Top 3 Qualification & validation specialist (cqv) Jobs in Ponce Pr

Commissioning, Qualification & Validation Specialist (CQV)
ECHO Consulting Group —Villalba Municipio, PR
- Contract
- 5 years
- Engineering
- Senior level
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5d
Validation Specialist (Cleaning-In-Place)
Validation & Engineering Group, Inc —Juana Díaz, PR
- Extended hours
- 7 years
- Senior level
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Commissioning / Qualification / Validation Specialist
Salas O'Brien, Inc. —Columbus, OH
Must possess the technical aptitude to evaluate engineering documents including specifications, wiring diagrams, P&ID’s, HVAC / mechanical system drawings, and…
$90,000 - $100,000 a year
13d
CQV Specialist - Packaging Equipment
Pinnaql —New Albany, OH
Coordinate activities with engineering, quality assurance, validation, manufacturing, and vendors to ensure proper startup and qualification of packaging lines.
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Commissioning, Qualification & Validation Specialist (CQV)

ECHO Consulting Group -
Villalba Municipio, PR

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Job Details

Contract
5 days ago

Qualifications

Quality control corrective actions
Data integrity assurance
Biology
Content creation for technical audiences
5 years
Pharmaceutical regulatory compliance
Engineering
Technical writing experience within manufacturing
Production deviation management
Good documentation practices (GDP)
Corrective and preventive actions (CAPA)
GMP
Microbiology
Bachelor's degree in biology
Manufacturing facility experience
Bachelor's degree in engineering
Production validation processes
Quality risk management
Scientific protocols
Compliance documentation
Quality compliance management
Chemistry
Collaboration with manufacturing teams
Biomedical regulatory compliance
Commissioning phase involvement
Senior level
Bachelor's degree in microbiology
Field commissioning
Bachelor's degree in chemistry
FDA regulations

Full Job Description

ECHO Consulting Group is a leader in providing solutions for the pharmaceutical, biotechnology, medical devices, and food industries. ECHO Consulting Group delivers high-quality solutions in CQV, quality management, regulatory compliance, manufacturing support, and project management. We are committed to offering exciting career opportunities in a workplace that values trust, respect, teamwork, creative talent, enthusiasm, and diligence. We are looking for talented professionals who are passionate about quality, collaboration, and delivering results. We believe great talent deserves great rewards. That’s why we offer a competitive compensation package and professional development.

Summary of Role:

We are seeking Commissioning, Qualification, and Validation (CQV) professionals to support validation activities in a regulated pharmaceutical, biotechnology, or medical device manufacturing environment. This role is open to Engineers, Scientists, and Validation Specialists with experience supporting equipment, utilities, laboratory systems, or facilities qualification. The selected consultant will support protocol development, execution, and validation documentation, ensuring compliance with cGMP regulations and industry standards.

Responsibilities:

Support Commissioning, Qualification, and Validation (CQV) activities.
Develop, review, and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols.
Assist with equipment startup and commissioning activities.
Author and review validation documentation, including protocols, reports, and discrepancy resolutions.
Ensure compliance with cGMP regulations, FDA guidelines, and internal quality systems.
Participate in risk assessments and impact assessments related to validation activities.
Support change control, deviations, and CAPA investigations when required.
Collaborate with Engineering, Quality, Laboratory, Manufacturing, and Validation teams.
Ensure compliance with Good Documentation Practices (GDP) and data integrity principles.

Shift: Administrative (Available to work or provide support to a 24/7 manufacturing operation, as required)

Location: Multiple locations

Education: Bachelor’s degree in Engineering, Chemistry, Microbiology, Biology, or related scientific discipline.

Preferred Qualifications:

5+ years of experience in validation, commissioning, qualification, or regulated manufacturing environments.
Knowledge of cGMP regulations and validation lifecycle.
Experience supporting IQ/OQ/PQ execution or validation documentation.
Strong technical writing and documentation skills.

Equal Employment Opportunity

ECHO Consulting Group, Inc. is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status, or membership in any other class protected by federal, state, or local law.

We assure you that your opportunity for employment with ECHO Consulting Group, Inc. depends solely on your qualifications.

Quick Apply

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qualification & validation specialist (cqv) jobs in ponce pr

Commissioning, Qualification & Validation Specialist (CQV)

Validation Specialist (Cleaning-In-Place)

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