validation engineer jobs in Cambridge, United States

We are seeking a detail-oriented Validation Engineer with around 3 years of hands-on experience to support validation activities across equipment processes utilities cleaning and computerized systems in a GMP-regulated environment. · ...

This role supports manufacturing and quality operations through execution of process equipment and test method validations. · Execute and support process and equipment validations including IQ OQ PQ FAT and SAT · ...

· Massachusetts, USA · On-site · Job Description · this time focus on Validation engineers with "Aseptic Process" or "APS" experience local to Massachusetts. You can include CQV in your search or a combination of "Commissioning" "Qualification" are other keywords you might see o ...

Position: Validation Engineer. · Must be experienced in computer system validation using GAMP 5 methodology. · ...

We provide a full spectrum of services including facilities utilities process and automation engineering top-tier quality compliance and regulatory affairs consulting and innovative recruiting solutions. · collaborate with Engineering QA Automation and construction teams to ensur ...

We are seeking a Senior Validation Engineer (CQV) with 5+ years of hands-on commissioning, qualification, and validation experience to support bio-pharmaceutical manufacturing projects.This is a field-based, execution-focused role supporting GMP facilities utilities process equip ...

We are looking for a highly motivated mid-level CQV engineer (5+ Years of Experience) with good interpersonal skills to join Omni as a C&Q engineer / consultant supporting our clients' project execution at their pharmaceutical manufacturing facility. · ...

We are looking for a highly motivated mid-level CQV engineer to join Omni as a C&Q engineer / consultant supporting our clients' project execution at their pharmaceutical manufacturing facility. · ...

The Validation Engineer III reports to the Manager of Validation responsible for performing validation in a GMP biotech manufacturing facility managing medium size validation projects and providing technical assistance to less experienced technicians/engineers.Development of Vali ...

Job Description · Omni Consulting Services LLC is a woman and minority-owned engineering and consulting firm. · We are looking for a highly motivated mid-level CQV engineer with good interpersonal skills to join Omni as a C&Q engineer / consultant supporting our clients' project ...

We are looking for a highly motivated mid-level CQV engineer (5+ Years of Experience) with good interpersonal skills to join Omni as a C&Q engineer / consultant supporting our clients' project execution at their pharmaceutical manufacturing facility.This position is a field-based ...

We are seeking a skilled Validation Engineer to join our team at Net 2 Source Inc. As a Validation Engineer, you will be responsible for estimation of testing efforts for each project/application and development of validation and testing strategies based on system risk, complexit ...

This is a consulting engagement with our direct client, a leading global bio-pharmaceutical company. · ...

HVAC validation engineer responsible for iq/oq/pq of hvac systems supporting pharmaceutical manufacturing labs and cleanrooms in compliance with cGMP FDA and ISO standards. · Perform HVAC IQ/OQ/PQ and cleanroom qualification. · Execute temperature humidity pressure and airflow ma ...

This role supports manufacturing and quality operations through execution of process, equipment, and test method validations. · The Validation Engineer will work closely with engineering, quality, and manufacturing teams to ensure compliant and efficient production processes in a ...

The Validation Engineer role performs equipment, utility, cleaning, sterilization, software and process validation activities to ensure compliance with company procedures and industry standards in support of Operations and Quality Systems for cell therapies products in a GMP biot ...

Support a multi-phase validation project involving the reconfiguration of manufacturing Suites 5 & 6 and implementation of Client production. · ...

This role performs equipment, utility, cleaning, sterilization and software validation activities to ensure compliance with company procedures. The candidate must have a Bachelor's Degree or equivalent work experience and 1-2 years of validation experience. · Perform hands on exe ...

The Software QA Engineer supports the team by ensuring the quality, · safety, and reliability of embedded and application software for advanced medical devices. · ...

We are looking for a highly motivated mid-level CQV engineer with good interpersonal skills to join Omni as a C&Q engineer / consultant supporting our clients' project execution at their bio-pharmaceutical manufacturing facility. · This position is a field-based, execution-orient ...