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Manufacturing Engineer

EQVAL

Villalba, Villalba

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JOB DETAILS
JOB TYPE
Full-time
SKILLS
Analysis Skills, Biotech and Pharmaceutical, Communication Skills, Computer Software, Corrective Action, Cross-Functional, English Language, Equipment Validation, Health Insurance, Maintain Compliance, Manufacturing, Manufacturing Engineering, Manufacturing Operations, Manufacturing/Industrial Processes, Medical Equipment, Pharmacy, Problem Solving Skills, Process Improvement, Process Validation, Production Support, Regulatory Requirements, Root Cause Analysis, Software Validation, Spanish Language, Support Documentation, System Validation, Team Player, Technical Support, Technical Writing, Time Management, Validation Documentation, Writing Skills
LOCATION
Villalba, Villalba
POSTED
29 days ago

EQVAL Group, Inc. is a company that provides services to the manufacturing industry (Medical Devices, Pharmaceuticals, Biotechnologies, others). We work with an extraordinary group of professionals (employees and contractors) to accomplish the requirements established by our customers, in order to perform and provide a highly effective service.

We are seeking a Manufacturing Engineer to provide technical and sustaining engineering support in a manufacturing environment. This role focuses on process validation, equipment qualification (IQ), and computer software validation, while supporting production efficiency and product quality. The ideal candidate will have strong problem-solving skills, including root cause analysis, and the ability to work cross-functionally to meet project timelines. This is an on-site role in Villalba, Puerto Rico.

Key Requirements:

  • Bachelor’s Degree in Engineering
  • Minimum of 2+ years of relevant experience
  • Experience in Process Validation, Equipment IQ, and Computer Software Validation
  • Knowledge of statistical techniques
  • Strong investigation and root cause analysis skills
  • Experience supporting manufacturing environments
  • Strong technical writing and communication skills (English & Spanish)
  • Ability to manage priorities and meet project deadlines

Key Responsibilities:

  • Provide technical and sustaining engineering support for manufacturing operations
  • Support and execute process validation and equipment qualification (IQ) activities
  • Participate in computer software validation (CSV) efforts
  • Investigate equipment and process issues, perform root cause analysis, and implement corrective actions
  • Monitor and evaluate machinery and equipment performance to ensure efficiency and product quality
  • Develop and improve manufacturing processes using statistical techniques
  • Collaborate with cross-functional teams to meet project objectives and timelines
  • Ensure compliance with internal procedures and regulatory requirements
  • Support documentation efforts, including technical reports and validation-related documentation

Benefits:

  • Health insurance (Medical, Dental, Vision, Pharmacy)
  • Life Insurance
  • Paid time off (PTO)
  • Holidays
  • Professional Growth (Courses and Certifications by EQVAL Academy)
  • Referral program
  • Productivity incentive
Please note that this is an on-site position in Villalba, PR (M–F).

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About the Company

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EQVAL