PR · On-site
We are seeking an experienced Validation Engineer. Objectives of this Role: * Write and execute, Installation Qualification (IQ), and Operational Qualification (OQ) protocols and Summary Reports ...
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PR · On-site
We are seeking an experienced Validation Engineer. Objectives of this Role: * Write and execute, Installation Qualification (IQ), and Operational Qualification (OQ) protocols and Summary Reports ...
PR · On-site
Validation Scientist to provide support to qualification/validation activities related to solid dosage form packaging equipment. Include preparation of (IQ/OQ/PQ) protocols for packaging equipment ...
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PR · On-site
Validation Scientist to provide support to qualification/validation activities related to solid dosage form packaging equipment. Include preparation of (IQ/OQ/PQ) protocols for packaging equipment ...
Validation Engineer
Ponce, PR · On-site
We are seeking Validation Engineers or Specialists to support Validation/Qualification activities in a Medical Devices manufacturing environment. Key Requirements: * Bachelor Degree in Engineering
Validation Engineer
Ponce, PR · On-site
We are seeking Validation Engineers or Specialists to support Validation/Qualification activities in a Medical Devices manufacturing environment. Key Requirements: * Bachelor Degree in Engineering
Education: Engineer, Science Related. IE Prefered Years of Experience: 3-5 Skills: Statiscal data Analyst and Six Sigma Green Belt Certified - Prefered Knolwlwdge in Validations Strategies ...
Education: Engineer, Science Related. IE Prefered Years of Experience: 3-5 Skills: Statiscal data Analyst and Six Sigma Green Belt Certified - Prefered Knolwlwdge in Validations Strategies ...
Validation Specialist PQ Focus (E-Beam, Isolators, Filling Equipment) Position Overview We are seeking agile and hands-on Characterization & Validation Scientists to support an accelerated project ...
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Validation Specialist PQ Focus (E-Beam, Isolators, Filling Equipment) Position Overview We are seeking agile and hands-on Characterization & Validation Scientists to support an accelerated project ...
Validation Specialist PQ Focus (E-Beam, Isolators, Filling Equipment) Position Overview We are seeking agile and hands-on Characterization & Validation Scientists to support an accelerated project ...
Validation Specialist PQ Focus (E-Beam, Isolators, Filling Equipment) Position Overview We are seeking agile and hands-on Characterization & Validation Scientists to support an accelerated project ...
Validation Engineer
Arroyo, PR · On-site
Kelly ® Engineering is seeking Validation Specialist for contract position at manufacturing client in Arroyo, Puerto Rico. If you're passionate about bringing the latest professional discoveries to ...
Validation Engineer
Arroyo, PR · On-site
Kelly ® Engineering is seeking Validation Specialist for contract position at manufacturing client in Arroyo, Puerto Rico. If you're passionate about bringing the latest professional discoveries to ...
Process Validation Specialist
Juncos, PR · On-site
Plan, coordinate, and execute validation activities for parenteral and aseptic manufacturing processes. * Prepare, review, and approve validation protocols, reports, and related documentation.
Process Validation Specialist
Juncos, PR · On-site
Plan, coordinate, and execute validation activities for parenteral and aseptic manufacturing processes. * Prepare, review, and approve validation protocols, reports, and related documentation.
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 ...
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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 ...
Coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning development and validation. Perform investigation of deviations / discrepancies. Responsibilities:
Coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning development and validation. Perform investigation of deviations / discrepancies. Responsibilities:
The Cleaning Validation Specialist will be responsible for developing, executing, and managing cleaning validation activities to ensure compliance with regulatory requirements and internal quality ...
The Cleaning Validation Specialist will be responsible for developing, executing, and managing cleaning validation activities to ensure compliance with regulatory requirements and internal quality ...
Jr. Validation Specialist
Humacao, PR · On-site
Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the project management involved. Position Summary The Jr ...
