#PolpharmaBiologics is a state-of-the-art biological R&D and manufacturing facility, one of the most modern in Europe. We have a fantastic, international team of experienced experts and dynamic young scientists with common goals and values. Biotechnology is our passion. Together we develop medicine, offering new hope to patients suffering from serious diseases.
We create a passionate and friendly workplace environment. Join us!
- International work environment
- Attractive salary
- Cutting-edge technology equipment
- Conferences and trainings around the world
In this role your focus will be on optimizing future success of Polpharma Biologics programs by defining scientifically sound and well thought-through development strategies. You will manage all non-technical aspects of a biosimilar development or CDMO program according to agreed timelines and budget, and provide scientific / strategic leadership of project teams
- Developing commercial target product profile including device and diagnostic needs as appropriate
- Leading project team working collaboratively with functional team members (technical, clinical, regulatory, commercial, IP)
- Holding overarching budget responsibility and presenting clearly why changes occur
- Managing the process of building strategic and operational development plans for respective program with the objective to optimize value, time, resources and risks
- Leading scenario generation, contingency planning, conflict resolution and the process of decision-making within the team
- Driving team members to create thoroughly evaluated recommendations for decision-making
- Drawing the clear thread between functional departments to be able to provide a distinct understanding of the implications of topics across departments
- Serving as the interface to all non-technical aspects of the program to senior management and the partner as applicable
- Documenting team meetings and report at PDRMs, PUMs and other meetings as necessary
- Developing strong relationships with internal stakeholders and CDMO clients or partners
- Providing clear and fast communication to partner as applicable
- Utilizing project management tools to enable clear dashboard reporting on program
- Taking accountability for executing the program in time, quality, and cost
- Ensuring continuous close alignment with the respective technical program manager for the same program as applicable
- At least 7 years’ experience in the pharmaceutical industry at least some of which must have been working with biologics and biosimilars
- Certification in project management (PMP, CAPM or equivalent) is preferred
- Excellent knowledge of pre-clinical, clinical development and regulatory processes
- Good understanding of pharmaceutical markets and competitive environment
- Experience in project management and member of a cross-functional project team
- Good knowledge of MS Office and MS Project is required
- Excellent oral and written communication skills including senior management focus
- Fluency in English
- Highly customer-oriented mindset, friendly and easy to work with attitude
- High degree of self-awareness
- Advanced planning skills and expert skills to facilitate / optimize contribution of team members as individuals and members of a cohesive team
- Ability to prioritize and deliver against timelines
- Strong leadership and expert team management skills
- Orientation towards collaboration and aligned decision-making
- Ability to influence and drive decisions forward
- High degree of self-awareness
- Advanced planning skills and expert skills to facilitate / optimize contribution of team members as individuals and members of a cohesive team
- Ability to prioritize and deliver against timelines
- Strong leadership and expert team management skills
- Orientation towards collaboration and aligned decision-making
- Ability to influence and drive decisions forward
- Sport Card
- Development programs
- Private healtcare
- Relocation package
- Fruit day
- Integrations events
- Benefit platform
- and more
Aleksandra Bufnal
aleksandra.bufnal@PolpharmaBiologics.com
Poznaj
Rezon Bio
Dołącz do zespołu ponad 1300 specjalistów produkujących zaawansowane leki biologiczne, które poprawiają jakość życia pacjentów na całym świecie.
Bazując na doświadczeniu Polpharma Biologics, Rezon Bio działa jako partner CDMO (Contract Development and Manufacturing Organization).
Dzięki nowoczesnym centrom biotechnologicznym w Gdańsku i Warszawie-Duchnicach oferujemy szeroki wachlarz możliwości karierowych w obszarach naukowych, technicznych i biznesowych.