Job Description - Director/Senior Director, Supply Chain
Priovant
Therapeutics is committed to developing therapies that address high unmet needs in autoimmune diseases.
The Director/Senior
Director,
Supply Chain
will
further this mission by
ma
naging
worldwide
clinical distribution
for
our
late-stage
programs and
prepar
ing
the commercial supply chain
f
or
the
anticipated
launch
.
T
he successful candidate
will directly manage
packaging, labeling, and distribution
operations at external sites
,
and develop
commercial
distribution plans for our rare disease
portfolio.
The
Director/Senior
Director,
Supply Chain
reports
to the SVP, CMC. The position
is fully remote,
with
periodic
travel to meet with the team in the Durham, NC office required.
Responsibilities:
Oversee the clinical supply chain for solid oral and topical development programs and formulate commercial supply strategies that ensure readiness for product launch.
Directly manage packaging, labeling, and distribution at external manufacturing and logistics partners, driving engagement to meet overall program goals.
Work with the project team and external partners to establish and communicate aggressive but realistic timelines for drug availability.
React with adaptability and exhibit ownership in the face of timeline pressure and operational challenges.
Collaborate with commercial and regulatory partners to establish appropriate label content and packaging designs.
Work with the Chief Commercial Officer and other stakeholders to develop demand plans and an end-to-end commercial forecast for all manufacturing stages.
Manage drug movements and assist in understanding and fulfilling worldwide import requirements.
Contribute to commercial supply agreement negotiations.
Qualifications:
BS or BA degree in a scientific or business discipline, with at least 10 years of supply chain experience in the pharmaceutical industry.
Hands-on experience with commercial forecasting and inventory management, with commercial launch planning and execution experience strongly preferred.
Top-tier expertise in managing clinical supply chains, with a proven track record in working successfully with integrated CDMO partners.
Broad knowledge of logistical and regulatory considerations that may impact global movements of clinical and commercial supplies, including import licenses, shipping logistics, and customs clearance.
Experience in using and guiding configuration of IRT and ERP software.
Solid overall understanding of the development of oral dosage forms
,
pharmaceutical quality systems, and regulatory guidance
applicable to the manufacturing and labeling of finished drug
product
.
Ability to participate in complex commercial supply chain negotiations.
Desire
to contribute leadership, independent judgement, and an enthusiastic attitude to our fast-paced and dynamic environment.
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