C&Q Specialist: GMP Validation & Commissioning

Veg Group; Puerto Rico; On-site; USD 70,000 - 90,000; Full time

Job summary

Validation & Engineering Group, Inc. in Puerto Rico seeks a C&Q Specialist to support commissioning and qualification activities for regulated pharma manufacturing environments.

You will develop and execute QC/validation protocols, coordinate field execution, and ensure documentation aligns with GMP and data integrity standards. Spanish and English communication is required; on-site work in the eastern region of Puerto Rico is expected.

Qualifications

• Minimum two years of C&Q, validation, startup or field execution experience.
• Bachelor’s degree in Engineering or Science is preferred.
• Experience with GMP documentation and tech writing is expected.

Responsibilities

• Support commissioning and qualification activities for capital projects.
• Prepare and execute protocols and related documentation.
• Coordinate field execution and startup support activities.
• Assist with deviations, punch lists and CAPA follow-ups.
• Maintain alignment with GMP, safety rules, and site procedures.

Skills

C&Q

Documentation

GMP

Data integrity (ALCOA)

Spanish language

English language

Education

Bachelor's degree in Engineering, Science, Business Administration, or related technical field

Tools

Kneat

Bluebeam

TrackWise

CMMS

Job description

Validation & Engineering Group, Inc. in Puerto Rico seeks a C&Q Specialist to support commissioning and qualification activities for regulated pharma manufacturing environments.

You will develop and execute QC/validation protocols, coordinate field execution, and ensure documentation aligns with GMP and data integrity standards. Spanish and English communication is required; on-site work in the eastern region of Puerto Rico is expected.