Quality Applications Specialist - 157

Villalba, PR, Puerto Rico
Contracted
Medical Device
Experienced

Quality role to support product transfer activities in the engineering area. 

WHAT MAKES YOU A FIT: 

The Technical Part:

  • Bachelor's Degree in Engineering or Science with at least (2) two years of experience within the regulated industry. 
  • Bilingual (English & Spanish).
  • Good communication and writing skills.
  • Shift: 1st and according to business needs (Availability to work overtime and weekends when necessary). 
  • Certification: Lean Six Sigma 
  • Experience in: 
    • Microsoft Office, Agile, HR - ABRA Suite, Maximo, MRO Program, SAP, TEDS, Agile, Compliance Wire, Gallup On-line Tool. 
    • Evaluating, Investigating & Completion of Non- Conformance.
    • Identifying and Implementing Corrective/Preventive Actions. 

The Personality Part:    

  • Besides being able to provide guidance, you're able to work independently to solve problems and improve every aspect of the project. Add to this a commitment to serving customers with high-quality research and products, to embracing a diverse work culture, and even to the environment, and you might just be what we’re looking for!

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

  • Conducts a compliant validation process for quality information technology systems, which requires formal validation documentation. 
  • Coordinates activities with clients, programmers/developers, and operating personnel, domestic and, as appropriate, global.
  • Identifies current and anticipated requirements for compliant computerized operations and suggests methods for the identification and implementation.
  • Maintenance of the procedures, actions, and documentation necessary to ensure compliance with the appropriate federal and international regulations. 
  • Reports on the status of validation activities to fulfill regulatory requirements.
  • Performs system administration and configuration of quality information technology systems.
  • Performs investigation of non-conformance events. 
  • Initiates, recommends, and provides solutions to the Non-Conforming Product as per procedures.
  • Verifies the implementation and effectiveness of non-conforming CAPA.
  • Executes job responsibilities as established in the procedures.
  • Follows the documentation procedures Non- Conformance Resolution.
  • Investigation ( Data gathering of Quality issue).
  • Lead complaint activities with the Operating Units members. 
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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