Validation Specialist (Cleaning-In-Place)

Veg Group; United States; Sur place; Plein temps

Avantages offerts par ce poste

Empowering work environment

Opportunity for professional development

Supportive team culture

Résumé du poste

A leading validation services provider in the United States is seeking a Validation Specialist to oversee Commissioning, Qualification, and Validation activities related to Cleaning-In-Place systems in biotech. The role requires a bachelor's degree in engineering and 7-10 years of CQV experience in pharmaceutical environments. Responsibilities include executing protocols, generating documentation, and ensuring compliance with industry standards. Strong skills in cleaning validation and proficiency in both English and Spanish are essential. This position offers an opportunity to make substantial contributions within a supportive team.

Qualifications

• 7–10 years of experience in CQV within biotech or pharmaceutical manufacturing environments.
• Strong knowledge of cleaning validation and sterilization principles.
• Expertise in ASTM E2500, ISPE Baseline Guides, and FDA/EMA guidelines.

Responsabilités

• Plan, coordinate, and execute all CQV activities related to CIP and SIP systems.
• Review and approve vendor FAT/SAT protocols for CIP/SIP equipment.
• Generate and review documentation in compliance with ASTM E2500 and GAMP 5.

Connaissances

Cleaning validation

Sterilization principles

Automation integration

Technical documentation

Bilingual (English/Spanish)

Formation

Bachelor’s degree in Chemical, Mechanical, or Biochemical Engineering

Outils

DeltaV

SCADA

PLC systems

Kneat

ValGenesis

Description du poste

Validation Specialist (Cleaning-In-Place)

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

• Validation Specialist - CIP

Summary

The Validation Specialist is responsible for planning, coordinating, and executing all Commissioning, Qualification, and Validation (CQV) activities related to Cleaning-In-Place (CIP) and Sterilization-In-Place (SIP) systems within a biotech manufacturing environment. This role ensures that cleaning and sterilization systems are installed, tested, and qualified in compliance with GMP, FDA, EMA, and ASTM E2500 standards, supporting readiness for process validation and commercial manufacturing.

Key Responsibilities

Commissioning & Qualification Execution

• Review and approve vendor FAT/SAT protocols for CIP/SIP equipment.
• Execute IOQ and PQ protocols for CIP/SIP systems, including cleaning recipe verification, steam sterilization cycle qualification, and temperature mapping.
• Oversee the qualification of utilities supporting CIP/SIP systems (Clean Steam, WFI, Process Air).
• Collaborate closely with Automation, Process, and QA Validation for recipe verification and data integrity.

Documentation & Compliance

• Generate and review URS, FAT/SAT, IOQ, and PQ documentation in compliance with ASTM E2500 and GAMP 5.
• Ensure traceability from design specifications through executed testing.
• Assist in managing deviations, non-conformances, and change controls related to CIP/SIP systems.
• Prepare summary reports for Quality Assurance approval.

Cross-functional Collaboration

• Collaborate with Process Engineers, Automation, QA, and Manufacturing to ensure successful integration of CIP/SIP operations with process equipment.
• Support operations during process validation batches and cleaning validation campaigns.
• Provide training and technical guidance to CQV engineers and contractors executing test protocols.

Qualifications

• Bachelor’s degree in Chemical, Mechanical, or Biochemical Engineering (or equivalent).
• Minimum 7–10 years of experience in CQV within biotech or pharmaceutical manufacturing environments.
• Experience in generating and executing documentation for CQV activities.
• Strong knowledge of cleaning validation, sterilization principles, and automation integration.
• Familiarity with DeltaV, SCADA, or PLC systems for CIP/SIP recipe management.
• Expertise in ASTM E2500, ISPE Baseline Guides, GAMP 5, and FDA/EMA guidelines.
• Proficiency in reviewing P&IDs, piping isometrics, and functional design specifications.
• Experience executing or overseeing FAT/SAT, IOQ, PQ activities.
• Knowledge of data integrity, 21 CFR Part 11, and electronic validation systems (e.g., Kneat, ValGenesis).
• Must be fully bilingual (English / Spanish) with excellent oral skills.
• Available to work extended hours, possibility of weekends and holidays.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Excited to build something meaningful together? We look forward to hearing from you.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.