QA Engineer

Posted 19 Days Ago
Be an Early Applicant
San Lorenzo
In-Office
Mid level
Pharmaceutical
The Role
The QA Engineer will manage validation life cycle activities, review documentation, ensure compliance with regulations, and investigate product failures.
Summary Generated by Built In

For Validation services in the Quality area.

WHAT MAKES YOU A FIT: 

The Technical Part:

  • Bachelor’s degree in Engineering and previous exposure in Validation Life Cycle activities within the Pharmaceutical or Medical Device industry. 
  • Shift: Administrative & according to business needs
  • Bilingual: (Spanish and English)  
  • Experience in:
    • Quality: reviewing validation documentation, procedures and change control.
    • Sampling plans.

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)

  • Knowledge of validation methodologies (IQ, OQ, PQ) and protocols.
  • Familiarity with Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and FDA/ISO regulatory requirements.
  • Proficient in using data analysis tools (Excel, Minitab, or equivalent).
  • Strong analytical and problem-solving skills. Excellent technical writing and documentation skills.
  • Willingness to work in cleanroom or controlled environments.
  • Knowledge of safety procedures and compliance with EHS regulations.
  • Ensure timely, thorough and complete execution of all protocols, meeting FDA requirements.
  • Ensure that all new and existing protocols are effectively integrated into manufacturing processes. 
  • Ensure documentation is thorough, accurate and entered on a timely basis into the quality system.
  • Ensures complete and thorough investigation of all product failures, batch failures and deviations associated with validation sampling and testing.
  • Develops documentation of investigations and communicates findings to ensure chance of recurrence is significantly minimized and resolution satisfies validation requirements.

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?

Top Skills

Excel
Minitab
Am I A Good Fit?
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The Company
HQ: Guaynabo, PR
76 Employees
Year Founded: 2008

What We Do

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 We The Right Piece For You?
We are:

Experienced and knowledgeable in the Industry
Committed to Safety
Always compliant with FDA Regulations & Audits
Cost Effective
Proven successful track record
Over ten (10) years of experience

If you'd like to apply to any of our open positions, send us your updated resume in Word or PDF Format to [email protected]

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