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LLOperational Readiness Technical Lead & Capital Projects Manager

Job in Redmond, King County, Washington, 98052, USA
Listing for: Veg Group
Full Time position
Listed on 2026-01-16
Job specializations:
  • Engineering
    Quality Engineering, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below
Position: LL01-260112 Operational Readiness Technical Lead & Capital Projects Manager

Career Opportunities with Validation & Engineering Group

A great place to work.

Current job opportunities are posted here as they become available.

LL01-260112 Operational Readiness Technical Lead & Capital Projects Manager

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas:
Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Operational Readiness Technical Lead & Capital Projects Manager

The Operational Readiness Technical Lead & Capital Projects Manager will lead a Manufacturing Expansion Project, drive increased manufacturing capacity and ensuring end-to-end readiness for GMP operations. This role is critical to expanding production capacity while maintaining full regulatory compliance and effective coordination with internal stakeholders, suppliers, and cross-functional teams.

The position provides technical leadership across project planning, design oversight, utilities integration, Commissioning & Qualification (C&Q), regulatory compliance, and operational readiness, applying lessons learned at startups to enable scalable, compliant manufacturing expansion.

Key Responsibilities
  • Project Planning & Coordination
  • Develop, maintain, and execute a comprehensive project plan covering all phases from design through Commissioning & Qualification (C&Q).
  • Define and manage milestones, schedules, dependencies, and deliverables.
  • Communicate project status, risks, and progress clearly to all stakeholders.
  • Ensure all design packages meet GMP requirements and align with operational readiness objectives.
  • Apply lessons learned from previous startups to improve design efficiency and scalability.
  • Support future expansion planning through robust, compliant design solutions.
  • Support installation and integration of critical utility systems.
  • Ensure utilities are designed, installed, and commissioned in compliance with GMP and regulatory standards.
  • Coordinate closely with engineering, construction, and vendors during execution.
  • Support development and execution of detailed C&Q plans for facilities, utilities, and manufacturing systems.
  • Ensure systems are validated, documented, and ready for operational use.
  • Align C&Q activities with quality and regulatory expectations.
  • Regulatory & GMP Compliance
  • Monitor and enforce compliance with cGMP, FDA, EMA, and applicable regulatory requirements.
  • Coordinate with Quality Assurance and Regulatory Affairs to ensure inspection readiness.
  • Ensure documentation supports regulatory submissions, audits, and inspections.
  • Identify, assess, and proactively mitigate project risks.
  • Maintain a comprehensive risk register with defined mitigation strategies.
  • Escalate critical risks and issues in a timely and structured manner.
  • Documentation & Reporting
  • Maintain complete and compliant project documentation, including:
  • Design reviews
  • Meeting minutes
  • Regulatory records
  • Lead weekly project and team meetings with clear agendas and actionable follow-ups.
  • Capital Projects Leadership Support
  • Partner with Capital Projects leadership to plan, execute, and close out site initiatives.
  • Ensure alignment with overall business, manufacturing, and operational strategy.
  • Knowledge Transfer & Team Integration
  • Provide mentorship, guidance, and training to project team members.
  • Ensure effective knowledge transfer to operations and site teams.
  • Support sustained operational readiness post-project handover.
Qualifications & Experience Required
  • Bachelor’s degree in Engineering or a related technical discipline.
  • Significant experience in GMP-regulated manufacturing environments (pharmaceutical, biotech, or medical device).
  • Proven experience managing capital projects, facility expansions, or manufacturing startups.
  • Strong working knowledge of:
  • GMP regulations
  • Utility systems
  • FDA and EMA regulatory frameworks
Preferred
  • Experience supporting manufacturing expansion or startup projects (IPOD, JPOD, or similar).
  • Strong cross-functional leadership and stakeholder management skills.
  • Experience working with Quality, Regulatory, Engineering, and Operations teams.
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