Process Engineer I - 019

Posted Yesterday
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Ponce
Junior
Pharmaceutical
The Role
As a Process Engineer I, you will recommend and implement process modifications to enhance production efficiency, conduct validations, collaborate with design teams, and ensure compliance with regulations within the Pharmaceutical and Medical Devices industry.
Summary Generated by Built In

For Validation services in the Engineering area.

WHAT MAKES YOU A FIT: 

The Technical Part:

  • Bachelor’s Degree in Engineering and two (2) years of exposure within the Pharmaceutical & Medical Devices Industry.
  • Bilingual: Spanish and English
  • Soft Skills: Organization and Communication Skills. 
  • Shift: 1st Shift. 
  • Experience in: 
    • Root Cause Analysis
    • Validation Lifecycle
    • 1st Level Troubleshooting 
    • Equipment Validation
    • New Product and Capacity increase. 

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)

  • Recommends and implements equipment and process modifications to meet quality standards and improve production efficiencies, and manufacturing.
  • Integrates equipment and material capabilities to meet process module and technology target specifications.
  • Review product development requirements for compatibility with processing methods to determine costs and schedules.
  • Interacts with product design and development personnel to ensure that processes and designs are compatible.
  • May develop and conduct statistical analysis or recommend additions to document work.
  • Leads the innovation, development, and optimization of new manufacturing concepts, processes, and procedures for transfer to manufacturing operations.
  • Develop, execute, and close protocols required for the validation lifecycle.
  • Supports equipment installation and assessment of inputs, outputs, and alignment to requirements.
  • Ensures processes and procedures comply with regulations.
  • Develops manufacturing processes that are applicable to statistical process control and may develop those techniques including the measurement.

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?

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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