Sr. Software Quality Engineer

Reposted 3 Days Ago
Be an Early Applicant
Juncos
In-Office
Senior level
Pharmaceutical
The Role
The role involves developing software quality standards, evaluating software activities, ensuring compliance with project requirements, and directing software verification and validation.
Summary Generated by Built In

For Automation and Troubleshooting services in the Engineering and Manufacturing area. 

WHAT MAKES YOU A FIT: 

The Technical Part:

  • Bachelor's Degree in Engineering with at least (5) years of experience in programming/troubleshooting within the regulated industry. 
  • Bilingual (English & Spanish).
  • Good communication skills.
  • Shift: 1st, 2nd shift, and weekends if needed due to production schedule. 
  • Experience in: 
    • Automation / Controls / Programming 
    • Computer Systems Validations
    • CAPA / Investigations / Root Cause Analysis 

The Personality Part:    

  • Besides being an Automation Pro, you’re able to analyze data so that not a single inconsistency gets past you (which allows you to be an amazing problem-solver). You’re also a skilled multitasker with an incredible ability to set priorities. 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)

  • Develops, modifies, applies, and maintains standards for software systems quality, operating methods, processes, and procedures.
  • Evaluates software systems activities, including requirements, design, development, documentation, integration, testing, verification, and validation. Defines appropriate measures to ensure product quality.
  • Develops overall operating criteria to ensure implementation of the software quality program according to project, process, and contract requirements and objectives.
  • Ensures that projects and process control documentation are compliant with requirements, objectives, and/or contracts.
  • Reviews software systems design, change specifications, and plans against contractual and/or process requirements.
  • Reviews include applicable specifications, materials, tools, techniques, and methodologies.
  • Provides or directs verification and validation of software system requirements, traceability, and testability.
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

Automation
Computer Systems Validations
Controls
Programming
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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