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:

• Engineer or Specialist in charge for equipment and process validation including IQ, OQ, TMV/MSA, PQ protocol generation and execution.
• Resource will be hands-on with automation, tooling, and maintenance technicians to coordinate and follow-up on equipment troubleshooting.
• Repairs or service required to assure that equipment validation is successful and for resolution of any deviation.
• Good team-member, with communication and time management skills to keep-up with project timeline

Qualifications:

•  Bachelor Degree in Engineering Preferred or Science
• Two (2) years of experience in Validations including IQ, OQ, TMV/MSA, PQ protocol generation and execution.
• Experience in equipment validations protocol generation, execution and report
• Good time management skills to comply with timeline