{"id":2344,"date":"2025-07-14T11:16:56","date_gmt":"2025-07-14T11:16:56","guid":{"rendered":"https:\/\/strategicpartners.gr\/?post_type=awsm_job_openings&p=2344"},"modified":"2025-07-14T11:16:57","modified_gmt":"2025-07-14T11:16:57","slug":"regulatory-affairs-manager","status":"publish","type":"awsm_job_openings","link":"https:\/\/strategicpartners.gr\/index.php\/jobs\/regulatory-affairs-manager\/","title":{"rendered":"Regulatory Affairs Manager"},"content":{"rendered":"\n

Are you passionate about regulatory strategy and ready to play a central role in shaping the future of pharmaceutical development? A growing and innovation-driven pharmaceutical company is seeking a skilled and proactive Regulatory Affairs Manager<\/strong> to lead the preparation and coordination of regulatory activities across its expanding product portfolio.<\/p>\n\n\n\n

This position offers the opportunity to work in a collaborative environment with a strong pipeline of therapeutic solutions. You will be responsible for driving regulatory excellence and supporting product lifecycle management with strategic insight.<\/p>\n\n\n\n

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Main Responsibilities<\/strong><\/h3>\n\n\n\n
    \n
  • Provide expert regulatory input and compile key elements of regulatory submissions, including Modules 1, 2, and 3 of the Common Technical Document (CTD).<\/li>\n\n\n\n
  • Coordinate the preparation and timely submission of regulatory applications in compliance with applicable EU legislation and guidelines.<\/li>\n\n\n\n
  • Serve as the primary liaison with health authorities, managing communication, responding to questions, and facilitating the process of scientific advice.<\/li>\n\n\n\n
  • Contribute to regulatory strategy during product development and post-marketing phases, aligning regulatory objectives with overall business goals.<\/li>\n\n\n\n
  • Build and maintain productive relationships with regulatory bodies to ensure efficient review and approval processes.<\/li>\n<\/ul>\n\n\n\n
    \n\n\n\n

    Candidate Profile<\/strong><\/h3>\n\n\n\n

    Required Qualifications<\/strong><\/h4>\n\n\n\n
      \n
    • Bachelor\u2019s degree in Pharmacy, Chemistry, Biology, or a related life science discipline.<\/li>\n\n\n\n
    • A Master\u2019s degree in Pharmaceutical Sciences, Regulatory Affairs, or Industrial Pharmacy will be considered a strong asset.<\/li>\n<\/ul>\n\n\n\n

      Professional Experience<\/strong><\/h4>\n\n\n\n
        \n
      • Minimum of 3 years’ experience in Regulatory Affairs, with proven expertise in EU regulatory submissions and procedures.<\/li>\n\n\n\n
      • Familiarity with the preparation of full CTD dossiers and the regulatory lifecycle of pharmaceutical products.<\/li>\n<\/ul>\n\n\n\n

        Key Competencies<\/strong><\/h4>\n\n\n\n
          \n
        • Excellent command of both Greek and English (written and spoken).<\/li>\n\n\n\n
        • Strong communication and interpersonal skills with the ability to interpret and clearly present regulatory and scientific information.<\/li>\n\n\n\n
        • Highly organized, with the ability to manage multiple tasks and meet tight deadlines.<\/li>\n<\/ul>\n\n\n\n
          \n\n\n\n

          \u00a0Why Apply<\/strong><\/h3>\n\n\n\n

          This is a unique opportunity to take ownership of regulatory pathways for innovative products and make a meaningful impact on patient access to high-quality therapies. You will join a passionate team committed to scientific excellence and regulatory compliance in a fast-evolving industry.<\/p>\n\n\n\n

          What’s Offered<\/strong><\/p>\n\n\n\n

            \n
          • Gross monthly salary of \u20ac3,000<\/strong><\/li>\n\n\n\n
          • Private health insurance<\/strong><\/li>\n\n\n\n
          • Meal vouchers \/ Subsidized lunch allowance<\/strong><\/li>\n\n\n\n
          • Exposure to innovative, international R&D projects in the generic and value-added space<\/li>\n\n\n\n
          • Collaborative, science-driven environment with growth potential<\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"

            Are you passionate about regulatory strategy and ready to play a central role in shaping the future of pharmaceutical development? A growing and innovation-driven pharmaceutical company is seeking a skilled and proactive Regulatory Affairs Manager to lead the preparation and coordination of regulatory activities across its expanding product portfolio. This position offers the opportunity to work in<\/p>\n","protected":false},"author":1,"template":"","meta":{"content-type":"","inline_featured_image":false},"class_list":["post-2344","awsm_job_openings","type-awsm_job_openings","status-publish","hentry","job-type-on-site","job-location-athens"],"_links":{"self":[{"href":"https:\/\/strategicpartners.gr\/index.php\/wp-json\/wp\/v2\/awsm_job_openings\/2344","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/strategicpartners.gr\/index.php\/wp-json\/wp\/v2\/awsm_job_openings"}],"about":[{"href":"https:\/\/strategicpartners.gr\/index.php\/wp-json\/wp\/v2\/types\/awsm_job_openings"}],"author":[{"embeddable":true,"href":"https:\/\/strategicpartners.gr\/index.php\/wp-json\/wp\/v2\/users\/1"}],"wp:attachment":[{"href":"https:\/\/strategicpartners.gr\/index.php\/wp-json\/wp\/v2\/media?parent=2344"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}