Senior Validation Engineer with experience supporting commissioning, qualification, and validation activities for process equipment in GMP-regulated environments. Responsible for executing IQ/OQ ...

120 Amazon Senior Validation Engineer Jobs Hiring Near You
Senior Validation Engineer with experience supporting commissioning, qualification, and validation activities for process equipment in GMP-regulated environments. Responsible for executing IQ/OQ ...
Sr. Validation Engineer
Hillsboro, OR · On-site
The Sr. Validation Engineer will serve as a subject matter expert, support complex technical projects, and provide guidance to junior team members. KEY RESPONSIBILITIES (This list is not exhaustive ...
Sr. Validation Engineer
Hillsboro, OR · On-site
The Sr. Validation Engineer will serve as a subject matter expert, support complex technical projects, and provide guidance to junior team members. KEY RESPONSIBILITIES (This list is not exhaustive ...
Senior Validation Engineer
Bend, OR · On-site
The Senior Validation Engineer will be part of a cross functional team that will plan and execute commissioning/qualification (CQ) projects for equipment and critical utilities process, tech transfer ...
Senior Validation Engineer
Bend, OR · On-site
The Senior Validation Engineer will be part of a cross functional team that will plan and execute commissioning/qualification (CQ) projects for equipment and critical utilities process, tech transfer ...
Senior Validation Engineer with experience supporting commissioning, qualification, and validation activities for process equipment in GMP-regulated environments. Responsible for executing IQ/OQ ...
Senior Validation Engineer with experience supporting commissioning, qualification, and validation activities for process equipment in GMP-regulated environments. Responsible for executing IQ/OQ ...
Senior Validation Engineer with experience supporting commissioning, qualification, and validation activities for process equipment in GMP-regulated environments. Responsible for executing IQ/OQ ...
Senior Validation Engineer with experience supporting commissioning, qualification, and validation activities for process equipment in GMP-regulated environments. Responsible for executing IQ/OQ ...
Senior Validation Engineer with experience supporting commissioning, qualification, and validation activities for process equipment in GMP-regulated environments. Responsible for executing IQ/OQ ...
Senior Validation Engineer with experience supporting commissioning, qualification, and validation activities for process equipment in GMP-regulated environments. Responsible for executing IQ/OQ ...
Sr. Validation Engineer
Hillsboro, OR · On-site
The Sr. Validation Engineer will serve as a subject matter expert, support complex technical projects, and provide guidance to junior team members. KEY RESPONSIBILITIES (This list is not exhaustive ...
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Sr. Validation Engineer
Hillsboro, OR · On-site
The Sr. Validation Engineer will serve as a subject matter expert, support complex technical projects, and provide guidance to junior team members. KEY RESPONSIBILITIES (This list is not exhaustive ...
Senior Validation Engineer
Indianapolis, IN · On-site
$107K - $130K/yr
The Senior Validation Engineer will be responsible for the drafting and executing commissioning, qualification, and validation (CQV) documents and protocols which support the use of highly ...
Senior Validation Engineer
Indianapolis, IN · On-site
$107K - $130K/yr
The Senior Validation Engineer will be responsible for the drafting and executing commissioning, qualification, and validation (CQV) documents and protocols which support the use of highly ...
Senior Validation Engineer
Indianapolis, IN · On-site
$107K - $130K/yr
The Senior Validation Engineer will be responsible for the drafting and executing commissioning, qualification, and validation (CQV) documents and protocols which support the use of highly ...
Senior Validation Engineer
Indianapolis, IN · On-site
$107K - $130K/yr
The Senior Validation Engineer will be responsible for the drafting and executing commissioning, qualification, and validation (CQV) documents and protocols which support the use of highly ...
Senior Validation Engineer - Medical Devices Location: Silver Spring, MD (Onsite) Duration: 06 months contract (High potential for extension) Job Summary We are seeking a Senior Validation Engineer ...
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Senior Validation Engineer - Medical Devices Location: Silver Spring, MD (Onsite) Duration: 06 months contract (High potential for extension) Job Summary We are seeking a Senior Validation Engineer ...
Sr. Validation Engineer
San Diego, CA · On-site
The Sr. Validation Engineer will serve as a subject matter expert, support complex technical projects, and provide guidance to junior team members. KEY RESPONSIBILITIES (This list is not exhaustive ...
Quick apply
Sr. Validation Engineer
San Diego, CA · On-site
The Sr. Validation Engineer will serve as a subject matter expert, support complex technical projects, and provide guidance to junior team members. KEY RESPONSIBILITIES (This list is not exhaustive ...
Senior Validation Engineer
Bend, OR · On-site
The Senior Validation Engineer will be part of a cross functional team that will plan and execute commissioning/qualification (CQ) projects for equipment and critical utilities process, tech transfer ...
Senior Validation Engineer
Bend, OR · On-site
The Senior Validation Engineer will be part of a cross functional team that will plan and execute commissioning/qualification (CQ) projects for equipment and critical utilities process, tech transfer ...
The Senior Validation Engineer will be part of a cross functional team that will plan and execute commissioning/qualification (CQ) projects for equipment and critical utilities process, tech transfer ...
Quick apply
The Senior Validation Engineer will be part of a cross functional team that will plan and execute commissioning/qualification (CQ) projects for equipment and critical utilities process, tech transfer ...
Requirements: * Experienced Validation Engineer with either minimum 3 years experience or Sr. Validation Engineer with minimum 5 years experience performing Validation on aseptic liquid fill ...
Requirements: * Experienced Validation Engineer with either minimum 3 years experience or Sr. Validation Engineer with minimum 5 years experience performing Validation on aseptic liquid fill ...
