Process Engineer
Listed on 2026-10-11
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Manufacturing / Production
Quality Engineering, Manufacturing Engineer
Source One is a consulting services company and we’re currently looking for the following individual to work as a consultant with our direct client, a global pharmaceutical manufacturing client in Raritan, NJ.
No Third-Party, No Corp to Corp, No Sponsorship Now, Future or Current Temporary Authorization
Title:Process Engineer (MSAT) Location Raritan, NJ Onsite (Mon-Fri, 40 hours) Contract Duration: 12 months, with likely extension Pay Rate: $51.48 per hour (w2)
Position Overview
We are seeking a Senior Material Excellence Engineer, Site MSAT to lead the
global implementation of dual sourcing strategies for lentiviral materials as part
of Project S.U.R.G.E. (Single Use Resiliency & Growth Evolution). This role will
help strengthen manufacturing reliability, innovation, sustainability, and
process robustness across global sites and manufacturing operations. The
position will work closely with cross functional teams, site and global leadership,
manufacturing organizations, suppliers, and external partners to successfully
execute critical material and process initiatives.
The ideal candidate brings strong project management capabilities, technical
knowledge of biological manufacturing, and the ability to operate effectively in
a complex global matrix environment. Experience with viral manufacturing,
lentiviral vectors, cellular therapies, or other advanced therapies is highly
Key ResponsibilitiesLead process improvement initiatives focused on the dual sourcing of
materials used in lentiviral manufacturing to improve reliability, resiliency,
process performance, and operational effectiveness.
Develop and manage detailed project plans for dual sourcing initiatives
under Project S.U.R.G.E., including timelines, deliverables, milestones,
risks, and cross functional dependencies.
Lead activities related to vendor and material identification, including
identifying materials for dual sourcing, developing User Requirements
Specifications, reviewing and approving vendor drawings, conducting
formal comparability assessments, defining material quality attributes,
and creating and implementing change controls.
Support the development and implementation of standard processes for
supply chain management, logistics, and distribution to improve
operational effectiveness.
Partner with production and manufacturing teams to optimize resources,
improve manufacturing performance, reduce costs, and strengthen
process robustness.
Drive organizational change through effective project management,
stakeholder engagement, and communication strategies.
Coordinate team activities, delegate responsibilities, and provide clear
direction to support successful project execution.
Monitor and analyze manufacturing performance and identify
opportunities for process improvement, cost reduction, increased
reliability, and operational excellence.
Conduct risk assessments and develop mitigation strategies to address
technical, operational, and project risks.
Create clear visuals, analytics, and project reporting to communicate
critical paths, key handoffs and transitions, milestones, and high level
Collaboration and CommunicationCollaborate with local and global stakeholders across MSAT,
manufacturing, production, supply chain, quality, project teams, and
leadership organizations.
Represent Site MSAT in internal and external meetings and communicate
manufacturing requirements, technical considerations, project status, and
key insights.
Build effective relationships with internal and external partners and
facilitate alignment across a global organization.
Required QualificationsBachelor’s degree in Biochemistry, Biotechnology, Chemical Engineering,
or a related scientific or engineering discipline.
Approximately 5 years of experience in the pharmaceutical or
biotechnology…
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