R&D, Quality, and Product functions to ensure timely and accurate submissions.
Participate in continuous improvement of regulatory processes and documentation practices.
Requirements
Bachelor’s or Master’s degree in Chemistry, Chemical Engineering, or a related scientific discipline.
Minimum of 3 years of experience in regulatory, scientific, or compliance-related work.
Proven experience performing similar tasks within life science, chemical, or consumer product industries.
Fluent in both Swedish and English, spoken and written.
Excellent interpersonal and communication skills, with the ability to effectively engage with internal stakeholders.
Strong analytical and problem-solving abilities, with attention to detail.
Compliance Assistant managing sales data delivery to contracted vendors. Conducting data quality checks and maintaining vendor relationships at Hudson.
Ethics & Compliance Manager leading compliance activities and protecting KONE’s reputation. Driving implementation of ethical programs across KONE India with focus on integrity and compliance.
Manager/Director, Technical Regulatory managing regulatory submissions for pharmaceutical products. Ensuring compliance with local and global standards in order to support timely approvals.
Corporate Compliance Clerk supporting Business Law team in London, Ontario, maintaining minute books and preparing corporate documentation. Requires 3+ years' experience and offers a hybrid work arrangement.
Senior Regulatory Specialist managing regulatory activities for pharmaceutical CMC projects. Collaborating with diverse teams and ensuring timely delivery of regulatory documentation and compliance.
Director of Regulatory Affairs leading drug product regulatory strategy and team management. Ensuring compliance and managing communication with FDA and regulatory bodies in a pharma environment.
Senior Consultant managing Compliance projects in the medical devices sector with a focus on Quality & Regulatory. Collaborating with a dynamic team in a leading GMP - expert company.
Senior Project Engineer focusing on GMP Compliance in the Life Sciences sector. Responsible for project planning, execution, and client communication in Mannheim, Germany.
Regulatory CMC Manager supporting multi - product global regulatory CMC for products at Marketing Authorisation Application Stage. Focused on documentation preparation, submissions, and providing regulatory support.