Manager Supply Chain Lead - Anderlecht, België - Pfizer

Pfizer
Pfizer
Geverifieerd bedrijf
Anderlecht, België

4 dagen geleden

Sophie Dubois

Geplaatst door:

Sophie Dubois

beBee Recruiter


Beschrijving

Do you want to be part of an international, innovative, world-class pharmaceutical company? Of an organization committed to putting patients first? Pfizer has always evolved with the changing needs of the people who rely on us to create a healthier world.


Guided by our four values:
Courage, Joy, Equity and Excellence, our breakthrough culture lends itself to our dedication to transforming millions of lives.


Location:
Belgium - Anderlecht

About the role


As a Supply Chain Lead, your advanced knowledge and solid understanding of clinical study design and drug supply processes, you will lead and manage matrix teams responsible for the end-to-end oversight of supply chain activities required for the provision of investigational product on phase I-IV protocols for both Small Molecule and Biologics programs.

Provide consult on all aspects of investigational product strategies and a key decision maker for the development of investigational product supply and sourcing strategies.

Responsible for designing strategies that align with program, protocol, and regulatory requirements, identifying and managing supply chain risk, managing multi-million clinical supply budgets, and providing guidance and leadership to the Clinical Supply Team.


Main responsibilities- Responsible for leading the development and execution of investigational and commercial material global supply strategies for early and late-stage development programs intended for regulatory approvals of new products, new indications, or line extensions of currently approved products.- Participate as a key member of the Pharmaceutical Sciences Project Team (PSPT) and Co-Development Team (CDT) to proactively recognize and address logístical and regulatory issues associated with the requirements of the clinical development program and project team objectives.- Participate as a core study team member to provide operational knowledge relating to Investigational Product (IP) and lead strategy discussions to align with protocol and operational needs for each study.

Proactively anticipate changes based on operational factors (countries, sites, enrollment), randomization configuration and protocol requirements- In partnership with the CST, develop clinical supply solutions, including packaging, blinding, and distribution strategies, that meet the needs of clinical studies as well as ensure patient compliance and safety.- Proactively identify risks and develop strategies to mitigate these risks and create contingency plans that minimize the impact of unanticipated events.- Manage clinical trial drug supply budget and communicate forecasts and changes effectively and in a timely fashion to study teams and GCS partner lines.- Ensure site and patient focus, along with quality compliance, throughout PharmSci and GCS processes.

Contribute to the investigation and implementation of corrective and preventative actions for Significant Quality Events (SQEs) and Good Manufacturing Practices (GMP) Incidents.

About you- B.S. degree (or equivalent) is required.

Advanced training in supply chain management, a scientific discipline, project management, or business administration is desirable.- Drug development, scientific research, or clinical study design including IRT, pharmaceutical manufacturing/packaging/labeling/distribution/Import export.- Management of multi-disciplinary teams that includes measuring work, negotiation, conflict management, process improvement, project management.- Proven ability to effectively develop, communicate, and gain support for execution plans with a wide range of stakeholders.- Experience managing change in a dynamic, complex environment.- Experience with budgeting and forecasting.

What do we offer?

Innovative company Pfizer has a pipeline full of innovative medicines for a variety of conditions.

As a Pfizer colleague, you'll have the opportunity to maximize the impact of medicines for patients in a variety of ways.

In short, you make a real difference.

Development opportunities We are always looking for top talent. We believe you will never stop learning and there will always be a new opportunity for your development. That is why we have broad opportunities in the Belux organization.

There are regular opportunities for training or to gain experience in a different field or even advancement to an international position.


A culture where you can be yourself We are a large, international organization with people from all over the world.

At Pfizer everyone should be able to be themselves, that's what we strive for and live by.


Work/life balance At Pfizer, we know that if you really want to make an impact on people's lives, it's important that your people are at their best.

That's why we offer our colleagues good working conditions, such as an appropriate salary and opportunities to work from home.

Working a lot of overtime is not the norm for us. We also believe that work and having fun should go hand in hand. That's why, for example, you can pa

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