Hemofarm is a member of STADA group, one of the largest global pharmaceutical companies, that successfully operates in Serbian and West Balkan markets. Hemofarm manufactures high quality pharmaceutical products within the leading pharmacotherapeutic groups, complying with core corporate values: Agility, Integrity, Entrepreneurship and ONE STADA. 

Product development project manager/associate
Job location: Vršac, Belgrade

Job requirements:
•    University degree in pharmacy, technology, or chemistry.
•    Experience of at least 7 years in pharmaceutical development or manufacturing, notably managing introduction or transfers of new or existing technologies and/or products, as well as experience in the preparation of the quality part of registration documentation.
•    Experience in leading teams and managing of projects (advantage ASQ GB or PMP certification).
•    Proficient in English (written and spoken).
•    Strong technical background, along with communication and organizational skills.
•    Advanced use of MS Office tools (Word, Excel, Power Point).

Key responsibilities:
•    Leads the new product development projects aiming to create a product compliant with the defined target profile and its intended use.
•    Ensures elaboration of project development plan including risk management. Ensures that all required tasks and actions are completed at all project stages to achieve desired results. 
•    Provides guidance and mentoring to the pharmaceutical development and other team members towards the smooth project execution. Applies knowledge and directs experience to ensure appropriate methodologies are in place and fit-for-purpose to properly support the development projects.
•    Facilitates the execution of development projects by working collaboratively with the other global and local functions and takes care that project targets and strategy is easily understood by all relevant stakeholders.
•    Provides reporting on project milestones, risks, and budget. Communicate complex technical issues and deliver clear and concise presentations to management and non-technical stakeholders.
•    Provides approval of all project related pharmaceutical development and regulatory documentation.
•    Participates in creation of own patent applications and scientific articles, when required.

Additional benefits:
•    Work within dynamic, cross functional, global team.
•    Continuous education and learning.
•    Opportunities for growth and development.
•    Private health insurance