Regulatory Affairs Specialist, Randstad

Randstad

Location:

Portugal, Lisboa

Category:

Research and Development

Contract Type:

Employment contract

Salary:

Not provided

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Job Description:

Responsible for preparing and submitting biocide and medical device registration dossiers meeting European requirements, interacting with stakeholders, and maintaining compliance with regulations.

Job Responsibility:

Maintaining company’s compliance with European chemicals legislation
Preparation and submission of registration dossiers under Biocidal Products Regulation
Interaction with external services providers for generation of tests and assessments
Interaction with authorities for submissions
Interaction with internal stakeholders and driving decision-making by proposing registration strategies
Providing guidance to R&D during new product development
Staying informed about national and European regulation developments
Participating in advocacy to influence regulatory developments.

Requirements:

A University Degree in Scientific background: Master or PhD, in Chemistry, Biochemistry, Toxicology. Ecotoxicology
3 to 5 of industry experience within Regulatory Affairs (registration, development, maintenance)
Experienced in Chemical Legislation, Chemical industry, Chemical Regulations (i.e. BPR, CLP, REACH, PPPR) & preparing regulatory dossiers
Proficiency in spoken and written English, knowledge of any other languages would be an asset
Project management skills, follow-through and hands on approach
Attention to detail and meeting deadlines
Analytical mind.

Nice to have:

Knowledge of any other languages
Advocacy experience via trade associations.

Additional Information:

Job Posted:

March 31, 2025

Expiration:

March 31, 2025

Employment Type:

Fulltime

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