The Automation Project Manager is responsible for planning, coordinating, and overseeing automation projects. Responsibilities include coordinating teams, managing budgets, and ensuring the successful implementation of automation systems to enhance operational efficiency. The Project Manager will collaborate with cross-functional teams, vendors, and clients to drive successful implementation of automation solutions in pharmaceutical, biotechnology, and medical devices environments.
Key Responsibilities:
- Manage the full life cycle of automation projects, including planning, scheduling, budgeting, and execution.
- Coordinate with engineering, compliance, IT, and operations teams to define project requirements and deliverables.
- Coordinate internal resources and third-party vendors for the flawless execution of projects.
- Develop and maintain project plans, timelines, and progress reports, ensuring milestones and deadlines are met.
- Deliver automation projects across PLC, SCADA, HMI, Batch, and DCS control systems, from design to validation.
- Oversee design, installation, validation, and commissioning of automation systems and equipment.
- Ensure compliance with industry regulations, standards, and company policies (FDA, GMP, ISO, etc., as applicable).
- Facilitate communication between stakeholders, contractors, and vendors to ensure alignment and resolve issues.
- Identify risks, develop mitigation strategies, and monitor project progress to address challenges proactively.
- Manage resources effectively, including internal staff and third-party contractors.
- Support continuous improvement by identifying opportunities to enhance automation processes and project management practices.
- Conduct post-project evaluations to ensure lessons learned are captured and applied.
Education
- Bachelor's degree in Engineering (Electrical, Control Systems), Computer Science, or a related field.
- PMP certification (preferred, not required).
Experience
- 3--6 years of experience managing automation, controls, or engineering projects within pharmaceutical, biotechnology, or medical device industries.
Skills
- Strong knowledge of automation technologies: PLC, HMI, SCADA, Batch, and DCS systems.
- Experience with Computer System Validation (CSV), cGMP environments, and regulated manufacturing.
- Proficiency in project management tools (MS Project, Asana, Jira, or similar).
- Familiarity with Lean Six Sigma or continuous improvement methodologies preferred.
- Strong analytical, organizational, and leadership skills.
- Excellent communication skills (written and verbal) with the ability to work cross-functionally.
Other requirements
- Work Schedule: Require flexible time, including the capacity to work overtime, different schedules, and holidays or weekends as needed, to meet shutdown demands.
- Travel Requirements: Availability to work and travel within the United States.
Synerlution Inc. is committed to providing equal employment opportunities for all employees and applicants, regardless of race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, or veteran status. We feel that having a diverse staff increases our capacity to drive synergy through solutions for our clients. We are committed to fostering an inclusive environment in which all employees feel comfortable sharing their unique ideas and talents.
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