Project Management Supervisor

For a leading Greek pharmaceutical company.

• →Lead and coordinate R&D projects, ensuring timely delivery within scope, budget, and quality requirements.
• →Collaborate with cross-functional teams (R&D, Regulatory Affairs, Supply Chain, Quality, and external partners) to support successful project execution.
• →Develop, monitor, and maintain project plans, timelines, milestones, and development trackers, proactively identifying risks and implementing corrective actions when needed.
• →Support the preparation, monitoring, and control of the R&D budget, ensuring alignment with financial targets and development priorities.
• →Coordinate interactions with external stakeholders, including API suppliers, CDMOs, CROs, and other development partners.
• →Monitor regulatory submission, dossier preparation, approval, and launch timelines to ensure projects progress according to plan.
• →Support portfolio evaluation activities by contributing to project feasibility assessments, development strategies, and business case analyses.
• →Coordinate intellectual property (IP) activities and patent-related assessments in collaboration with external patent advisors and internal teams.
• →Drive continuous improvement by implementing best practices and lessons learned across development projects.

• Bachelor’s degree in Pharmacy, Chemistry, Biology, Chemical Engineering, or a related scientific field.
• Minimum 2 years of experience in project coordination, project management, or a similar role within the pharmaceutical industry.
• Good understanding of pharmaceutical development processes and relevant regulatory requirements.
• Strong organizational, planning, and time management skills, with the ability to manage multiple projects and deadlines simultaneously.
• Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external stakeholders.
• Proficiency in Microsoft Office applications, particularly Excel and PowerPoint.
• Excellent command of the English language, both written and spoken.
• Experience in pharmaceutical product development, dossier submission processes, Bioequivalence studies, or technology transfer projects will be considered an asset.