Cleaning Validation SME — Digital Data Integrity

Techengpr; Carolina (PR); On-site; USD 70,000 - 90,000; Full time

Job summary

A leading pharmaceutical company in Puerto Rico is seeking a Cleaning Validation Specialist to support crucial manufacturing operations. The role involves executing cleaning validation programs, driving digital transformation initiatives, and enhancing data integrity practices. The ideal candidate should have 3–7+ years of experience in cleaning validation, strong technical skills, and be fully bilingual in English and Spanish. Join the team to contribute to high-impact initiatives and process improvements in a dynamic environment.

Qualifications

• 3–7+ years of experience in cleaning validation within pharmaceutical or regulated manufacturing environments.
• Strong knowledge of cGMP / FDA regulations.
• Experience supporting digital platforms or paperless validation systems.

Responsibilities

• Participate in Cleaning Validation team meetings and provide updates.
• Develop and execute cleaning validation protocols and reports.
• Support digital transformation efforts by transferring documents.

Skills

Technical expertise in cleaning validation

Strong communication skills in English and Spanish

Analytical skills

Problem-solving skills

Education

Bachelor’s Degree in Engineering, Chemistry, Microbiology, or related Science field

Tools

TrackWise

Veeva

Job description

A leading pharmaceutical company in Puerto Rico is seeking a Cleaning Validation Specialist to support crucial manufacturing operations. The role involves executing cleaning validation programs, driving digital transformation initiatives, and enhancing data integrity practices. The ideal candidate should have 3–7+ years of experience in cleaning validation, strong technical skills, and be fully bilingual in English and Spanish. Join the team to contribute to high-impact initiatives and process improvements in a dynamic environment.