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President at Smart Precise Solutions, Inc.
Summary:
We are seeking a Automation Project Manager to lead the execution of projects in the field of industrial automation and software engineering. This position will play a key role in planning, managing, and monitoring projects, ensuring that timelines and budgets are met. The ideal candidate will have experience managing projects in the medical device manufacturing environment, with a focus on adherence to regulatory requirements and standards.
Key Responsibilities:
Develop, manage, and maintain project schedules, ensuring timely completion of deliverables.Track budgets and expenses, ensuring adherence to financial constraints and flagging any deviations.Generate regular project status reports for stakeholders and leadership.Ensure proper resource allocation and manage project priorities to ensure alignment with overall business goals.Lead and generate change notifications, ensuring full compliance with documentation systems and processes.Present change proposals in regulatory forums, ensuring necessary approvals are obtained.Develop and route project-related documents through the change management system for formal approval.Participate in required trainings on change management and documentation systems.Facilitate cross-functional team meetings to ensure alignment on project goals, timelines, and deliverables.Serve as the main point of contact for internal teams and external vendors, ensuring smooth execution of project activities.Coordinate with validation, automation, and quality teams to ensure project deliverables comply with BSC procedures, medical device regulations, and industry standards.Ensure all projects adhere to medical device industry standards and regulatory requirements.Attend regulatory meetings and forums to represent project changes and provide timely updates as required.Qualifications:
·Education: Bachelor's degree in engineering, Industrial Automation, or a related field.
·Experience: 3-5 years of experience managing software and industrial automation projects, preferably in a medical device manufacturing environment.
·Knowledge: Familiarity with medical device regulatory requirements and industry standards.
Skills and Competencies:
· Proficiency in project management tools such as MS Project or Smartsheet.
· Familiarity with industrial automation systems (e.g., Rockwell, Siemens, Cognex, etc.).
· Experience with change management systems and document control processes.
· Strong organizational, communication, and leadership skills.
· Ability to manage multiple projects and priorities simultaneously.
Additional Requirements:
On-site presence is required.Ability to attend and complete internal trainings on change management and documentation systems.Experience working in regulated environments with a focus on quality and compliance.The role is based on-site at a manufacturing plant and requires close coordination with engineering, automation, production, quality, and compliance teams.Occasional travel may be required for vendor coordination or participation in regulatory meetings.Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Project Management and Information Technology
Industries
Business Consulting and Services
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