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Jobs at Viridian Therapeutics, Inc

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Director, Manufacturing Supply Chain Operations

  • Viridian Therapeutics, Inc

    • On-site
    • Waltham, MA

Senior Director, Medical Director

  • Viridian Therapeutics, Inc

    • On-site
    • Waltham, MA

Associate Director, Accounting

  • Viridian Therapeutics, Inc

    • On-site
    • Waltham, MA

Associate Director, Quantitative System Pharmacology

  • Viridian Therapeutics, Inc

    • On-site
    • Waltham, MA

Medical Director, Pharmacovigilance

  • Viridian Therapeutics, Inc

    • On-site
    • Waltham, MA

Analyst, Compliance

  • Viridian Therapeutics, Inc

    • On-site
    • Waltham, MA

Senior Director, Pricing & Contracting

  • Viridian Therapeutics, Inc

    • Remote
    • Massachusetts

Manager Quality Compliance

  • Viridian Therapeutics, Inc

    • On-site
    • Waltham, MA

Senior Manager, R&D Quality

  • Viridian Therapeutics, Inc

    • On-site
    • Waltham, MA

Associate Director, G&A Applications

  • Viridian Therapeutics, Inc

    • On-site
    • Waltham, MA

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Director, Manufacturing Supply Chain Operations

  • Viridian Therapeutics, Inc

  • Waltham, MA 02451
Open in New Tab

On-site

Not Disclosed

Bio-Pharma

Manufacturing+1

  • Posted on:

Job Description

Summary

Reporting to the Vice President, External Manufacturing & Supply Chain, the Director, Manufacturing & Supply Operations will lead business operations activities that support Technical Operations, including contract negotiation and lifecycle management, budget planning and roll-up, and business reviews. Operating with significant autonomy, this individual contributor role will impact through matrix leadership, vendor and stakeholder influence, and ownership of business processes that support program, financial, and operational decision-making across Technical Operations.

Responsibilities
  • Provide matrix leadership by influencing internal stakeholders, external vendors, and cross-functional partners to align operational decision-making by translating program priorities, business planning, financial assumptions, risk trade-offs, and decision-making inputs without direct people management authority.
  • Lead contract planning, negotiation support, execution, and lifecycle management for Technical Operations
  • Partner with Legal, Finance, and functional stakeholders to ensure contracts include appropriate business terms, deliverables, governance expectations, performance metrics, budget assumptions, and compliance requirements
  • Build productive relationships with external partners and internal stakeholders to support effective negotiation, clear accountability, timely execution, and practical resolution of business and operational issues
  • Contribute to Technical Operations budget management processes, including annual planning inputs, forecast updates, purchase order oversight, invoice review, accrual support, variance analysis, and consolidated budget roll-ups for leadership review
  • Orchestrate governance meetings and business reviews, ensuring clear agendas, decision logs, action tracking, risk escalation, and follow-through on commitments across internal and external stakeholders
  • Support vendor selection, onboarding, and transition activities by coordinating business requirements, operational assumptions, proposal comparisons, contracting needs, budget impacts, governance expectations, and stakeholder decision-making inputs
  • Identify opportunities to improve vendor value, operating efficiency, cost management, contract structure, governance discipline, and cross-functional ways of working across the Technical Operations supplier network


Qualifications
  • Requires 12+ years of progressive biotechnology or pharmaceutical experience, including substantial experience manufacturing and supply chain, and related GMP operations
  • Bachelor’s degree in Supply Chain Management, Life Sciences, Pharmacy, Engineering, or a related discipline required
  • Demonstrated Director-level ability to participate with senior management in establishing strategic plans and objectives, translate functional strategy into operational plans, and ensure effective execution across internal teams and external partners
  • Mastery of the core functional area with strong understanding of how Supply Chain, External Manufacturing, CMC, Quality, and Regulatory intersect to support company goals and competitive positioning
  • Proven ability to resolve complex, cross-functional operational issues where problems are not clearly defined; anticipates risks, develops practical mitigation plans, and drives measurable outcomes
  • Demonstrated success leading through influence in matrixed environments, including aligning senior stakeholders, reconciling multiple perspectives, and negotiating matters of significance with vendors, partners, or major customers without reliance on direct reporting authority
  • Demonstrated knowledge of contract management, budgeting processes, supplier governance, business reviews, KPIs, and issue escalation
  • Combination drug-device experience desirable
  • Strong written, verbal, and executive-level communication skills; able to operate with significant autonomy, sound judgment, and high accountability in a fast-paced matrix environment
  • Ability to travel domestically and internationally, as needed
  • The salary range for this position is commensurate with experience

 

Education

Degree

Bachelor

Specialization

Supply Chain Management/Life Sciences/Pharmacy/Engineering
Experience:

13-16 yrs

  • Skills:
  • Biopharmaceutical Supply Chain
  • Manufacturing Operations
  • External Manufacturing Finance handling
  • CMO / CDMO Management
  • Supply & Demand Planning
  • Supplier Governance
  • KPI Management
  • Risk Management
  • Job Type:
  • Full-time
  • Shift Type:
  • Day shift
  • Monday to Friday
  • 8 hour shift

Compensation

  • Benefits:
  • 401K
  • 401K Match
  • Medical, Dental, Vision
  • Additional:
  • Base Salary

Job ID:

CGXP_26_19625

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