Quality Engineer - CSV

Posted 5 Days Ago
Be an Early Applicant
Añasco
Mid level
Pharmaceutical
The Role
The Quality Engineer will implement quality engineering processes, support validation and certification of products and methods, generate test protocols, and collaborate with cross-functional teams to deliver projects while maintaining quality standards.
Summary Generated by Built In

 For Quality services in the Engineering & Manufacturing areas. 

WHAT MAKES YOU A FIT: 

The Technical Part:

  • Bachelor's Degree in Engineering and at least four (4) years of previous exposure in CSV and Periodic Review activities within the Pharmaceutical or Medical Devices industry. 
  • Bilingual, Spanish and English (good communications)
  • Shift: Administrative & according to business needs 
  • Experience in:
    • Validation Life Cycle (CSV
    • Change control 
    • Periodic Reviews
    • GMP & GDP 

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)

  • Support the implementation of effective quality engineering processes for new products, processes, and technology.
  • Provides support to the validation and certification of processes, test methods, equipment, software, utilities, and facilities as required.
  • Generates test protocols, monitors testing, issues qualification test reports, and approves qualifications plans/reports.
  • Provides support on activities, documents, and records requiring Quality Engineering review and/or approval as deemed necessary.
  • Alerts the organization to issues in time to resolve potential adverse effects on the customer, company image, or reputation of the business.
  • Works with multi-functional teams to establish project plans and ensures uninterrupted support to new projects balanced with manufacturing operations.
  • Develops standard operating procedures, and specifications, and provides technical transfer and validation support.
  • Utilizes appropriate risk management tools to prevent unanticipated failure modes and improve the capability of processes. 

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

Csv
The Company
HQ: Guaynabo, PR
76 Employees
On-site Workplace
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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