Commissioning & Qualification Lead (C&Q)

    Highlights

    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. AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job) Validation, Commissioning Qualification, Technical Writing, Protocol Drafting.

    Numbers & Facts

    LocationJuncos
    Websitehttp://www.fitspr.com

    Description

    For C&Q services in Capital Projects area.

    WHAT MAKES YOU A FIT: 
    The Technical Part:
    • Bachelor's Degree in Science or Engineering with five (5) years of experience in the validation life cycle, within the pharmaceutical industry.
    • Bilingual (English & Spanish).
    • Shift: Administrative, and according to business needs. 
    • Experience in: 
      • Generation & Execution Protocols Commissioning, Qualification, and validation.
      • Develop validation engineering policies and procedures.
      • Project Management 

    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 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)
    • Validation, Commissioning Qualification, Technical Writing, Protocol Drafting.
    • Review and Execution of deviation processes. 
    • Develop validation engineering policies and procedures that affect multiple organizational units.
    • Supervise, coordinate, and review the work of a small staff of engineers and/or technicians on an ongoing basis and on a project basis.
    • Employ advanced validation engineering techniques and/or modifications of advanced techniques within the area of validation engineering expertise.
    • Apply knowledge of validation engineering principles and practices outside of the area of expertise to a broad variety of assignments in related fields.
    • Develop technical solutions to complex problems that require regular ingenuity and creativity.
    • Work with manufacturing, process development, utilities, facilities, labs, and/or quality assurance in developing requirements and recommendations for large and/or highly complex process, system/facility modifications.


    WHO WE ARE:

    We are a Service Provider company different from the rest. We pride ourselves in 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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