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Senior CQV Delivery Lead / Validation SME

Ayer, Massachusetts

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Today

Job Title Senior CQV Delivery Lead / Validation SME Job Location Devens MA -Onsite from day one -4x days on site / 1 remote (May go to 3 days once onboarded) -Need to be local OR WHO CAN RELOCATE FROM DAY ONE End Client BMS Duration - 6 Months+ Visa - Any Visa except H1B,CPT Mode Of Interview - Phone/Skype Note Need LinkedIn and we have to submit before end of the day. Provide senior technical governance across the C&Q lifecycle for a mixed portfolio of facility, utility, process

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Contract

Depends on Experience

Senior CQV Engineer/Senior Validation Engineer Consultant

Massachusetts

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Today

Job Summary: Senior CQV Engineer / 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 Qualif

Full-time

CQV System Lead - Viral Vector Process Equipment

Ayer, Massachusetts

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Today

Job Title CQV System Lead - Viral Vector Process Equipment Job Location Devens MA -Onsite from day one -4x days on site / 1 remote (May go to 3 days once onboarded) -Need to be local OR WHO CAN RELOCATE FROM DAY ONE Duration - 6 Months+ Visa - Any Visa except H1B,CPT Mode Of Interview - Phone/Skype Note Need LinkedIn Job description: Lead C&Q documentation, vendor leveraging, walkdowns, commissioning readiness, and qualification execution for viral vector drug substance process e

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Contract, Third Party

Depends on Experience

Senior Validation Engineer / Project Lead (Medical Devices)

Remote or Salt Lake City, Utah

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Today

Summary: We are seeking a highly skilled R&D/Validation Engineer with mandatory experience in the Medical Devices domain. The ideal candidate will be responsible for planning, leading, and coordinating project execution and validation activities in strict alignment with ISO 13485 and ISO 14971 standards. This role requires a hands-on leader who can manage equipment, process, and product transfers while liaising with global teams and customers to ensure on-time delivery. Roles & Responsibilities

Full-time

Lead Validation Engineer with Dspace

Remote

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30+d ago

Validation Lead with Some Sales experience Location - (Remote with Some travel in MI , TX , CA ) Expected Role: Collaborate with the sales team to understand client requirements and provide technical solutions around Network validation, HILs and fleet car testing solutions Assist in developing and executing strategic sales plans, focusing on the technical aspects of our products. Provide technical support to clients throughout the sales process, addressing inquiries

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Full-time

Depends on Experience

Verification Lead

Andover, Massachusetts

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20d ago

Required Qualifications Bachelor's degree in engineering, computer science, or a related technical field (or equivalent experience). 8+ years in verification, V&V, in medical devices. Demonstrated working knowledge of IEC 62304 (software lifecycle and safety classification) and ISO 14971 (risk management). Proficient in connected devices, embedded systems, or SaMD (Software as a Medical Device). Experience authoring verification plans and designing test protocols from requirements. Strong grasp

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Contract, Third Party

Depends on Experience

Senior Validation Engineer Consultant

Remote or Massachusetts

•

Today

Job Description: Senior CQV Engineer / 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 Q

Full-time

Senior CQV Engineer/Manager

Remote or Hybrid in Indianapolis, Indiana

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22d ago

Job Title: Senior CQV Engineer/Manager Location: Remote / Hybrid / Onsite (Depending on Project Requirements) Duration: Long-Term Contract Position Overview We are seeking an experienced CQV (Commissioning, Qualification & Validation) professional to support and lead validation activities within highly regulated pharmaceutical, biotechnology, and life sciences environments. This role will be responsible for ensuring GMP compliance across facilities, utilities, equipment, manufacturing processes,

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Contract

Depends on Experience

Senior Quality Validation & Compliance Manager

Remote or Hybrid in San Diego, California

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22d ago

Job Title: Senior Quality Validation & Compliance Manager Location: Remote / Hybrid / Onsite Duration: Long-Term Contract Position Overview We are seeking a highly experienced Senior Quality Validation & Compliance Manager to lead Quality Systems, Validation, Computer System Validation (CSV), Regulatory Compliance, and GxP initiatives within regulated Pharmaceutical, Biotechnology, Medical Device, and Life Sciences environments. The ideal candidate will possess extensive experience managing Qual

Easy Apply

Contract

Depends on Experience

Senior Virtualization Validation Engineer

Remote or San Francisco, California

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Today

Crusoe is on a mission to accelerate the abundance of energy and intelligence. As the only vertically integrated AI infrastructure company built from the ground up, we own and operate each layer of the stack - from electrons to tokens - to power the world's most ambitious AI workloads. When you join Crusoe, you join a team that is building the future, faster. We're in the midst of the greatest industrial revolution of our time. The demand for AI compute is boundless, and power is a bottleneck.

