ALTEN Portugal, a leading force in the IT, Engineering and Life Sciences industries. We are currently seeking a dedicated and detail-oriented Regulatory Affairs Officer specialized in Artwork Management and Labelling. ALTEN Group Within 30 years, ALTEN has become leader in both outsourced Engineering and IT Enterprise Services. ALTEN, composed of 54,000 employees (88% engineers), carries out complex and highly technical projects throughout the value chain of 6,500 clients, the most prestigious companies in all sectors of industry, services and telecommunications. We work with key actors in the Aeronautics & Space, Defense & Naval, Security, Automotive, Rail, Energy, Life Sciences, Finance, Retail, Telecommunications and Services sectors.
Do you want to work in exciting projects at renowned clients? At ALTEN we believe that knowing and meeting the expectations of our consultants is a key factor in our success. Our consultants make the difference. Do you want to make the difference too?
As a Regulatory Affairs Officer, you will play a critical role in ensuring compliance with local and international regulatory standards across various markets.
Key Responsibilities: Artwork Management: Review and approve artwork to ensure compliance with regulatory standards and requirements.Coordinate with internal and external stakeholders, including design, marketing, and packaging teams, to ensure artwork is accurate and meets regulatory guidelines.Ensure timely updates of artwork to reflect any regulatory changes, including packaging and labelling components. Labelling Compliance: Prepare, review, and update product labels in compliance with country-specific regulations.Translate and localize product labels and packaging content, ensuring accuracy and compliance with local regulatory requirements.Collaborate with cross-functional teams to ensure labelling updates are implemented effectively and on time. Regulatory Affairs Support: Monitor regulatory changes and updates in relevant markets, ensuring the company is compliant with local and international regulatory frameworks.Assist in the submission of regulatory dossiers, amendments, variations, and renewals for marketing authorizations.Liaise with health authorities and regulatory bodies, providing timely responses to regulatory queries and requests. Qualifications: Bachelor's degree in Life Sciences, Pharmacy, Regulatory Affairs, or a related field.Previous experience in Regulatory Affairs within the pharmaceutical industry, with a focus on artwork management and labelling.Strong understanding of regulatory requirements for pharmaceutical products.Attention to detail, with the ability to manage multiple tasks and projects simultaneously.Excellent communication and collaboration skills, with experience working in cross-functional teams.Familiarity with software and tools related to artwork and labelling management is a plus. Location: Full Remote, Portugal.
Why Join Us? Possibility to work with cutting-edge technology in the Life Sciences industryCollaborative and dynamic work environmentPossibility to join a top-leading company in the industryContinuous trainingsPossibility to join different and interesting projects If you want to embrace in a new and challenging opportunity and are excited about the opportunity to contribute to our team, we want to hear from you! Please submit your resume and cover letter detailing your relevant experience and qualifications.