Hemofarm is a member of STADA Group, one of the largest global generic pharmaceutical companies, which successfully operates in both the markets of Serbia and Western Balkans. Hemofarm produces high quality pharmaceutical products within the leading pharmacotherapeutic groups, observing the key corporate values: Agility, Integrity, Entrepreneurship and ONE STADA. 

Coordinator Product Development Strategy & Project Management
Place of work: Belgrade/Vršac
Type of contract: Fix term - Maternity cover

About the job:

As a Coordinator Product Development Strategy & Project Management, you will lead and coordinate the project team and all phases of projects for the development of new or existing products, with the aim of creating a product aligned with the defined quality profile, budget, timelines, and its intended use. 

Responsibilities:

• Leading the development team that will define the product development plan, including technical, patent, clinical, and regulatory assessment
• Managing projects for the development of new or existing products with the aim of creating a product aligned with the defined quality profile, budget, timelines, and its intended use
• Developing technical expertise in all relevant areas of product development, such as formulation development, manufacturing process, packaging, analytical and stability development, as well as in key regulatory processes and documentation
• Reporting on project milestones, risks, budget, and other relevant project information
• Creating and reviewing project documentation related to pharmaceutical product development and relevant parts of the registration dossier
• Monitoring new professional and scientific literature
• Preparing budgets and managing costs related to development projects
• Drafting and reviewing local or global standard operating procedures and work instructions
• Ensuring compliance with standard operating procedures, including safety, GMP, and GCP requirements 

Qualifications:

• University degree in pharmacy, technology, or chemistry, with at least 3 years of work experience, preferably in the pharmaceutical industry, especially in product development, manufacturing, or quality, or experience in preparing the quality part of registration documentation
• Experience in leading teams, projects, and processes is a plus!
• High level of written and verbal communication in English language
• Strong technical background, as well as communication and organizational skills
• Advanced use of MS Office tools (Word, Excel, PowerPoint)
• This position requires coming to Vršac at least twice a week.

We offer: