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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
Validation Specialist
Jayuya, PR · On-site
$60 - $80/hr
Support the design, implementation, troubleshooting, and validation of automation systems and ... Manage assigned deliverables to meet schedule, scope, and quality expectations. * Participate in ...
Validation Specialist
Jayuya, PR · On-site
$60 - $80/hr
Support the design, implementation, troubleshooting, and validation of automation systems and ... Manage assigned deliverables to meet schedule, scope, and quality expectations. * Participate in ...
Validation Specialist
Dorado, PR · On-site
For Validation services WHAT MAKES YOU A FIT: The Technical Part: * Bachelor's in Engineering with ... Document management systems The Personality Part: * Our Next Piece is someone who treats everyone ...
Validation Specialist
Dorado, PR · On-site
For Validation services WHAT MAKES YOU A FIT: The Technical Part: * Bachelor's in Engineering with ... Document management systems The Personality Part: * Our Next Piece is someone who treats everyone ...
Validation Engineer
Barceloneta, PR · On-site
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 ...
Validation Engineer
Barceloneta, PR · On-site
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 ...
Validation Specialist
Dorado, PR · On-site
$80 - $100/hr
For Validation services WHAT MAKES YOU A FIT The Technical Part: * Bachelor's in Life Sciences with ... Document management systems The Personality Part * Our Next Piece is someone who treats everyone ...
Validation Specialist
Dorado, PR · On-site
$80 - $100/hr
For Validation services WHAT MAKES YOU A FIT The Technical Part: * Bachelor's in Life Sciences with ... Document management systems The Personality Part * Our Next Piece is someone who treats everyone ...
Works with project managers and multidisciplinary teams to complete validation deliverables for engineering projects, facility modifications, capital projects, and new product introductions within ...
Works with project managers and multidisciplinary teams to complete validation deliverables for engineering projects, facility modifications, capital projects, and new product introductions within ...
Cleaning Validation Specialist
Juncos, PR · On-site
$60 - $80/hr
ECHO Consulting Group delivers high-quality solutions in CQV, quality management, regulatory ... Coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning ...
New
Cleaning Validation Specialist
Juncos, PR · On-site
$60 - $80/hr
ECHO Consulting Group delivers high-quality solutions in CQV, quality management, regulatory ... Coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning ...
New
Cleaning Validation Specialist
Jayuya, PR · On-site
The Cleaning Validation Specialist will be responsible for developing, executing, and managing cleaning validation activities to ensure compliance with regulatory requirements and internal quality ...
Cleaning Validation Specialist
Jayuya, PR · On-site
The Cleaning Validation Specialist will be responsible for developing, executing, and managing cleaning validation activities to ensure compliance with regulatory requirements and internal quality ...
Validation / CSV Specialist
Las Piedras, PR · On-site
$60 - $80/hr
Utilize Kneat to create, manage, execute, route, and maintain validation documents and records. * Support validation activities related to computerized systems, equipment, utilities, manufacturing ...
Validation / CSV Specialist
Las Piedras, PR · On-site
$60 - $80/hr
Utilize Kneat to create, manage, execute, route, and maintain validation documents and records. * Support validation activities related to computerized systems, equipment, utilities, manufacturing ...
Laboratory Validation Specialist
Anasco, PR · On-site
$80 - $100/hr
Computer System Validation (CSV), including ST and UAT execution ... Laboratory Equipment Qualification, Laboratory Instrumentation, and Equipment Lifecycle Management.
Laboratory Validation Specialist
Anasco, PR · On-site
$80 - $100/hr
Computer System Validation (CSV), including ST and UAT execution ... Laboratory Equipment Qualification, Laboratory Instrumentation, and Equipment Lifecycle Management.
Validation / CSV Specialist
Las Piedras, PR · On-site
$60 - $80/hr
Utilize Kneat to create, manage, execute, route, and maintain validation documents and records. * Support validation activities related to computerized systems, equipment, utilities, manufacturing ...
Validation / CSV Specialist
Las Piedras, PR · On-site
$60 - $80/hr
Utilize Kneat to create, manage, execute, route, and maintain validation documents and records. * Support validation activities related to computerized systems, equipment, utilities, manufacturing ...
Validation Engineer - Upstream
Manati, PR · On-site
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 ...
Validation Engineer - Upstream
Manati, PR · On-site
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 ...
Cleaning Validation Specialist
Jayuya, PR · On-site
$80 - $100/hr
Job Summary The Cleaning Validation Specialist will be responsible for developing, executing, and managing cleaning validation activities to ensure compliance with regulatory requirements and ...
