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Process Validation Engineer - 134

Villalba, PR, Puerto RicoPosted 1 weeks ago
onsite

Job Description

Our #NextPiece 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, many talents.

#BeingThePiece means you're full of bright ideas and eager to innovate, always bringing top-quality results to the table.

Are you ready to #BeThePiece?

For Packaging and Sterilization services in the Manufacturing area.

WHAT MAKES YOU A FIT: 

The Technical Part:

  • Bachelor’s Degree in Engineering and two (2) years of experience within the Medical Devices Industry.
  • Bilingual: Spanish and English
  • Soft Skills: Writing and communication skills
  • Shift: 1st and according to business needs. 
  • Experience in: 
    • Ethylene oxide, steam, liquid chemical, and radiation sterilization methods
    • Process Validation, Equipment IQ, and Computer software validation knowledge
    • No sterile package design or pharma design 

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 Be The Piece?

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

  • Design manufacturing processes, procedures, and production layouts for assemblies, equipment installation, processing, machining, and material handling.
  • Design arrangement of machines within plant facilities to ensure the most efficient and productive layout.
  • Design sequence of operations and specify procedures for the fabrication of tools and equipment, and other functions that affect product performance.
  • Adapt machine or equipment design to factory and production conditions. May incorporate inspection and test requirements into the production plan.
  • Inspect performance of machinery, equipment, and tools to verify their efficiency, and investigate and initiate corrective action for problems and deficiencies to ensure product quality.
  • Develop manufacturing processes that apply to statistical process control and may develop techniques.
  • Guide engineers regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques.
  • Ensure processes and procedures comply with regulations. 

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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Process Validation Engineer - 134 at Flexible & Integrated Technical Services, LLC | Renata