Full-time

USD 172,500.00 - 210,000.00 per year

Software Quality Engineering Lead

Remote or Santa Clara, California

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Today

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn m

Full-time

USD 187,000.00 - 207,000.00 per year

Senior Process Engineer – Chemical Manufacturing & Validation

Marlborough, Massachusetts

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13d ago

Seeking an experienced Process Engineer with 7+ years of experience in chemical manufacturing and GMP-regulated environments. The ideal candidate will lead equipment and process validations (IQ/OQ/PQ), support technology transfer and process scale-up activities, conduct risk assessments (HAZOP/FMEA), investigate process deviations, and drive continuous process improvements. Requirements: Bachelor''s degree in Chemical Engineering or related field710 years of chemical manufacturing experienceExpe

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Contract

Validation Engineer

Waltham, Massachusetts

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Today

Job Summary: We are seeking a detail-oriented Validation Engineer to support validation and calibration activities for critical pharmaceutical manufacturing and sterile processing equipment. This role requires strong expertise in regulatory compliance, including GMP and 21 CFR Part 11, along with hands-on experience in equipment qualification and computerized system validation (CSV). Roles & Responsibilities: Perform validation and calibration activities for pharmaceutical manufacturing and s

Full-time

Hardware Verification & Validation Engineer

Burlington, Massachusetts

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5d ago

Job Overview: The Hardware Verification & Validation Engineer, under general direction, will scope, define, develop, analyze and supervise tests for appliance components, subsystems or products. The Hardware Verification & Validation Engineer will collaborate with multi-functional team members and assume responsibility for developing design validation plans, test protocols, and test equipment for both new product development and improvement of existing product lines. The Hardware Verification &

Full-time

USD 76,400.00 - 105,000.00 per year

Process Validation Engineer

Remote or Bloomington, Indiana

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Today

Roles & Responsibilities: Bachelor's degree in Engineering, Science, or related field. Experience with equipment qualification, validation, or regulatory compliance. Familiarity with Kneat digital platform or similar document management systems. Strong understanding of CSV (Computer Systems Validation) principles. Knowledge of temperature mapping methodologies. Familiarity with Ellab systems or similar validation equipment.

Full-time

Lead Validation Engineer

Remote or New Jersey

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Today

Job Description: The Lead Validation Engineer leads GMP equipment installation, commissioning, and qualification projects supporting large-molecule biologics manufacturing. This role supports upstream and downstream processes and ensures projects are executed safely, on schedule, and in compliance with regulatory and quality requirements. Responsibilities: Lead end-to-end CQV execution for GMP equipment projects, managing activities from installation through IQ, OQ, and PQ for biologics manufact

Full-time

Atlassian Developer Data Validation & Testing

Remote

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22d ago

Atlassian Developer Data Validation & Testing Location: Remote | Type: Contract | Exp: 8 12+ Years Atlassian Developer focused on migration data validation and testing. Key Skills: Jira DC, Jira Cloud, Data Validation, Schema Mapping, Migration Testing, QA, Jira Configurations Role: Perform data validation during migrationExecute schema mapping (DC to Cloud)Test migrated configurationsEnsure data integrity

Easy Apply

Contract, Third Party

Depends on Experience

Senior Validation Engineer

Remote or Rock Hill, South Carolina

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Today

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

Full-time

Senior Engineer, Process Validation

Remote

•

Today

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the spee

Full-time

USD 100,000.00 - 130,000.00 per year

Process Validation Engineer

Remote or Indianapolis, Indiana

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Today

Job Description: We are seeking a Process Validation Engineer to support validation and qualification activities in a GMP-regulated manufacturing environment. The ideal candidate will have experience with process validation, equipment qualification, CSV, temperature mapping, and regulatory compliance. Responsibilities: Execute process validation and equipment qualification activities (IQ, OQ, PQ, PPQ). Develop, review, and maintain validation protocols and reports. Support Computer Systems Vali

Full-time

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