Senior Cleaning Validation Engineer – Pharma CQV Lead

Weil Group, Inc; Juncos (PR); On-site; USD 90,000 - 130,000; Full time

Job summary

Weil Group, Inc. is seeking a CQV/Cleaning Validation Engineer to develop and execute Cleaning Characterization and Cleaning Verification for manufacturing equipment and process systems in a pharmaceutical setting.

The role requires strong validation experience, proficiency in TOC and microbiological testing, and ability to coordinate sampling and reports. You will review procedures, equipment drawings, and process recipes, perform field verifications, and support validation activities across

Qualifications

• Minimum B.S. in engineering or life sciences with pharma background.
• At least 5 years in pharmaceutical CQV/validation environments.
• At least 3 years in Cleaning Validation or Cleaning Verification.
• Familiarity with CIP systems, cleaning cycles, TOC and microbiology testing.

Responsibilities

• Develop Cleaning Characterization and Cleaning Verification docs and field activities.
• Prepare characterization protocols and final reports for cleaning processes.
• Review procedures, batch records, P&IDs, and process recipes for validation readiness.
• Coordinate sampling plans for TOC and microbiological surface testing.
• Perform or support swab sampling and sample collection per protocol.
• Review data against acceptance criteria and document discrepancies.
• Provide execution support during off-shifts or extended hours as needed.

Skills

CQV/Cleaning Validation experience

Pharmaceutical manufacturing knowledge

Documentation/Report writing

Cross-functional collaboration

Education

Bachelor's degree in Engineering, Chemistry, Microbiology, Biotechnology, Life Sciences, or related discipline

Tools

TOC analysis tools

PI Historian

Job description

Weil Group, Inc. is seeking a CQV/Cleaning Validation Engineer to develop and execute Cleaning Characterization and Cleaning Verification for manufacturing equipment and process systems in a pharmaceutical setting.

The role requires strong validation experience, proficiency in TOC and microbiological testing, and ability to coordinate sampling and reports. You will review procedures, equipment drawings, and process recipes, perform field verifications, and support validation activities across