CQV Engineer

CQV Engineer Job DescriptionWe are seeking an experienced CQV Engineer to join our team in Pennington, NJ. The ideal candidate will have a strong pharmaceutical background and be ready to work fully onsite.Key Responsibilities:Conduct commissioning, qualification, and validation activities for pharmaceutical manufacturing equipment and systems.Develop and...

CQV Engineer Job DescriptionADVENT Engineering is seeking a highly skilled CQV Engineer to join our team in Albany. As a CQV Engineer, you will be responsible for executing IC/OC commissioning protocols for fermenters and the CIP skid, troubleshooting and resolving all commissioning issues, and generating commissioning summary reports.Key...

Job Title: Lead CQV Engineer/AnalystVerista is seeking a highly skilled Lead CQV Engineer/Analyst to join our team. As a key member of our quality assurance team, you will be responsible for leading the commissioning, qualification, and validation (CQV) activities for our facilities and utilities.Key Responsibilities:Author and execute technical CQV...

CQV Engineer (Biotech)Location – AlbanyContract: 6 months with the possibility of extension.ADVENT Engineering is an engineering and consulting firm providing expertise to the pharmaceutical and biotechnology industries. Head-quartered near San Francisco, California, and with operations in the Eastern and Western US, Canada and Singapore, our company is...

Job OverviewVerista is seeking a highly skilled Lead CQV Engineer/Analyst to join our team. As a key member of our organization, you will be responsible for ensuring the quality and compliance of our products and processes.Key ResponsibilitiesDevelop and execute commissioning, qualification, and validation protocols for production equipment.Lead risk...

CQV EngineerStrictly No C2C ResponsibilitiesDevelop and execute Commissioning, Qualification, and Validation (CQV) protocols, including IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification).Support the qualification of equipment, utilities, and systems in pharmaceutical manufacturing facilities, including HVAC,...

Job Title: Validation EngineerLocation : New jerseyJob Type: Contract No C2C only w2 Responsible for validating equipment, processes, and systems in pharmaceutical manufacturing to meet regulatory requirements. Key responsibilities include:Conduct validation tests (IQ, OQ, PQ)Document validation protocols and reportsEnsure compliance with GMP and FDA...

About the RoleWe are seeking a highly skilled Lead CQV Engineer/Analyst to join our team at Verista. As a key member of our organization, you will be responsible for leading commissioning, qualification, and validation activities for our clients in the life sciences industry.Key ResponsibilitiesAuthor and execute technical commissioning, qualification, and...

PSC Biotech provides the life sciences with essential services to ensure that health care products are developed manufactured and distributed to the highest standards in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients success and you can be a part of our team s achievements. Employing a global team of skilled...

PSC Biotech provides the life sciences with essential services to ensure that health care products are developed manufactured and distributed to the highest standards in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients success and you can be a part of our team s achievements. Employing a global team of skilled...

Seeking a CQV Lead specializing in facilities and engineering to oversee the qualification of building utilities clean utilities and environmental systems. This individual will be responsible for developing and executing commissioning qualification and validation (CQV) protocols to ensure regulatory compliance and to ensure traceability to design...

Seeking a CQV Lead specializing in facilities and engineering to oversee the qualification of building utilities clean utilities and environmental systems. This individual will be responsible for developing and executing commissioning qualification and validation (CQV) protocols to ensure regulatory compliance and to ensure traceability to design...

About PSC BiotechPSC Biotech is a leading provider of life sciences services, dedicated to ensuring the highest standards of quality and compliance in the development, manufacturing, and distribution of healthcare products.Job SummaryWe are seeking an experienced Validation Project Engineer to join our team. As a key member of our CQV team, you will be...

PSCBiotech provides the life sciences with essential services toensure that health care products are developed manufactured anddistributed to the highest standards in compliance with allapplicable regulatory requirements.Ourgoal is to skyrocket our clients success and you can be a part ofour team s achievements. Employing a global team of...

Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on...

We are seeking a Senior Project Manager with extensive experience in managing CapEx projects within the pharmaceutical industry. The role involves overseeing project schedules budgets and reporting for a complex CQV initiative. The Project Manager will work closely with crossfunctional teams ensuring alignment with project milestones and regulatory...

We are seeking a Senior Project Manager with extensive experience in managing CapEx projects within the pharmaceutical industry. The role involves overseeing project schedules budgets and reporting for a complex CQV initiative. The Project Manager will work closely with crossfunctional teams ensuring alignment with project milestones and regulatory...

About the RoleWe are seeking a highly skilled Associate Project Engineer to join our team at Verista. As a key member of our organization, you will play a critical role in ensuring the quality and compliance of our documentation and validation processes.ResponsibilitiesManage validation documentation in automated systems, including document control and...

Job OverviewVerista is seeking a highly skilled Lead CSV Engineer/Analyst to join our team. As a key member of our automation and validation team, you will be responsible for authoring, editing, and executing technical commissioning, qualification, and validation documentation for standard equipment, systems, and software.Key Responsibilities:Develop and...

Job DescriptionVerista is a leading provider of innovative solutions and services to the life science industry. We empower growth and innovation within the scientific community by providing cutting-edge solutions that enable informed decision-making.As an Associate Project Engineer at Verista, you will play a critical role in ensuring the quality and...