Pharma Validation Specialist - On-Site in Juncos

INNOBAL CORP.; Juncos (PR); On-site; USD 70,000 - 100,000; Full time

Job summary

INNOBAL CORP. in Guaynabo, Puerto Rico, seeks a Validation Specialist for an on-site role in Juncos to plan, execute, and document validation activities for equipment, systems, and processes in pharmaceutical manufacturing.

You will prepare validation protocols and reports, perform testing and data collection, review results against acceptance criteria, and ensure compliance with cGMP, FDA/EMA expectations.

Qualifications

• Proficient in Computer System Validation including protocol development, execution, and documentation in regulated environments.
• Strong experience with Process Validation, including equipment qualification, process performance qualification, and ongoing verification.
• Knowledge of validation methodology, risk assessment, and maintaining validated status for systems and processes.

Responsibilities

• Plan, execute, and document validation activities for equipment, systems, and processes in pharmaceutical manufacturing facilities.
• Prepare validation protocols and reports; perform testing and data collection; review results against acceptance criteria.
• Ensure compliance with cGMP, FDA, EMA, and other regulatory expectations; support audits and change control.

Skills

Computer System Validation

Process Validation

Validation methodology

Quality Assurance

Regulatory compliance in pharma

English language proficiency

Education

Bachelor's degree in Engineering, Life Sciences, or related field

Tools

Validation software tools

Job description

INNOBAL CORP. in Guaynabo, Puerto Rico, seeks a Validation Specialist for an on-site role in Juncos to plan, execute, and document validation activities for equipment, systems, and processes in pharmaceutical manufacturing.

You will prepare validation protocols and reports, perform testing and data collection, review results against acceptance criteria, and ensure compliance with cGMP, FDA/EMA expectations.