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Sr associate, manufacturing regulatory - temporary (12 months contract)

Pomezia
Contratto a tempo determinato
Altro
Pubblicato il 6 maggio
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OverviewThe Sr Associate, Manufacturing Regulatory Affairs is responsible for supporting regulatory activities within continuous improvement and compliance projects related to products, manufacturing, and analytical processes. The role ensures that all changes are assessed, documented, and managed in compliance with applicable regulatory requirements.

Job DescriptionRole PurposeThe Sr Associate, Manufacturing Regulatory Affairs is responsible for supporting regulatory activities within continuous improvement and compliance projects related to products, manufacturing, and analytical processes. The role ensures that all changes are assessed, documented, and managed in compliance with applicable regulatory requirements.

Key Responsibilities

Assess regulatory impact of changes related to manufacturing sites, processes, and products

Plan and support activities associated with CMC (Chemistry, Manufacturing & Controls) variations and manufacturing site changes

Coordinate the collection, review, and organization of GMP documentation required for regulatory submissions

Draft and review documentation supporting CMC variations and manufacturing changes

Prepare product-specific regulatory declarations and contribute to Product Quality Reviews (PQRs)

Collaborate cross-functionally with Quality, Manufacturing, and other relevant departments to ensure alignment on regulatory strategies and timelines

Support continuous improvement initiatives to ensure ongoing compliance with regulatory standards

QualificationsEducation

Degree in Pharmaceutical Chemistry and Technology (CTF), Chemistry, or Industrial Chemistry

A Master's degree in Regulatory Affairs is considered a strong asset

Experience

1–2 years of experience in Regulatory Affairs within pharmaceutical companies, preferably in an international environment

Skills & Competencies

Fluent in English (written and spoken)

Good proficiency with standard IT tools and basic statistical analysis

Strong attention to detail and quality-oriented mindset

Proactive, results-driven approach with the ability to manage assigned responsibilities independently

Excellent communication and interpersonal skills

Ability to work effectively in cross-functional teams

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