JT573 - QUALITY ENGINEER I

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities: 

• Develops, modifies, applies, and maintains standards for software systems quality operating methods, processes, and procedures.
• Conducts evaluation of software systems activities including requirements, design, development, documentation, integration, test, verification, and validation.
• Provides verification and validation of software system requirements, traceability, and testability. 
• Work with peers to address process changes to existing work instructions and/or standard operating procedures.

Qualifications:

• Bachelor's degree in engineering
• 1 to 3 years of relevant experience 
• Process and Computerized Systems Validation
• Experience in FDA regulated industries
• Excellent verbal and written communication skills (English and Spanish).
• Availability for 1st shift