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Job Requirements of Manager, Supply Planning:
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Employment Type:
Contractor
-
Location:
Boston, MA (Onsite)
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Manager, Supply Planning
Careers Integrated Resources Inc
Boston, MA (Onsite)
Contractor
Manager, Supply Planning
Location: Boston MA
Duration: 12 Months
Pay: $ 84.54- $99.46
POSITION SUMMARY
The Manager, Supply Planning is embedded within Client's External Manufacturing organization. This individual will own the end-to-end supply planning function for Verve Therapeutics' clinical programs, operating in a fully outsourced CDMO model built on mRNA/LNP technology. The role is foundational to the team's S&OP process design and will serve as the primary driver of 18-month rolling MRP for clinical drug product supply.
KEY RESPONSIBILITIES
Supply Planning & MRP
QUALIFICATIONS
Required
Location: Boston MA
Duration: 12 Months
Pay: $ 84.54- $99.46
POSITION SUMMARY
The Manager, Supply Planning is embedded within Client's External Manufacturing organization. This individual will own the end-to-end supply planning function for Verve Therapeutics' clinical programs, operating in a fully outsourced CDMO model built on mRNA/LNP technology. The role is foundational to the team's S&OP process design and will serve as the primary driver of 18-month rolling MRP for clinical drug product supply.
KEY RESPONSIBILITIES
Supply Planning & MRP
- Develop and maintain rolling supply plans for clinical drug product
- Generate forward-looking material requirements for drug substance intermediates and critical excipients
- Manage supply plan assumptions, risk scenarios, and inventory coverage targets in alignment with program timelines
- Build and maintain S&OP templates, KPIs, and reporting dashboards
- Prepare and present supply plan summaries for cross-functional leadership reviews
- Translate supply plans into manufacturing schedules coordinated across external CDMOs
- Monitor schedule adherence, batch release timelines, and supply risk through collaborative CDMO governance
- Maintain material genealogy and lot traceability across the multi-step supply chain
- Develop safety stock strategies for critical materials, accounting for CDMO lead times, shelf-life/expiry constraints, and clinical trial uncertainty
- Identify and escalate supply risks with mitigation options framed for leadership decision-making
- Support annual reportable change and regulatory change management (CMC) from a supply continuity standpoint
QUALIFICATIONS
Required
- Bachelor's degree in Supply Chain, Engineering, Life Sciences, or related field; advanced degree a plus
- 5+ years of supply chain or supply planning experience in pharmaceutical, biotech, or CDMO environment
- Hands-on experience with MRP/ERP systems (SAP strongly preferred)
- Direct experience with clinical supply planning in an outsourced manufacturing model
- Strong analytical skills; proficiency with supply planning tools and Excel/dashboard platforms
- Experience with advanced therapy or biologic modalities (LNP, mRNA, gene therapy, oligonucleoProduct)
- Familiarity with S&OP/IBP process design and implementation
- Exposure to CMC regulatory requirements (IND-stage) and supply risk classification
- APICS CPIM or CSCP certification
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