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Senior Material Excellence Engineer, Site MSAT

Infobahn Softworld Inc.

Raritan, New Jersey • Today

Easy Apply

Full-time, Contract, Third Party

Job Details

Skills

Innovation
Sustainability
Process Optimization
Sourcing
Boost
Project Governance
Logistics
Manufacturing Operations
Risk Management
Risk Assessment
Supply Chain Management
Dashboard
Analytics
Collaboration
Leadership
Quality Assurance
Biochemistry
Chemical Engineering
Life Sciences
Pharmaceutics
Biotechnology
Good Manufacturing Practice
Change Control
URS
Material Characterization
Manufacturing
Workflow
Microsoft Excel
Microsoft PowerPoint
PMP
Critical Path Method
Project Management

Innovation
Sustainability
Process Optimization
Sourcing
Boost
Project Governance
Logistics
Manufacturing Operations
Risk Management
Risk Assessment
Supply Chain Management
Dashboard
Analytics
Collaboration
Leadership
Quality Assurance
Biochemistry
Chemical Engineering
Life Sciences
Pharmaceutics
Biotechnology
Good Manufacturing Practice
Change Control
URS
Material Characterization
Manufacturing
Workflow
Microsoft Excel
Microsoft PowerPoint
PMP
Critical Path Method
Project Management

Summary

Job Title: Senior Material Excellence Engineer, Site MSAT

Location: Raritan, NJ

12+ Months Contract

Position Summary:

The Senior Material Excellence Engineer, Site MSAT will lead global implementation initiatives for the dual sourcing of Lentivirus (LV) materials under Project S.U.R.G.E (Single Use Resiliency & Growth Evolution). This role drives operational reliability, innovation, and sustainability across internal and external global manufacturing facilities. Operating within a cross-functional and global matrix setting, this role requires strong project management capabilities, regulatory change-control expertise, and deep technical knowledge of pharmaceutical/biotech manufacturing processes related to viral vectors and cell therapies.

Key Responsibilities:

Dual Sourcing & Process Optimization: Identify, scope, and lead dual-sourcing projects for critical single-use and raw materials utilized in lentivirus manufacturing to boost plant reliability and supply security.
Technical Vendor Execution: Author User Requirement Specifications (URS), perform technical reviews of vendor engineering drawings, execute formal material comparability assessments, define critical material attributes, and initiate/close change controls.
Project Governance: Build and maintain detailed schedules using MS Project, tracking critical path items, handoffs, key milestones, and high-level deliverables.
Supply Chain & Manufacturing Alignment: Partner closely with production, supply chain, logistics, and MSAT teams to ensure material changes integrate smoothly without disrupting manufacturing operations.
Risk Management & Analytics: Conduct structured risk assessments to proactively mitigate supply chain and manufacturing vulnerabilities; develop executive visuals, dashboards, and timeline analytics.
Cross-Functional Collaboration: Act as the primary technical MSAT liaison across site leadership, global matrix teams, external suppliers, and quality assurance.

Qualifications & Requirements:

Education: Bachelor's degree in Biotechnology, Biochemistry, Chemical Engineering, or a related life sciences discipline.
Experience:
- Minimum 5+ years of hands-on experience in the pharmaceutical or biotechnology sector.
- At least 3+ years of formal project management experience within a technical/manufacturing setting.
- Prior experience with lentiviral vectors (LVV), viral manufacturing, single-use technologies (SUT), or cell & gene therapies is strongly preferred.
Technical & Regulatory Competencies:
- Solid working knowledge of cGMP guidelines, FDA, and EMA regulatory standards.
- Experience with change control procedures, URS generation, material characterization, and tech transfers.
- Background in upstream and downstream biologics manufacturing workflows.
Tools & Software:
- Advanced proficiency with MS Project, Excel, and PowerPoint.
- PMP, CPM, or equivalent project management certification is a plus.

Thanks

Sri Vardhan

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: infobahn
Position Id: 2026-63058
Posted 14 days ago

Fitment

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Job Details

Skills

Innovation
Sustainability
Process Optimization
Sourcing
Boost
Project Governance
Logistics
Manufacturing Operations
Risk Management
Risk Assessment
Supply Chain Management
Dashboard
Analytics
Collaboration
Leadership
Quality Assurance
Biochemistry
Chemical Engineering
Life Sciences
Pharmaceutics
Biotechnology
Good Manufacturing Practice
Change Control
URS
Material Characterization
Manufacturing
Workflow
Microsoft Excel
Microsoft PowerPoint
PMP
Critical Path Method
Project Management

Innovation
Sustainability
Process Optimization
Sourcing
Boost
Project Governance
Logistics
Manufacturing Operations
Risk Management
Risk Assessment
Supply Chain Management
Dashboard
Analytics
Collaboration
Leadership
Quality Assurance
Biochemistry
Chemical Engineering
Life Sciences
Pharmaceutics
Biotechnology
Good Manufacturing Practice
Change Control
URS
Material Characterization
Manufacturing
Workflow
Microsoft Excel
Microsoft PowerPoint
PMP
Critical Path Method
Project Management

Summary

Job Title: Senior Material Excellence Engineer, Site MSAT

Location: Raritan, NJ

12+ Months Contract

Position Summary:

Key Responsibilities:

Dual Sourcing & Process Optimization: Identify, scope, and lead dual-sourcing projects for critical single-use and raw materials utilized in lentivirus manufacturing to boost plant reliability and supply security.
Technical Vendor Execution: Author User Requirement Specifications (URS), perform technical reviews of vendor engineering drawings, execute formal material comparability assessments, define critical material attributes, and initiate/close change controls.
Project Governance: Build and maintain detailed schedules using MS Project, tracking critical path items, handoffs, key milestones, and high-level deliverables.
Supply Chain & Manufacturing Alignment: Partner closely with production, supply chain, logistics, and MSAT teams to ensure material changes integrate smoothly without disrupting manufacturing operations.
Risk Management & Analytics: Conduct structured risk assessments to proactively mitigate supply chain and manufacturing vulnerabilities; develop executive visuals, dashboards, and timeline analytics.
Cross-Functional Collaboration: Act as the primary technical MSAT liaison across site leadership, global matrix teams, external suppliers, and quality assurance.

Qualifications & Requirements:

Education: Bachelor's degree in Biotechnology, Biochemistry, Chemical Engineering, or a related life sciences discipline.
Experience:
- Minimum 5+ years of hands-on experience in the pharmaceutical or biotechnology sector.
- At least 3+ years of formal project management experience within a technical/manufacturing setting.
- Prior experience with lentiviral vectors (LVV), viral manufacturing, single-use technologies (SUT), or cell & gene therapies is strongly preferred.
Technical & Regulatory Competencies:
- Solid working knowledge of cGMP guidelines, FDA, and EMA regulatory standards.
- Experience with change control procedures, URS generation, material characterization, and tech transfers.
- Background in upstream and downstream biologics manufacturing workflows.
Tools & Software:
- Advanced proficiency with MS Project, Excel, and PowerPoint.
- PMP, CPM, or equivalent project management certification is a plus.

Thanks

Sri Vardhan

Dice Id: infobahn
Position Id: 2026-63058
Posted 14 days ago

Fitment

Dice Job Match Score™

To see how well you match this job, please log in or create an account.

Once logged in, be sure to complete your profile to get the most accurate match score.

Create job alert

Never miss an opportunity! Create an alert based on the job you applied for.

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•

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•

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