CQV Lead: Validation & Commissioning Expert

FITS, LLC; Gurabo (PR); On-site; USD 60,000 - 80,000; Full time

Job summary

FITS, LLC in Gurabo, Puerto Rico is seeking qualified candidates for Validation and Commissioning & Qualification support. The role requires a Bachelor’s Degree in Life Science or Engineering and expertise in the Validation Life Cycle within the Pharmaceutical Industry.

The candidate should be bilingual in Spanish and English and possess good documentation skills, along with experience in Process Commissioning and Validation coordination. Day-to-day responsibilities include project planning, coordination meetings, and management of CQV documentation.

Qualifications

• Previous years of exposure in Validation Life Cycle within the Pharmaceutical Industry.
• Experience in Process Commissioning and Qualification.
• Experience in Validation coordination activities.

Responsibilities

• Development of an overall CQ plan with the Client project scheduler.
• Lead weekly multidisciplinary CQV, Eng, CM and USER coordination meetings.
• Management of CQV related documentation.

Skills

Bilingual (Spanish & English)

Writing general documentation

MS Office applications

Education

Bachelor’s Degree in Life Science or Engineering

Job description

FITS, LLC in Gurabo, Puerto Rico is seeking qualified candidates for Validation and Commissioning & Qualification support. The role requires a Bachelor’s Degree in Life Science or Engineering and expertise in the Validation Life Cycle within the Pharmaceutical Industry.

The candidate should be bilingual in Spanish and English and possess good documentation skills, along with experience in Process Commissioning and Validation coordination. Day-to-day responsibilities include project planning, coordination meetings, and management of CQV documentation.