PbALTEN Portugal /b, a leading force in the IT, Engineering and Life Sciences industries.
We are currently seeking a dedicated and detail-oriented bRegulatory Affairs Officer /b specialized in bArtwork Management /b /ppbr/ppbALTEN Group /b /ppWithin 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.
/ppbr/ppDo 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?
/ppAs a bRegulatory Affairs Officer /b, you will play a critical role in ensuring compliance with local and international regulatory standards across various markets.
/ppbr/ppbKey Responsibilities: /b /pullibArtwork Management: /b /liliReview and approve artwork to ensure compliance with regulatory standards and requirements.
/liliCoordinate with internal and external stakeholders, including design, marketing, and packaging teams, to ensure artwork is accurate and meets regulatory guidelines.
/liliEnsure timely updates of artwork to reflect any regulatory changes, including packaging and labelling components.
/lilibRegulatory Affairs Support: /b /liliAssist in the submission of regulatory dossiers, amendments, variations, and renewals for marketing authorizations.
/liliLiaise with health authorities and regulatory bodies, providing timely responses to regulatory queries and requests.
/li /ulpbQualifications: /b /pulliBachelor's degree in Life Sciences, Pharmacy, Regulatory Affairs, or a related field.
/lilibFluent in Nordic or Arabic or Turkish Languages, /b written and spoken (bMandatory) /b.
/liliPrevious experience in bRegulatory Affairs /b within the pharmaceutical industry, with a focus on bartwork management and labelling (preferred) /b /liliAttention to detail, with the ability to manage multiple tasks and projects simultaneously.
/liliExcellent communication and collaboration skills, with experience working in cross-functional teams.
/liliFamiliarity with software and tools related to artwork and labelling management is a plus.
/li /ulpbr/ppbLocation: /bFull Remote, Portugal.
/ppbr/ppbWhy Join Us?
/b /pulliPossibility to work with cutting-edge technology in the Life Sciences industry /liliCollaborative and dynamic work environment /liliPossibility to join a top-leading company in the industry /liliContinuous trainings /liliPossibility to join different and interesting projects /li /ulpbr/ppIf 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.
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