Sr. Validation Engineer
Raleigh, NC · On-site
The Sr. Validation Engineer will serve as a subject matter expert, support complex technical projects, and provide guidance to junior team members. KEY RESPONSIBILITIES (This list is not exhaustive ...
Sr. Validation Engineer
Raleigh, NC · On-site
The Sr. Validation Engineer will serve as a subject matter expert, support complex technical projects, and provide guidance to junior team members. KEY RESPONSIBILITIES (This list is not exhaustive ...
Sr. Validation Engineer
Hillsboro, OR · On-site
The Sr. Validation Engineer will serve as a subject matter expert, support complex technical projects, and provide guidance to junior team members. KEY RESPONSIBILITIES (This list is not exhaustive ...
Sr. Validation Engineer
Hillsboro, OR · On-site
The Sr. Validation Engineer will serve as a subject matter expert, support complex technical projects, and provide guidance to junior team members. KEY RESPONSIBILITIES (This list is not exhaustive ...
Sr. Validation Engineer
San Diego, CA · On-site
The Sr. Validation Engineer will serve as a subject matter expert, support complex technical projects, and provide guidance to junior team members. KEY RESPONSIBILITIES (This list is not exhaustive ...
Sr. Validation Engineer
San Diego, CA · On-site
The Sr. Validation Engineer will serve as a subject matter expert, support complex technical projects, and provide guidance to junior team members. KEY RESPONSIBILITIES (This list is not exhaustive ...
Senior Validation Engineer
San Jose, CA · On-site
Senior Validation Engineer Location: Santa Clara, CA Duration: Full-time/Perm Responsible for developing and performing post-silicon validation tests using advanced high-speed test equipment and ...
Senior Validation Engineer
San Jose, CA · On-site
Senior Validation Engineer Location: Santa Clara, CA Duration: Full-time/Perm Responsible for developing and performing post-silicon validation tests using advanced high-speed test equipment and ...
Sr. Validation Engineer
Waukegan, IL · On-site
$60 - $75/hr
Position: Sr Validation Engineer Location: Waukegan, IL 60087 onsite 5 days a week Duration: 1 2+ months Pay Rate $60.00 -$75.00 per hour W2 + Benefits I am looking for a CQV Project Lead to ...
New
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Sr. Validation Engineer
Waukegan, IL · On-site
$60 - $75/hr
Position: Sr Validation Engineer Location: Waukegan, IL 60087 onsite 5 days a week Duration: 1 2+ months Pay Rate $60.00 -$75.00 per hour W2 + Benefits I am looking for a CQV Project Lead to ...
New
Sr. Validation Engineer
San Diego, CA · On-site
The Sr. Validation Engineer will serve as a subject matter expert, support complex technical projects, and provide guidance to junior team members. KEY RESPONSIBILITIES (This list is not exhaustive ...
Sr. Validation Engineer
San Diego, CA · On-site
The Sr. Validation Engineer will serve as a subject matter expert, support complex technical projects, and provide guidance to junior team members. KEY RESPONSIBILITIES (This list is not exhaustive ...
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Re-posted 11 days ago
Job description
Senior Validation Engineer with experience supporting commissioning, qualification, and validation activities for process equipment in GMP-regulated environments. Responsible for executing IQ/OQ protocols, equipment verification, temperature mapping, SIP/CIP validation activities, deviation support, and ensuring compliance with GMP/GDP standards while collaborating with Engineering, QA, and Operations teams.
Roles & Responsibilities:
- Execute Installation Qualification (IQ) and Operational Qualification (OQ) protocols for process equipment and utility systems.
- Perform drawing walkdowns, including P&ID reviews and system verification activities to ensure equipment installation compliance.
- Conduct equipment and component verification activities during commissioning and qualification phases.
- Support Management of Change (MOC) activities and perform weld verification as part of validation and compliance processes.
- Perform and support temperature mapping studies using data loggers and validation tools such as Ellab.
- Assist with Steam-In-Place (SIP) and Clean-In-Place (CIP) execution, cycle development, and validation activities.
- Identify, document, and investigate deviations encountered during qualification and validation activities.
- Ensure accurate, complete, and compliant documentation in accordance with GMP and GDP requirements.
- Collaborate cross-functionally with Engineering, Quality Assurance (QA), Manufacturing, and Operations teams to support project execution and validation deliverables.
- Support field verification activities and ensure validation activities meet regulatory and quality standards.
- Utilize validation lifecycle management systems such as eVal and support documentation management within validation systems.
- Participate in equipment startup, operational readiness, and continuous improvement initiatives for validated systems and processes
- Bachelor's degree in STEM, Biomedical Engineering, Chemical Engineering, or a related technical discipline preferred.
- 3-8 years of CQV (Commissioning, Qualification & Validation) and/or Validation Engineering experience in GMP-regulated industries.
- Hands-on experience executing validation activities for process equipment and utility systems.
- Strong understanding of GMP/GDP requirements and validation documentation practices.
- Experience with IQ/OQ execution, field verification, and equipment qualification activities.
- Proficiency with eVal validation management system; experience with ValGenesis is a plus.
- Exposure to temperature mapping activities and validation tools such as Ellab preferred.
- Experience working with bioprocess equipment including bioreactors, filtration systems, chromatography systems, and ultrafiltration (UF) preferred.
- Ability to support second-shift operations and weekend work as required.
About Katalyst Healthcares & Life Sciences
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Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.
Industry
Scientific research and development services
Company size
51 - 200 Employees
Headquarters location
South Plainfield, NJ, US