Project Manager (Lifesciences Industry)

Inteldot

$90K — $120K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in engineering, Computer Science, Life Sciences, or related field.
  • Minimum 5 years of project management experience in Medical Devices and Life Sciences.
  • Proven experience managing capital projects, specifically in Packaging projects.
  • Knowledge of digital platforms like MES, LIMS, ERP, SCADA, Historians.
  • Strong understanding of regulated environments and validation requirements.
  • Proficient in project management tools and methodologies; PMP certification is a plus.
  • Excellent leadership, organizational, and communication skills.

Responsibilities

  • Lead planning, execution, and delivery of capital projects in Life Sciences.
  • Develop detailed project plans, timelines, and risk mitigation strategies.
  • Collaborate with cross-functional teams, including IT, quality, and engineering.
  • Ensure compliance with industry regulations and internal quality systems.
  • Manage vendors and third-party providers to meet project goals.
  • Monitor project performance, manage scope, budget, and schedule.
  • Facilitate effective communication between business and technical teams.

Benefits

  • Full-time, onsite position in Ohio.
  • Collaborative and dynamic work environment.
  • Opportunity to work within a highly regulated industry.
Full Job Description
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.

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