Project Manager - Capital Projects

Posted 5 Days Ago
Be an Early Applicant
Boulder, CO, USA
In-Office
114K-157K Annually
Senior level
Biotech
The Role
Lead site CAPEX projects from requirements through deployment, managing scope, schedule, budget, risk mitigation, cashflow forecasting, and governance. Coordinate cross-functional teams and vendors, report outcomes and risks, ensure cGMP/GxP compliance, and provide technical decision-making. Manage and develop staff, oversee onboarding/training, and maintain stakeholder communications using MS Project, MS Planner, and Power BI.
Summary Generated by Built In

The Project Manager, CAPEX is responsible for leading projects from requirements definition through deployment, identifying schedules, scopes, budget estimations, and implementation plans, including risk mitigation. They will perform the following objectives:

  • Coordinate internal and external resources to ensure that projects adhere to scope, schedule, and budget.
  • Analyze project status and, when necessary, revise the scope, schedule, or budget to ensure that project requirements can be met.
  • Manage the CAPEX program for the site; to include cashflow forecasting, prioritization, commitments, tracking variances to budget, and facilitation of project governance.
  • Establish and maintain relationships with relevant client stakeholders, providing day-to-day contact on project status and changes.
  • Establish and maintain processes for managing scope during the project lifecycle, setting quality and performance standards, and assessing risks.
  • Structure and manage integrated, multitrack performance databases for digital, print, social, broadcast, and experiential projects.
  • Develop and maintain partnerships with third-party resources, including vendors and researchers.
  • Assign and monitor resources to ensure project efficiency and maximize deliverables.
  • Report project outcomes and/or risks to the appropriate management channels and escalate issues, as necessary, according to project work plan.
  • Ensure alignment and coordinates with other functions such as Engineering, Validation, Maintenance, Manufacturing, MS&T, AFS, Process Development, and Quality Assurance. Supports efforts of the organization across functional boundaries.
  • Provide technical decision-making regarding project implementation strategies as well as requirements for projects and change controls.
  • Provide exceptional customer service to internal and external clients.
  • Employee must have the ability to interface effectively with personnel across engineering, validation, maintenance, and other technical disciplines. Strong attention to deadlines and budgetary guidelines
  • Proven success working with all levels of management.
  • Strong written and verbal communication skills
  • Excellent presentation skills

Employee will actively manage a team of full-time employees and contractors. This includes the following:

  • Ensuring adequate onboarding, support administration, and training for staff
  • Providing managerial support for staff working in cross functional teams
  • Providing technical guidance to ensure work is completed in a compliant and efficient manner.
  • Ensuring adequate resource management to ensure projects are adequately staffed with trained team members and that staff can maintain work life balance.
  • Facilitating staff development

Minimum Requirements:

  • Minimum of Bachelor’s degree in an engineering, or biochemical engineering discipline and 8+ experience in the pharmaceutical/biotechnology field equivalent required and 5+ years management experience. Experience to include minimum of 5 years project management, 5 years GxP operations.
  • Established knowledge of biopharmaceutical manufacturing, good engineering practices, and equipment design and qualification. Strong technical writing and communication skills.
  • Proficiency with MS Project
  • Familiarity with MS Planner and Power BI
  • Ability to use negotiation skills drive to resolution on critical issues. Ability to summarize issues and present to executive management.
  • A broad understanding of applicable codes and regulations. Knowledge of Quality Systems and cGMP requirements for multiple regulatory jurisdictions (FDA, EU, ICH) and the ability to effectively evaluate and escalate risk is required.
  • Demonstrated track record in the following key areas:
  • Strong problem-solving capacity
  • Results orientation
  • Strong communication and presentation skills
  • Strong orientation for quality and customer service
  • High level of integrity and personal responsibility
  • Communication skills within all levels of an organization
  • Risk assessment and risk management
  • Project management including project delivery under aggressive timelines
  • Staff development and coaching
  • Additional Preferred Qualifications:
  • Background in Validation and Automation scope
  • PMP certification
  • LEAN / Six Sigma certification

Salary Range:

$114,000 - $156,750

Salary provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidate’s qualifications and experience and may be different from the provided value. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid FTO and holidays, 401K matching with 100% vesting upon hire and employee recognition programs.  

KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.

I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.

I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

Skills Required

  • Bachelor's degree in engineering or biochemical engineering
  • 8+ years experience in pharmaceutical/biotechnology field
  • 5+ years management experience
  • Minimum 5 years project management experience
  • Minimum 5 years GxP operations experience
  • Established knowledge of biopharmaceutical manufacturing, good engineering practices, and equipment design and qualification
  • Knowledge of Quality Systems and cGMP requirements for multiple regulatory jurisdictions (FDA, EU, ICH) and risk assessment capability
  • Proficiency with MS Project
  • Familiarity with MS Planner and Power BI
  • Strong technical writing, communication, presentation, and negotiation skills; ability to present to executive management
  • Demonstrated problem-solving, results orientation, customer service focus, integrity, and ability to deliver projects under aggressive timelines
  • Experience managing teams including onboarding, training, resource management, and staff development
  • Ability to interface with engineering, validation, maintenance, manufacturing, MS&T, AFS, process development, and QA
  • Ability to structure and manage integrated performance databases and manage vendor/third-party relationships
  • Background in Validation and Automation scope
  • PMP certification
  • LEAN / Six Sigma certification

KBI Biopharma Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about KBI Biopharma and has not been reviewed or approved by KBI Biopharma.

  • Healthcare Strength Health coverage includes medical, dental, and vision with HSA/FSA options, alongside life and disability insurance. Employer-verified listings indicate solid foundational coverage across sites.
  • Leave & Time Off Breadth PTO and paid holidays are provided, with flexible or “unlimited” PTO available in some salaried roles and standard accrual with limited rollover elsewhere. This breadth supports time away options across job families.
  • Parental & Family Support Parental leave is available, with indications of 12 weeks for U.S. employees in recent materials. Maternity and paternity leave are included as part of the package.

KBI Biopharma Insights

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The Company
Boulder , CO
1,282 Employees
Year Founded: 1996

What We Do

KBI Biopharma is an award-winning biopharmaceutical contract services organization providing fully-integrated, accelerated drug development and biomanufacturing services to pharmaceutical and biotechnology companies globally. With each of our 500+ client partners, we have worked closely to personalize and rapidly accelerate their drug development programs. Built upon a foundation of world-class analytical capabilities, we deliver efficient process development and clinical and commercial cGMP manufacturing services for mammalian, microbial, and cell therapy programs. KBI is proud to be a JSR Life Sciences Company.

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