Project Manager (Lifesciences Industry)

Posted Yesterday
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New Albany, OH, USA
In-Office
Senior level
Information Technology
The Role
Lead planning, execution, and delivery of capital projects in Life Sciences manufacturing. Develop project plans, manage scope, budget, schedule, vendors and cross-functional teams. Ensure GMP/FDA/GxP compliance and validation, coordinate IT/automation/quality/engineering stakeholders, and provide status updates to leadership.
Summary Generated by Built In

We are seeking a highly motivated and experienced Project Manager to lead and deliver capital projects in the Life Sciences industry. This role requires a hands-on professional with a strong track record of managing cross-functional teams and delivering technical projects in compliance-driven environments. The selected candidate will work onsite in Ohio, partnering with client teams and vendors to ensure successful project execution.

Key Responsibilities:

  • Lead the planning, execution, and delivery of capital projects within Life Sciences manufacturing or quality environments.

  • Develop detailed project plans, timelines, resource allocation, and risk mitigation strategies.

  • Collaborate with cross-functional stakeholders including IT, automation, quality, validation, and engineering teams.

  • Ensure compliance with industry regulations (GMP, FDA, GxP) and internal quality systems throughout project execution.

  • Manage vendors and third-party service providers to align with project goals.

  • Monitor project performance, manage scope, budget, and schedule, and provide regular status updates to leadership.

  • Facilitate effective communication and coordination between business and technical teams.

Required Qualifications:

  • Bachelor’s degree in engineering, Computer Science, Life Sciences, or related field.

  • Minimum 5 years of project management experience in the Medical Devices and Life Sciences industries.

  • Proven experience managing capital projects (Packaging projects preferred).

  • Knowledge with MES, LIMS, ERP, SCADA, Historians, or other digital platforms.

  • Strong understanding of regulated environments and validation requirements.

  • Proficient in project management tools and methodologies (PMP certification a plus).

  • Excellent leadership, organizational, and communication skills.

Work Environment:

  • Full-time, onsite position in Ohio.

  • Collaborative and dynamic environment within a highly regulated industry.

Skills Required

  • Bachelor's degree in Engineering, Computer Science, Life Sciences, or related field
  • Minimum 5 years project management experience in Medical Devices and Life Sciences industries
  • Proven experience managing capital projects
  • Experience with Packaging projects
  • Knowledge of MES, LIMS, ERP, SCADA, Historians or other digital platforms
  • Strong understanding of regulated environments and validation requirements (GMP, FDA, GxP)
  • Proficient in project management tools and methodologies
  • PMP certification
  • Excellent leadership, organizational, and communication skills
  • Ability to work full-time onsite in Ohio
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The Company
HQ: San Juan
19 Employees
Year Founded: 2004

What We Do

Inteldot offers custom turn-key systems, systems integration, MES eBR configuration and integration solutions, business intelligence and analytics and technical staffing. We have been providing the Pharmaceutical, Manufacturing and Medical Device industries with services for a variety of applications since 2004

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