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.
Design & Engineering Oversight
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.
Utilities Installation & Integration
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.
Commissioning & Qualification (C&Q) Readiness
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.
Risk Management
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
Status reports
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.
Support continuous improvement across capital delivery processes.
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:
Bachelors 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
Commissioning & Qualification (C&Q)
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.
Key Competencies
Operational readiness leadership
Capital project execution
GMP and regulatory compliance
Risk management and issue resolution
Clear communication and documentation
Team leadership and knowledge transfer
Required Experience:
Manager
Validation & Engineering Group Proudly serving our clients since 1997 Validation & Engineering Group provides world-class service and expertise to the Biotechnology, Food Safety and Quality, Medical Devices, and Pharmaceutical Industries. We offer our clients: Validation, Control Syst ... View more