CQV/Validation Engineer

Job Description:Same as the others except the GAMP 5 is only a plus but a big plus.CQV- equipment validation (Lab equipment).Robotic or control systems experience.URS, IQ/OQA plus is GAMP experience but not as important for the CQV.

Job Description:Same as the others except the GAMP 5 is only a plus but a big plus.CQV- equipment validation (Lab equipment).Robotic or control systems experience.URS, IQ/OQA plus is GAMP experience but not as important for the CQV.

Engineer, CQVPay Rate: 50-55 per hourNorwood, MAMonday - FridayContract to startB.S. in engineering, science, or an equivalent technical field.Minimum of one (1) year of relevant experience in a GCLP/GLP or CLIA/CAP environment is desirable.The Engineer I, CQV (Commissioning, Qualification, and Validation) will be responsible for delivering commissioning,...

Engineer, CQVPay Rate: 50-55 per hourNorwood, MAMonday - FridayContract to startB.S. in engineering, science, or an equivalent technical field.Minimum of one (1) year of relevant experience in a GCLP/GLP or CLIA/CAP environment is desirable.The Engineer I, CQV (Commissioning, Qualification, and Validation) will be responsible for delivering commissioning,...

Summary The CQV Engineer will report to the CQV Manager to execute Commissioning, Qualification and Validation activities for a client in the Boston, MA area. The ideal candidate will be responsible for executing CQV activities at the new facility and to collaborate with Global Engineering, Facilities Operations, GIS, QA and PMO throughout the life cycle...

At Verista, our team of over 600 professionals collaborates with leading organizations in the life sciences sector to address their operational challenges. Our mission is to foster growth and innovation within the scientific community, assisting researchers, institutions, and companies in tackling some of the most significant healthcare issues globally. We...

CQV Engineer (Biotech)Location – MAADVENT 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 involved in almost every facet of global pharmaceutical and...

CQV Engineer (Biotech)Location – MAADVENT 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 involved in almost every facet of global pharmaceutical and...

Summary Arcadis DPS Group Global is seeking a highly skilled CQV Engineer with specialized expertise in qualifying filling line isolators for biotech and pharmaceutical applications. The ideal candidate will play a key role in ensuring the reliability, efficiency, and compliance of the manufacturing processes by leading the qualification efforts for isolator...

Summary Arcadis DPS Group Global is seeking a highly skilled CQV Engineer with specialized expertise in qualifying filling line isolators for biotech and pharmaceutical applications. The ideal candidate will play a key role in ensuring the reliability, efficiency, and compliance of the manufacturing processes by leading the qualification efforts for...

Position Description: The CQV Engineer develops documentation for the Commissioning, Qualification, and Validation of pharmaceutical facilities, utilities, and equipment. These people are responsible for protocol writing and execution (field verification), and development of summary reports at client sites. Other responsibilities include planning /...

Welcome to the forefront of innovation in cutting-edge patient-centered treatments! We are seeking the best and the brightest to join our high-performing organization as a CQV Engineering Consultant . As a leader within the life science industry, we are constantly pushing the boundaries of what is possible and redefining the standards of excellence. Our...

This opportunity requires long-term relocation to the Copenhagen area in Denmark. Consultys provides work visa sponsorship for this position.Job Summary Join our team as a Lead CQV Engineer and contribute to the successful execution of commissioning and qualification activities for pharmaceutical/biotech manufacturing facilities. As a key member of our team,...

This opportunity requires long-term relocation to the Copenhagen area in Denmark. Consultys provides work visa sponsorship for this position.Job Summary Join our team as a Lead CQV Engineer and contribute to the successful execution of commissioning and qualification activities for pharmaceutical/biotech manufacturing facilities. As a key member of our team,...

CSV EngineerLocation: Boston/Rhode Island Key Responsibilities:Develop and implement Quality System documentation aimed at establishing effective validation practices within the organization.Create User Requirement Specifications (URS), Functional Requirement Specifications (FRS), Risk Assessments, Configuration Specifications, Design Specifications, and CSV...

CSV EngineerLocation: Boston/Rhode Island Key Responsibilities:Develop and implement documentation for Quality Systems aimed at establishing effective validation practices within the organization.Create User Requirement Specifications (URS), Functional Requirement Specifications (FRS), Risk Assessments, Configuration Specifications, Design Specifications,...

CSV EngineerLocation: Boston/Rhode Island Key Responsibilities:Develop and execute Quality System documentation aimed at establishing effective validation practices within the organization.Create User Requirement Specifications (URS), Functional Requirement Specifications (FRS), Risk Assessments, Configuration Specifications, Design Specifications, and CSV...

CSV EngineerLocation: Boston/Rhode Island Key Responsibilities:Develop and execute Quality System documentation aimed at promoting effective validation practices within the organization.Create User Requirement Specifications (URS), Functional Requirement Specifications (FRS), Risk Assessments, Configuration Specifications, Design Specifications, and CSV test...

Validation EngineerACADEMIC QUALIFICATIONS:Bachelor’s degree in a Science or Engineering discipline with 5 years relevant experience in computer system validation.TECHNICAL QUALIFICATIONS/KNOWLEDGE:• Experience computer systems supporting R&D functions like Clinical, Pharmacovigilance/Drug Safety, Medical Affairs, Supply Chain, Regulatory Affairs and...

This individual assures validation activities are performed in conformance with applicable Standard Operating Procedures (SOPs) client standards industry best practices and regulatory requirements. The individual performs validation program-related activities such as DQ COM IQ OQ PQ CQ RQ etc.Essential Duties and Responsibilities• Writes and...