• FITS LLC (Manati, PR)
    …the science and physics involved in designing, installing, commissioning, and validation /qualification of computerized systems and PLCs as applied to ... pharmaceutical production environments. Broad knowledge of relevant governmental regulations,...regulatory audits (FDA, EMA, Otsuka, Sanofi, etc. Knowledge of pharmaceutical business processes and equipment. Knowledge of mechanical concepts,… more
    Upward (07/11/25)
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  • Quality Consulting Group (Villalba, PR)
    QUALITY CONSULTING GROUP, a leader in the pharmaceutical , biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and ... Change control of Medical Devices Equipment Commissioning / Qualification Process Validation Computer System Validation (CSV) Manufacturing, Packaging and… more
    Upward (07/15/25)
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  • Validation Engineer

    Mentor Technical Group (Ponce, PR)
    …Mexico, Germany, Canada, and South America. Qualifications Requirements/Knowledge/Education/Skills: + Engineer or Specialist for equipment and process validation ... MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices… more
    Mentor Technical Group (07/06/25)
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  • Validation Specialist - Serialization

    Mentor Technical Group (Juncos, PR)
    …Canada, and South America. Job Summary: We are seeking a meticulous and experienced Validation Engineer specializing in Serialization to join our team. The ideal ... MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices… more
    Mentor Technical Group (05/17/25)
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  • Staff Automation Engineer , OT…

    J&J Family of Companies (Anasco, PR)
    …**We are searching for the best talent for Staff Automation Engineer , OT and Cybersecurity.** **Purpose:** We are seeking an experienced automation ... + Lead small to medium-sized multidisciplinary teams including Computer System Validation (CSV) specialists, IT professionals, and various engineering fields + Apply… more
    J&J Family of Companies (07/23/25)
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  • Staff Automation Engineer , Systems

    J&J Family of Companies (Anasco, PR)
    …**We are searching for the best talent for Staff Automation Engineer , Systems.** **Purpose:** We are seeking an experienced automation professional to ... + Lead small to medium-sized multidisciplinary teams including Computer System Validation (CSV) specialists, IT professionals, and various engineering fields + Apply… more
    J&J Family of Companies (07/22/25)
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  • Engineer

    Mentor Technical Group (Juncos, PR)
    …experience + Drug substance manufacturing/technical support + Working knowledge of pharmaceutical /biotech processes + Familiarity with validation processes + ... MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices… more
    Mentor Technical Group (06/18/25)
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  • Engineer

    Mentor Technical Group (Juncos, PR)
    …MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices ... manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation departments in developing requirements and recommendations for system… more
    Mentor Technical Group (06/18/25)
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  • Jt592 - Process Engineer II

    Quality Consulting Group (Villalba, PR)
    QUALITY CONSULTING GROUP, a leader in the pharmaceutical , biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and ... & USA. Responsibilities: + Responsible for developing, executing, and managing validation activities for utilities systems in compliance with regulatory requirements… more
    Quality Consulting Group (07/09/25)
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  • Process Engineer

    Mentor Technical Group (Ponce, PR)
    …a Process Engineer with strong experience in validations, including Master Validation Plans, IQ, OQ, MSA, PQ, and related activities. + The candidate must ... has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines....and have at least two years of experience in validation within a medical device company. + Validation more
    Mentor Technical Group (05/17/25)
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