Sr. Process Automation Specialist

    Highlights

    Move through project phases — planning and design, procurement, execution/construction, commissioning and qualification (FAT/SAT, CSV, PQ), and close-out. 5+ years in pharmaceutical operations/manufacturing with project management experience, including 4+ years in process automation and 2+ years in CSV.

    Numbers & Facts

    LocationManati
    Websitehttp://www.fitspr.com

    Description

    For Automation services in the Capital Project area.

    WHAT MAKES YOU A FIT: 

    The Technical Part:

    • Bachelor's degree in Engineering, Computer Science, Information Systems, or related field. 5+ years in pharmaceutical operations/manufacturing with project management experience, including 4+ years in process automation and 2+ years in CSV.
    • Strong knowledge of cGMP, FDA/EMA regulations, and 21 CFR Part 1
    • Bilingual: Spanish and English (verbal/ written)
    • Shift: Administrative and according to business needs. 
    • Experience in:
      • CMMS systems (e.g., Maximo).
      • High level of expertise in Rockwell Automation platforms.
      • Siemens, Wonderware, and FactoryTalk Batch.
      • Virtualization platforms (VMware vSphere).
      • MES systems (e.g., Syncade).
      • OSIsoft / AVEVA PI systems and Microsoft SQL databases.
    The Personality Part:    
    • Our Next Piece is someone who treats everyone they meet like family, especially our resources, clients, and team members. In other words, being a customer service pro is one of your (many) talents. Being the Piece means you're full of bright ideas and eager to innovate, always bringing top-quality results to the table. Are you ready to take on this new challenge?

    AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job)

    • Check in with vendors, contractors, and system integrators on active automation/IT projects (PLCs, HMI, SCADA, DCS/BAS installations, upgrades, commissioning).
    • Troubleshoot technical issues that come up during installation, start-up, or qualification activities.
    • Monitor project schedules and flag risks or delays to stakeholders.
    • Coordinate with EHS, Quality, and Manufacturing on day-to-day project matters.
    • Prepare and present weekly project status reports (milestones, budget, risks).
    • Attend cross-functional meetings with Engineering, Quality, Validation, IT, and Manufacturing.
    • Review vendor quotes and update technical documentation (URS, FRS, DS) as designs evolve.
    • Move through project phases — planning and design, procurement, execution/construction, commissioning and qualification (FAT/SAT, CSV, PQ), and close-out.
    • Support audits, deviations, and CAPAs as needed.
    • Occasionally work irregular hours during critical milestones (start-up, cutover, audits)

    WHO WE ARE:

    We are a Service Provider company, different from the rest. We pride ourselves on how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities, and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented, and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device, and Manufacturing industry clients with top-notch quality talent. We're FITS! 

    Are you the Next Piece?

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