Cleaning Validation Specialist
Jayuya, PR · On-site
$80 - $100/hr
Job Summary The Cleaning Validation Specialist will be responsible for developing, executing, and managing cleaning validation activities to ensure compliance with regulatory requirements and ...
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 ...
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 ...
Validation Engineer - Upstream
Humacao, PR · On-site
$80 - $100/hr
... Management, Validation, and other services. We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: Description We are seeking ...
Validation Engineer - Upstream
Humacao, PR · On-site
$80 - $100/hr
... Management, Validation, and other services. We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: Description We are seeking ...
Jr. Validation Specialist
Carolina, PR · On-site
$60 - $80/hr
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 ...
Jr. Validation Specialist
Carolina, PR · On-site
$60 - $80/hr
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 ...
Cleaning Validation Specialist
Carolina, PR · On-site
$80 - $100/hr
Document management systems (e.g., Veeva) * Experience supporting digital platforms or paperless validation systems is highly preferred. * Strong technical writing, analytical, and problem-solving ...
Cleaning Validation Specialist
Carolina, PR · On-site
$80 - $100/hr
Document management systems (e.g., Veeva) * Experience supporting digital platforms or paperless validation systems is highly preferred. * Strong technical writing, analytical, and problem-solving ...
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 ...
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 ...
Validation Manager information
What is a validation manager?
A validation manager works in a manufacturing plant and oversees the proper operation of machinery and equipment. Your job duties include developing operational plans for the entire facility, identifying areas of process improvement, and scheduling periodic auditing reviews of the facility. The qualifications needed for a career as a validation manager include a bachelor’s degree in business, organizational theory, quality control, or a related field. You also need strong communication and computer skills and experience in a management position.
What are the key skills and qualifications needed to thrive as a validation manager, and why are they important?
To thrive as a Validation Manager, you need a strong background in quality assurance, regulatory compliance (such as FDA or EMA guidelines), and validation principles, usually supported by a degree in life sciences or engineering. Familiarity with validation protocols, risk management tools, and systems like GMP documentation platforms is essential. Leadership, attention to detail, and effective communication are crucial soft skills for managing teams and coordinating cross-functional projects. These skills and qualities ensure that products and processes consistently meet regulatory standards, reducing risks and ensuring compliance.
How does a validation manager typically collaborate with other departments during project execution?
Validation Managers frequently work cross-functionally with quality assurance, manufacturing, engineering, and regulatory teams to ensure all systems and processes meet required standards. Effective collaboration involves coordinating validation protocols, sharing critical documentation, and communicating status updates to keep projects on track. A Validation Manager often leads meetings to align stakeholders, addresses compliance concerns, and resolves issues swiftly to prevent delays. Building strong relationships across departments is essential for smooth validation processes and successful project outcomes.
What is the difference between Validation Manager vs Quality Assurance Specialist?
| Aspect | Validation Manager | Quality Assurance Specialist |
|---|---|---|
| Certifications | GxP, ISO, or industry-specific validation certifications | ISO, Six Sigma, or QA-related certifications |
| Work Environment | Regulated industries like pharmaceuticals, biotech, or medical devices | Manufacturing, software, or service industries |
| Primary Focus | Ensuring validation processes for equipment, systems, and processes meet standards | Monitoring and improving overall quality processes and compliance |
The Validation Manager primarily oversees validation activities to ensure compliance with industry standards, focusing on equipment and process validation. In contrast, the Quality Assurance Specialist concentrates on maintaining overall quality standards across products and services. Both roles are essential for compliance but differ in scope and responsibilities.
More about Validation Manager jobs
What are the most commonly searched types of Validation jobs in Puerto Rico?
The most popular types of Validation jobs in Puerto Rico are:
What are popular job titles related to Validation Manager jobs in Puerto Rico?
For Validation Manager jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Validation Manager jobs in Puerto Rico look for?
The top searched job categories for Validation Manager jobs in Puerto Rico are:
Validation Specialist (Cleaning-In-Place)
Barceloneta, PR • On-site
Full-time
Re-posted 2 days ago
Key responsibilities
Review and approve vendor FAT/SAT protocols for CIP/SIP equipment.
Execute IOQ and PQ protocols for CIP/SIP systems, including cleaning recipe verification and sterilization cycle qualification.
Collaborate with cross-functional teams to ensure successful integration of CIP/SIP operations and support process validation activities.
Job description
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:
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:
Documentation & Compliance:
Cross-functional Collaboration:
Qualifications:
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.
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.