CQV Engineer - Westford

Who We Are · We're Genesis AEC – an award-winning architecture, engineering, construction management, and CQV firm and a leader in the life sciences industry. Ranked #5 in Pharmaceutical Design by ENR magazine, we are designing and constructing facilities that advance worldwide h ...

· WHO WE ARE · We're Genesis AEC – an award-winning architecture, engineering, construction management, and CQV firm and a leader in the life sciences industry. Ranked #5 in Pharmaceutical Design by ENR magazine, we are designing and constructing facilities that advance worldwid ...

WHO WE ARE · We're Genesis AEC – an award-winning architecture, engineering, construction management, and CQV firm and a leader in the life sciences industry. Ranked #5 in Pharmaceutical Design by ENR magazine, we are designing and constructing facilities that advance worldwide h ...

The Role · The individual in this role leads commissioning, qualification, and validation (CQV) activities to ensure facilities, utilities, equipment, systems (FUSE), and analytical instruments remain in a qualified and compliant state within cGMP manufacturing environments. · Th ...

The Role · The individual in this role leads commissioning, qualification, and validation (CQV) activities to ensure facilities, utilities, equipment, systems (FUSE), and analytical instruments remain in a qualified and compliant state within cGMP manufacturing environments. · Th ...

The Role · The individual in this role leads commissioning, qualification, and validation (CQV) activities to ensure facilities, utilities, equipment, systems (FUSE), and analytical instruments remain in a qualified and compliant state within cGMP manufacturing environments. · Th ...

We're looking for a Manager, Quality Engineering to provide quality oversight of qualification and validation activities at our Cell Therapy Facility in Devens, MA. · Review and approve commissioning and qualification lifecycle documentation associated with manufacturing site fac ...

The Manager, Quality Engineering at the Cell Therapy Facility (CTF) in Devens, MA will be responsible for providing Quality oversight of qualification and validation activities. · ...

We're looking for an experienced Manager to lead our Quality Engineering team at our Devens Cell Therapy Facility in Massachusetts. As Manager of Quality Engineering you will provide quality oversight of qualification and validation activities for the facility's startup operation ...

Working with Us · Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production lin ...

Life Sciences CSV / CQV Practice Leader · Role Overview · This role is responsible for building and scaling an organic CSV and CQV practice focused on regulated life sciences environments. The position is designed for a senior validation leader who can establish a new capability ...

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 ...

+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 ...

The Manager Quality Engineering at Cell Therapy Facility will provide quality oversight qualification validation activities change control for startup continuing operations Devens MA facility including commissioning qualification validation CQV computer systems validation CSV pro ...

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 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 · ...

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

The Clean Room SME will support the design, startup, · and early operational readiness of GMP cleanroom environments within · an early-stage biopharma CMO.8+ years of experience supporting GMP cleanroom environments within biopharma, · biotech or pharmaceutical manufacturing. · S ...

Job summary · The Senior Project Manager provides high-level leadership and technical oversight for complex facility modifications, expansions, and new facility construction projects within pharmaceutical environments. · Act as the primary Verista representative supporting client ...

· 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 ...