Project Manager (Lifesciences Industry)

Posted Yesterday
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New Albany, OH, USA
In-Office
Senior level
Information Technology
The Role
Leads capital projects in regulated Life Sciences manufacturing and quality environments. Responsibilities include planning, scheduling, budgeting, risk management, vendor coordination, stakeholder communication, and cross-functional team leadership. Ensures compliance with GMP, FDA, GxP, validation, and internal quality requirements while managing technical platforms and project delivery across IT, automation, quality, engineering, and validation teams. This is a full-time onsite role in Ohio.
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 a related field
  • At least 5 years of project management experience in the Medical Devices and Life Sciences industries
  • Experience managing capital projects
  • Knowledge of MES, LIMS, ERP, SCADA, Historians, or other digital platforms
  • Strong understanding of regulated environments and validation requirements
  • Proficiency in project management tools and methodologies
  • Excellent leadership, organizational, and communication skills
  • PMP certification
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The Company
HQ: San Juan, PR
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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