Jr. Validation Specialist
Humacao, PR · On-site
Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the project management involved. Position Summary The Jr ...
Jr. Validation Specialist
Humacao, PR · On-site
Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the project management involved. Position Summary The Jr ...
Jr. Validation Specialist
Humacao, PR · On-site
Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the project management involved. Position Summary The Jr ...
Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the project management involved. Position Summary The Jr ...
Quick apply
Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the project management involved. Position Summary The Jr ...
Position Overview We are seeking a Cleaning Validation Specialist to support critical manufacturing operations at the solid dosage manufacturing site. This role will play a key part in cleaning ...
Position Overview We are seeking a Cleaning Validation Specialist to support critical manufacturing operations at the solid dosage manufacturing site. This role will play a key part in cleaning ...
Validation Engineer/Specialist
Juncos, PR · On-site
We are seeking Validation Engineers or Specialists to support Validation/Qualification activities in a Medical Devices manufacturing environment. Key Requirements: * Bachelor Degree in Engineering
Validation Engineer/Specialist
Juncos, PR · On-site
We are seeking Validation Engineers or Specialists to support Validation/Qualification activities in a Medical Devices manufacturing environment. Key Requirements: * Bachelor Degree in Engineering
Coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning development and validation. Perform investigation of deviations / discrepancies. Responsibilities:
Coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning development and validation. Perform investigation of deviations / discrepancies. Responsibilities:
Cleaning Validation Specialist
Juncos, PR · On-site
Coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning development and validation. Perform investigation of deviations / discrepancies. Responsibilities:
Cleaning Validation Specialist
Juncos, PR · On-site
Coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning development and validation. Perform investigation of deviations / discrepancies. Responsibilities:
Review and validate extracted data to ensure accuracy, completeness, and alignment with site practices and documentation. * Perform detailed assessments to identify remediation scope across ...
Review and validate extracted data to ensure accuracy, completeness, and alignment with site practices and documentation. * Perform detailed assessments to identify remediation scope across ...
Review and validate extracted data to ensure accuracy, completeness, and alignment with site practices and documentation. * Perform detailed assessments to identify remediation scope across ...
Review and validate extracted data to ensure accuracy, completeness, and alignment with site practices and documentation. * Perform detailed assessments to identify remediation scope across ...
Validation information
What is a validation job?
A validation job involves verifying that products, processes, or systems meet specified standards and requirements. It often includes tasks such as testing, documentation, and compliance checks, especially in industries like pharmaceuticals, manufacturing, and technology. Skills in quality assurance, attention to detail, and familiarity with validation protocols are typically required.
What is the difference between Validation vs Quality Assurance?
| Aspect | Validation | Quality Assurance |
|---|---|---|
| Purpose | Ensures products meet specifications and intended use | Prevents defects through process improvements |
| Focus | Product-specific testing and verification | Process and system quality control |
| Activities | Design validation, process validation, equipment validation | Audits, process reviews, standards compliance |
| Timing | Before product release | Throughout production cycle |
Validation focuses on confirming that a product or process meets specified requirements before release, while Quality Assurance emphasizes maintaining quality standards throughout the production process to prevent defects. Both roles are essential in industries like pharmaceuticals and manufacturing, but they serve different stages of quality management.
What is the 3 month rule for jobs?
In validation roles, the 3 month rule often refers to a probationary period during which an employee's performance and fit for the position are assessed. This period typically allows employers to evaluate skills, adherence to procedures, and reliability before confirming permanent employment or considering further training. It is common for companies to set this timeframe to ensure quality and compliance in validation processes.
What jobs pay $10,000 a month without a degree?
Validation roles typically do not pay $10,000 a month without specialized skills or experience. High-paying jobs that can reach this level without a degree often include sales, real estate, or certain entrepreneurial ventures, but they usually require strong skills, certifications, or a proven track record. Most roles with such income levels rely on performance-based compensation rather than formal education alone.
What engineers make $500,000?
