As a Project Manager, you’ll lead transformative automation projects, setting technical vision and strategy to drive efficiency, regulatory compliance, and operational excellence. This role provides a unique opportunity to collaborate with industry leaders in pharmaceutical manufacturing, shaping advanced automation solutions within the pharmaceutical sector. At PACIV, you’ll be part of a collaborative environment that supports continuous learning, career growth, and the freedom to innovate in an industry redefining the future of manufacturing and compliance standards.
If you’re ready to take on a leadership role in automation project management and drive meaningful changes, the Automation Project Manager position at PACIV is where your expertise meets the opportunity. Join us and make your mark on an industry-leading team dedicated to innovation and excellence!
About PACIV: We are a global leader in control systems integration and regulatory compliance engineering. For over two decades, we’ve been at the forefront of innovation and operational excellence for clients in Biopharma, Life Sciences, Medical Devices, Food & Beverage, and Water/Wastewater industries. For more information, check out our website at www.paciv.com.
Position Location: Jayuya, Puerto Rico
Key Responsibilities:
- Project Leadership: Provide clear direction and accountability, ensuring the project aligns with the approved scope, schedule, and cost plans.
- Compliance & Quality: Ensure compliance with project planning documents and PMO-defined procedures and guidelines.
- Progress Monitoring: Plan, monitor, and control project activities within the designated area, and communicate progress and staffing needs to Program Automation Leaders and Managers.
- Cross-functional Collaboration: Work closely with MES, BMS, and Data Historian project managers to coordinate the delivery of each system, ensuring smooth integration.
- Stakeholder Communication: Interface with Global Facilities Delivery (GFD) PM, other disciplines, and stakeholders to align project outcomes with business needs.
- Resource Management: Lead and manage automation resources, ensuring the team is equipped to achieve successful project execution.
- Proposal & System Integration: Lead preparation of requests for proposals, conducted bid analysis and initiated system integration efforts within the area.
- Reporting & Documentation: Provide progress updates to the PMO, contribute to monthly reports, document lessons learned, and support cost estimation for project gate reviews.
- Risk Management: Participate in risk identification and response planning and manage project automation integrated change control.
- Training & Compliance: Support and organize training modules, ensuring team members meet all required training compliance standards.
Required Qualifications:
- Education: Bachelor’s degree in engineering or equivalent experience.
- Experience: 5+ years in Automation Project Management within the pharmaceutical industry, with experience in large-scale automation projects.
- Technical Expertise: Experience with DeltaV controlled/batch-based capital projects is preferred, along with proficiency in project management tools such as P6/MS Project, metrics, and risk management.
- Industry Knowledge: Familiarity with GMPs, regulatory requirements, and computer system validation is highly desirable.
- Project Management Credencial
PACIV provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status,
sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
Top Skills
What We Do
PACIV, Inc. (Process Automation – Controls.Instruments.Validations) was founded and registered as a corporation in the Commonwealth of Puerto Rico in 1997. Listening to our clients' desire for local support and standardization among their facilities, we opened our Indiana office (PACIV-USA, LLC) in 2003. Moreover, in 2011 we opened PACIV-Ireland in Cork, Ireland.
Our expansion, including international presence with local resources, responds to the needs of our Life Sciences multinational clients regarding replication and consistency of implementation, who demand our life sciences automation and regulatory compliance solutions in a localized market format. Our thorough understanding of the challenges faced by the Life Science sector and our collaborative approach with our clients has enabled us to become a leading Life Sciences automation and regulatory compliance service company. Since our inception, we provide our Life Sciences clients with our services in their multiple manufacturing sites worldwide.
The fact that we hold Master Service Agreements (MSA’s) and Preferred Vendor status with the world’s leading Life Science Companies serves a testimony of our quality of service and leadership standing within the Life Science industry. We attract and develop the best talent which allows us to provide our demanding clients with the right knowledge and expertise ensuring we provide significant value within our automation solutions and services.
