Senior Capital Projects Leader – Pharmaceutical Manufacturing

Kindeva; Bridgeton (MO); On-site; USD 120,000 - 180,000; Full time

Benefits offered by this job

Competitive base salary

Performance bonus

Comprehensive benefits package (health

Vision

401k

Mentorship and development

Job summary

Kindeva is seeking a Senior Capital Project Engineer to lead major capital initiatives across manufacturing, facilities, utilities, quality, and growth objectives. You will partner with Operations, Validation, Engineering, and Finance to deliver projects safely, on schedule, and within budget.

The role emphasizes technical depth, business acumen, and the ability to influence stakeholders at all levels. On-site collaboration and a focus on GMP compliance are required.

Qualifications

• Bachelor's degree in Mechanical, Chemical, Electrical, Industrial, Civil, or related Engineering discipline.
• 8+ years of progressive engineering and capital project management experience.
• Experience managing large-scale capital projects and multi-million-dollar capital investments.
• Experience in pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.
• Experience leading projects in pharmaceutical drug product manufacturing.
• Experience supporting sterile fill finish, aseptic manufacturing, visual inspection, packaging, or device manufacturing operations.
• Demonstrated success leading capital projects from concept through startup and closeout.
• Experience managing project budgets, forecasts, and financial performance.
• Experience leading cross-functional teams and managing external contractors.
• Strong communication, leadership, problem-solving, and stakeholder management skills.
• Ability to influence decisions and drive alignment across all levels of the organization.

Responsibilities

• Lead complex capital projects from concept through startup, including scope development, project justification, engineering design, procurement, construction, commissioning, and operational handoff.
• Develop project business cases, capital requests, budgets, schedules, and funding strategies while maintaining accountability for project cost, cash flow, and overall financial performance.
• Partner with Operations, Quality, Validation, Engineering, Maintenance, Supply Chain, and Facilities teams to deliver projects that support business objectives while minimizing operational disruption.
• Manage engineering firms, contractors, equipment suppliers, and consultants to ensure safe, compliant, and effective project execution.
• Evaluate technical alternatives and provide recommendations that balance safety, quality, operational requirements, cost, schedule, and long-term business needs.
• Present project proposals, investment recommendations, project status, risks, and mitigation plans to site and executive leadership.
• Ensure projects are executed in compliance with applicable safety, GMP, regulatory, and company standards, including support of commissioning, qualification, and validation activities as required.
• Identify and mitigate project risks while driving timely resolution of technical, operational, financial, and schedule-related issues.
• Mentor and provide technical guidance to project team members while supporting continuous improvement of capital planning, project delivery, and engineering processes.

Skills

Project leadership

Cross-functional collaboration

Stakeholder management

Regulatory compliance

Cost control & budgeting

Risk assessment

Education

Bachelor's degree in Mechanical, Chemical, Electrical, Industrial, Civil, or related Engineering discipline

Job description

Kindeva is seeking a Senior Capital Project Engineer to lead major capital initiatives across manufacturing, facilities, utilities, quality, and growth objectives. You will partner with Operations, Validation, Engineering, and Finance to deliver projects safely, on schedule, and within budget.

The role emphasizes technical depth, business acumen, and the ability to influence stakeholders at all levels. On-site collaboration and a focus on GMP compliance are required.