cqv - Boston, Massachusetts, United States

Seeking a CQV Engineer to support equipment commissioning qualification and validation activities in a cGMP/FDA-regulated manufacturing environment. · ...

+Job summary · CQV Engineer (Biotech/Pharma) · +ResponsibilitiesTroubleshoot and resolve all commissioning issuesGenerate the commissioning summary reports for all respective protocols.+Requires a bachelor's or master's degree in Scientific (Biotechnology) or Engineering (Mechani ...

Looking for a highly organized and assertive CQV Scheduler to manage schedules, track progress, and push teams to meet milestones in a regulated manufacturing environment. · Own and maintain CQV schedules in Smartsheet · Track task status, dependencies, constraints, and critical ...

We are looking for highly motivated and energetic individual to join our team as a CQV Consultant in Boston area, MA. · This job is located in the United States and only candidates eligible to work in the US for any employer will be considered. · We serve businesses in a wide ran ...

We are seeking a skilled EMPQ specialist to support CQV (Commissioning, Qualification and Validation) efforts focused on Environmental Monitoring Performance Qualification in a regulated pharmaceutical manufacturing environment. · ...

A leading life sciences organization is seeking a CQV Engineer / Senior Validation Engineer to support commissioning, · qualification, and validation activities for GMP manufacturing systems and equipment. ...

Arcadis seeks a CQV Engineer to support Commissioning, · Qualification, and Validation (CQV) activities for pharmaceutical/biotech clients. · The ideal candidate has experience in GMP environments, · expertise in commissioning, qualification, and validation processes, · and knowl ...

This is a contract role for a CQV Engineer responsible for commissioning qualification and validation activities related to manufacturing equipment and processes. · Strong expertise in commissioning qualification and validation of equipment and processes. · Familiarity with regul ...

Arcadis is seeking a CQV Engineer to support Commissioning Qualification and Validation activities for a pharmaceutical biotech client in Norton This role will be responsible for ensuring that equipment facilities utilities and systems comply with regulatory operational requireme ...

DPS is looking for a CQV Engineer to work at the Client facility or previously agreed upon location. · ...

Arcadis is seeking a CQV Engineer to support Commissioning, · Qualification and Validation (CQV) activities for a pharmaceutical/biotech client. · ...

The CQV Automation Engineer executes automation commissioning, · qualification,and testing activities in GMP biotech/pharmaceutical environments. · This role supports automated systems while ensuring compliance with cGMP,GDP,and regulatory standards. · ...

We are seeking a highly organized · CQV Scheduler to own scheduling, · tracking, · and follow-up for CQV activities in · a regulated manufacturing environment.Own and maintain CQV schedules using Smartsheet · Track task status, · dependencies, · constraints, · critical path · ...

The organization is seeking a mid-to-senior level Automation Engineer to support Opex and Capex projects in a pharmaceutical manufacturing facility. · ...

The organization is seeking a mid-to-senior level Automation Engineer to support Opex and Capex projects in a pharmaceutical manufacturing facility. · ...

+The CQV Project Scheduler will coordinate and oversee all Commissioning, Qualification, and Validation (CQV) activities for a biotechnology manufacturing site in Norwood, MA. · +Schedule CQV activities for utilities. · Develop execution strategies. · +, , Create weekly schedules ...

A leading life sciences organization is seeking a CQV Engineer / Senior Validation Engineer to support commissioning qualification and validation activities for GMP manufacturing systems and equipment. · Develop and execute IQ OQ and PQ protocols for manufacturing systems and equ ...

We are seeking a mid-to-senior level Validation Engineer to support both Opex and Capex projects in a pharmaceutical manufacturing facility. · Validation Execution & Documentation: Independently develop and execute Commissioning and Qualification (CQV) protocols including IQ, OQ, ...

We are seeking a mid-to-senior level Validation Engineer to support both Opex and Capex projects in a pharmaceutical manufacturing facility. · The role requires experience with automation commissioning and qualification of process equipment, · including operation within a plant a ...

We are seeking a mid-to-senior level Automation Engineer to support Opex and Capex projects in a pharmaceutical manufacturing facility, focusing on the commissioning, qualification, and optimization of automated process equipment and control systems. · ...