Director of Supply Chain
- United States
- Permanent
- CAPEX Projects
This vacancy has now expired
Working alongside our client, a global innovator in Cell & Gene Therapy, as their newest Manufacturing Associate you will be responsible for providing support to CDMOs, particularly related to development and GMP manufacturing of gene-edited cell therapy drug products.
Led by mission-driven and visionary scientists, our client is truly passionate about their impact on the discoveries of cell gene and therapy. Your role here will make a difference to the world and is a contract you can be proud of.
Responsibilities:
- Develop a team of world class supply professionals focused on delivering for patients, working with integrity and collaborating effectively
- Define, execute and lead clinical supply and operations planning process (CS&OP), to ensure clinical demand, inventory, production, and budget are managed by an integrated operating plan.
- Ensure patient material chain of identity / chain of custody (COI/COC) is maintained at each stage of manufacture for client’s autologous cell therapy programs, in accordance with all industry regulations and SOPs.
- Establish cold chain shipping, distribution, and trade strategy and processes
- Qualify logistics providers and set up the supply chain including courier selection, container validation, etc.
- Own the relationship with qualified external supply chain partners.
- Manage all patient material & drug product shipping, labelling and distribution to worldwide clinical sites
- Coordinate shipments of in-process GMP materials and released clinical materials between vendors and storage sites
Experience, Education, Specialized Knowledge, and Skills:
- Must thrive in a fast-paced, growing, and innovative environment where flexibility, resourcefulness, resiliency, and communication skills are key. Excellent interpersonal skills, ability to develop important relationships with your stakeholders, and being an all around good company citizen are essential.
- BS or advanced degree in biology, chemistry, or engineering disciplines with a minimum of 8-10 years of relevant experience in biotech or pharmaceutical industries, ideally in a supply chain leadership role within the biotechnology or pharmaceutical industry;
- Experience with autologous cell therapy requirements (COC/COI) and/or ex-vivo gene therapy preferred.
- Leadership experience with clinical or commercial supply chain development, establishing short and long-range operational and strategic plans, and delivering results within tight project deadlines
- Demonstrated ability to manage supplier relationships for clinical manufacturing, including relationship building, improvement of execution deliverables and contract negotiation.
If this role is of interest to you, please apply now!
#LI-AN1
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
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