Number of Applicants
:000+
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About PSC Biotech
Who are we?
PSC Biotech is a leading Biotech Consultancy firm founded
in 1996, headquartered in Pomona, California, USA, with Global operations in
Ireland, India, Singapore, Australia and the US, serving 350 clients in more
than 23 countries worldwide. We provide cloud -based software solutions for
Quality Management and Regulatory Inspections, pharmaceuticals contract
manufacturing professionals, and metrology services to our clients.
‘Take your Career to a new Level’
PSC Biotech disrupts the conventional consultancy model
by aligning our EVP as one of the unique selling point which includes the
opportunity to work with the most talented cohort of like -minded professionals
operating in the Pharma/ Biotech Industry. We offer a permanent contract of
employment giving exposure of working in Top Pharmaceutical client sites in a
diverse -cultural work setting.
Employee Value Proposition
Employees are the “heartbeat” of PSC Biotech, we provide
unparalleled empowering career development though Learning & Development
in -house training mentorship through constant guidance to facilitate career
progression. We believe in creating high performing teams that can exceed our
client’s expectations with regards to quality of all scalable and business unit
deliverables, staying under budget and ensuring timelines for our deliverables
are being met.
Overview:
The primary role of the Senior Material Planner is to
ensure the availability of raw material components to meet the production
schedule in Drug Substance, Drug Product and Finish Goods Packaging Operations.
Ensure raw material components are planned, purchased and released within the
guidelines established in the ERP SAP system. The Senior Material Planner will
play a key role in the ensuring that the functional goals are met. This will
require supporting the development and implementation of systems, processes and
people to ensure optimal raw material coverage in line with the Master
Production Schedule as well as product launch activities.
Technical Operations group is responsible for creating
our drugs for use in clinical trials and for scaling production of those drugs
for the commercial market. These individuals build and maintain cutting -edge
manufacturing processes and sites, provide quality assurance and quality
control to ensure we meet regulatory standards, and procure the needed goods
and services to support manufacturing and coordinating the worldwide movement
of our drugs to patients.
Key Responsibilities:
Knowledge, Skills and Capabilities:
Experience:
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