CQV Engineer - Westford

+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 ...

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

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. · ...

+Transforming patients' lives through science+ · +BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles.+ · +The Manager, Quality Engineeri ...

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 ...

We are seeking a talented individual to coordinate CQV activities for a biotech manufacturing site in Norwood, MA. · The ideal candidate has strong startup experience, deep understanding of GMP requirements, and proven ability to build integrated CQV schedules using industry tool ...

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 ...

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

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 · ...

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 an experienced Process Engineer to support the design of a new Oral Solid Dosage manufacturing facility. · Assist in the design of the new OSD facility and associated process equipment · Serve as the primary technical point of contact for equipment packages · ...

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 ...

This time focus on Validation engineers with Aseptic Process or APS experience local to Massachusetts. ...

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 ...

+This is a contract Project Scheduler for a biotech client located in the Norfolk County area. · +Schedule activities for utilities, equipment, automation, and process systems. · Develop, manage and schedule execution strategies... · ...

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. · ...

The Process Engineer will support a major capital project involving the design and construction of a new Oral Solid Dosage (OSD) manufacturing facility. · Collaborate with project stakeholders, equipment vendors, site engineering, and automation teams. · Develop equipment bid pac ...

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. · ...