Cleaning Validation Specialist

Job overview

The Cleaning Validation Specialist role is onsite in Indianapolis, IN. Compensation is not specified. The role supports cleaning validation programs for pharmaceutical and biopharmaceutical manufacturing operations. The specialist develops, executes, and maintains validation activities to verify that cleaning processes remove product residues, cleaning agents, and microbiological contaminants to scientifically justified acceptance criteria. The work supports compliant, documented, and consistently executed manufacturing cleaning processes.

What you'll do

• Develop and execute cleaning validation strategies, protocols, and reports
• maintain lifecycle documentation
• assess worst-case products and equipment
• establish acceptance criteria
• plan and coordinate swab and rinse sampling
• evaluate analytical results and perform validation calculations
• support CIP validation, process optimization, investigations, CAPA, change control, periodic review, audits, and regulatory inspections
• ensure GMP compliance.

What we're looking for

Skills & competencies

cleaning validation specialist

indianapolis in

proqualitynetwork

pharmaceutical manufacturing

biopharmaceutical manufacturing

gmp

cleaning validation protocols

swab and rinse sampling

cip validation

risk assessment

capa

3+ years experience

Work arrangement

• Weekend coverage required

Why this role

Requires a bachelor’s degree in a related scientific or technical discipline and 3+ years of relevant experience in a GMP-regulated manufacturing environment. The posting states that visa sponsorship is not available.

About the employer

ProQualityNetwork is hiring for this role. Industry: Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology). Sector: 54.