Senior engineers in specialized fields such as software, petroleum, or aerospace engineering can earn $500,000 or more annually, often through a combination of base salary, bonuses, and stock options. High-level roles typically require extensive experience, advanced skills, and sometimes professional certifications or advanced degrees.
What are the key skills and qualifications needed to thrive as a Validation Engineer, and why are they important?
To thrive as a Validation Engineer, you need a solid background in engineering or life sciences, with expertise in quality assurance and regulatory compliance. Familiarity with validation protocols, statistical analysis tools, and industry standards such as GMP, FDA, or ISO guidelines is essential. Strong analytical thinking, attention to detail, and effective communication skills help you identify issues and collaborate across teams. These abilities ensure that products and processes meet strict safety and quality requirements, minimizing risks and ensuring regulatory approval.
What are some common challenges faced by professionals in validation roles, and how can they be overcome?
Professionals in validation roles often face challenges such as tight project timelines, evolving regulatory requirements, and the need for meticulous documentation. Balancing thoroughness with efficiency is crucial, as validation processes must be both comprehensive and timely to support product launches or regulatory submissions. Effective communication with cross-functional teams, proactive planning, and staying updated with industry standards can help overcome these challenges and ensure successful validation outcomes.
What are validation jobs?
Validation jobs involve ensuring that products, processes, or systems meet specific requirements and function as intended. In industries like pharmaceuticals, biotechnology, and manufacturing, validation specialists test equipment, procedures, and software to guarantee quality and compliance with regulatory standards. These professionals document their findings and help identify areas for improvement, playing a key role in quality assurance. Validation jobs are essential for maintaining product safety, effectiveness, and meeting industry regulations.
What are the most commonly searched types of Validation jobs in Puerto Rico? The most popular types of Validation jobs in Puerto Rico are:
Contractor
Posted 14 days ago
Job description
As a global organization, PharmEng Technology has been providing quality services to leading manufacturers of the Pharmaceutical and Biotech industries since 1997. Our employees come from diverse backgrounds where we value unique talents and work together to support our clients. In addition, our consultants have extensive experience obtained from world-class organizations across the globe, and the development of our staff continues to grow PharmEng Technology.
We are seeking an experienced Validation Engineer.
Objectives of this Role:
- Write and execute, Installation Qualification (IQ), and Operational Qualification (OQ) protocols and Summary Reports including thorough resolution of protocol discrepancies.
- Assess potential sources of variation in materials, processes, facilities, equipment, products, and packaging processes that may impact consistent performance or product quality; where needed, design studies to characterize impact of identified sources.
- Maintain an up-to-date knowledge of validation requirements, practices, and procedures.
- Interpret existing Validation Plans and Project Plans and apply concepts to the task at hand.
- Working with a team to ensure all aspects of activity within the Process Development and Validation group adhere to required policies and procedures, including safety and training.
- Investigate/troubleshoot validation problems, as well as, conduct some statistical analysis of testing results.
Skills and Qualifications:
- Bachelor’s degree in engineering, life science discipline, or equivalent experience in the pharma/biotech industries.
- Highly capable of developing, executing, and reviewing validation life cycle protocols.
- Knowledge of validation principles, standard concepts, practices, procedures, and requirements in GMP regulated environments.
- Proven capability to assess processes, equipment, and products for sources of variation, ability to analyze data and reach appropriate conclusions, and to perform and appropriately document deviations and investigations.
- Experience with validation and working knowledge of production is a plus.
- Familiarity with FDA regulatory requirements for the Pharmaceutical/biopharmaceutical industry (i.e. GMP and GLP).
- Experience with Microsoft Office Suite.
- Experience Programing LabView require
PharmEng Technology is committed to attracting and retaining world-class employees valued for their contributions to achieving business objectives. PharmEng offers continuous career growth, competitive wages, travel opportunities, a team mentality that sets us apart from our competitors, and more!