Automation Project Manager
Job Opportunity: Automation Project Manager
Location: Dorado, PR (100% Onsite)
Positions: 1
Duration: Approximately 9 months (February–December 2025)
About the Role
ProQuality Network is seeking a dynamic and experienced Automation Project Manager to join our team on a contractual basis, working onsite with one of our esteemed clients in Dorado, PR. This opportunity involves leading critical automation and software engineering projects in a regulated medical device manufacturing environment.
Key Responsibilities:
1. Project Management
- Develop and maintain project schedules to ensure timely delivery.
- Track and manage budgets, identifying and addressing cost deviations.
- Prepare and share status reports with stakeholders and leadership.
- Allocate resources effectively and manage project priorities.
2. Change Management and Documentation
- Lead the generation and management of change notifications in compliance with regulatory processes.
- Present change proposals in regulatory forums and secure necessary approvals.
- Develop, route, and obtain formal approval for project documents.
- Complete mandatory training on change management and documentation systems.
3. Coordination of Activities
- Facilitate cross-functional meetings to align on project goals and deliverables.
- Serve as the main contact for internal teams and external vendors.
- Collaborate with validation, automation, and quality teams to ensure compliance with procedures, regulations, and standards.
4. Regulatory and Compliance
- Ensure all projects meet medical device industry standards and regulatory requirements.
- Represent project updates and changes in regulatory meetings/forums.
5. On-Site Responsibilities
- Be present at the manufacturing site to oversee project progress and resolve issues.
- Provide hands-on support for troubleshooting and system alignment.
6. Technical Knowledge
- Utilize expertise in industrial automation and software engineering lifecycles.
- Work with automation and controls teams to coordinate system integration strategies.
Required Qualifications
- Education: Bachelor’s degree in Engineering, Industrial Automation, or a related field.
- Experience:
- 3–5 years in software and industrial automation project management (medical device experience preferred).
- Familiarity with medical device regulatory requirements.
- Skills:
- Proficient in project management tools (e.g., MS Project, Smartsheet).
- Knowledge of industrial automation systems (Rockwell, Siemens, Cognex).
- Experienced in change management systems and document control.
- Strong organizational, communication, and leadership capabilities.
- Ability to handle multiple projects simultaneously.
Additional Requirements
- Onsite presence is mandatory.
- Completion of internal training on change management and documentation systems.
- Experience in regulated environments with a focus on quality and compliance.
Work Environment
The role is based entirely onsite at a manufacturing facility, requiring close collaboration with engineering, automation, production, quality, and compliance teams. Occasional travel may be required for vendor coordination or regulatory purposes.
Why Join Us?
This is a unique opportunity to play a vital role in delivering impactful automation solutions within the medical device sector. Your expertise will directly contribute to the success of key projects, ensuring compliance, quality, and efficiency.
Ready to Apply?
We invite qualified candidates to apply inside the job description withanr updated resumes and availability for a conversation. Don’t miss this chance to take the next step in your career!