GMP CQV Project Lead for Biologics Facility On-Site
Verista
Verista is seeking a Project Manager SME to lead the C&Q delivery team for a GMP viral vector facility build-out in Devens, MA. You will manage staffing, scheduling, and governance across LVV drug substance manufacturing and drug product filling suites, ensuring alignment with turnover, commissioning readiness, and final qualification reporting. The role requires 8–12+ years in GMP CQV leadership, proven capital project delivery, and strong stakeholder management. #J-18808-Ljbffr Verista
- Verista is seeking a Senior CQV Engineer to lead C&Q deliverables for facilities, utilities, HVAC,... ...interfaces in a Devens, MA site. You will drive design review... ...compliance and timely project closeout. This on-site, full... ...years CQV experience in GMP environments and strong communication...WebsiteFacilitiesFull time
$107.8k - $168.01k
...Overview We are seeking a Project Manager SME to lead the C&Q delivery team for a GMP viral vector facility build‑out in Devens,... ...Own day-to-day CQV delivery Interface with... ...approval readiness Biologics/cell and gene therapy... ...startup Strong owner/site stakeholder...WebsiteFacilitiesFull timeTemporary work- ...Myers Squibb is seeking a Senior Manager for GMP Maintenance to lead the 24/7 maintenance team supporting the Devens Site Biologics Manufacturing Operations. This role involves ensuring operational readiness of GMP facilities and developing maintenance strategies to...WebsiteFacilities
$80.47k - $123.51k
...seeking a Senior CQV Engineer to lead C&Q deliverables and... ...coordination for facilities, utilities, HVAC,... .../utilities CQV in GMP manufacturing, preferably biologics, sterile, cell/gene... ...pharmaceutical capital projects Hands‑on HVAC/... ...ability to be on‑site, full‑time in...WebsiteFacilitiesFull timeTemporary workWork experience placement$120.37k - $145.86k
...Summary The Senior Manager, GMP Maintenance leads the 24/7 GMP Maintenance team that supports Devens Site Biologics Manufacturing Operations.... ...ensuring that GMP manufacturing facilities, systems, and equipment are... ...to cross‑functional project teams. Working knowledge of...WebsiteFacilitiesHourly payFull timeTemporary workSummer workLocal area- Verista, Inc. in Devens, MA is seeking a Senior CQV Engineer to lead commissioning and qualification for facilities, utilities, HVAC, and cleanrooms within GMP manufacturing. You will coordinate PSSR, TOP reviews, and turnover evidence while guiding cross‑functional teams...Facilities
$87.78k - $161.65k
...We are seeking a Lead Validation Engineer... ...portfolio of facility, utility, process... ...best practices, project objectives, and quality... ...system leads and CQV engineers,... ...Acceptance Testing (FAT), Site Acceptance... ...~15+ years in GMP CQV, ideally across biologics, viral vector, cell...WebsiteFacilitiesFull timeTemporary workWork experience placement- ...Myers Squibb EU Policy is seeking a Senior Manager, GMP Maintenance to lead the 24/7 team supporting Biologics Manufacturing Operations in Devens, MA. The role involves ensuring operational readiness of GMP facilities and developing maintenance strategies to maximize performance...Facilities
- ...Validation Engineer to plan, schedule, and track validation projects across GMP facilities and equipment. You will develop detailed protocols and... ...including SIP validation. You will generate documentation, lead validation reports, and support customers with technical insight...WebsiteFacilities
- A leading company in the pharmaceutical sector is seeking a Contractor Field QA Specialist at their Single Use Facility in Devens, MA. This role is responsible for ensuring quality compliance and oversees QA activities on-site. The ideal candidate will have a strong background...WebsiteFacilitiesFor contractorsNight shift
- Bristol Myers Squibb is seeking a Senior Manager, Project Management in Harvard, MA. The role involves managing complex projects throughout Devens Biologics, utilizing hands-on project management experience in the Pharma/Biotech sector. The successful candidate will demonstrate...
- ...manufactured products, and other GMP processes as required.... ...atypical events, assessing complex biologics manufacturing issues for forward... ...of the manufacturing facility and support areas. 4. Supports... ...compliance with corporate and site procedures, cGMP regulations,...WebsiteFacilitiesShift workWeekend work
$135.2k - $163.83k
The Senior Manager, Project Management will manage and... ...projects throughout Devens Biologics. With a breadth of... ...in support of specific site goals & objectives. The... ...meeting materials with/for lead as requested,... ...record. Understanding of GMP and FDA regulatory requirements...WebsiteHourly payFull timeTemporary workWork experience placementSummer workLive inFlexible hours- ...data analysis Familiarity with GMP documentation and electronic... ...based at Devens Cell Therapy Facility (CTF). This role is responsible... ...prevention and closure through site quality systems. Collaborate... ...degree in Science or Chemical/Biological Engineering. Minimum 0-2 years...WebsiteFacilitiesWork at office
$87.78k - $145.31k
Verista is seeking a Lead Validation Engineer to oversee CQV execution activities in Harvard, MA. The successful candidate will have over... ...and will lead teams to ensure compliance with GMP standards. This full-time on-site role offers a salary range of $87,780 to $145,30...WebsiteFull time$146.4k - $204.93k
...world's most exciting projects in a dynamic... ...and Qualification Lead - Pharmaceutical /... ...will support complex GMP capital projects,... ...workstreams supporting facilities, utilities,... ...construction, vendors, and site operations.... ...and gene therapy, biologics, advanced therapy...WebsiteFacilitiesFull timeTemporary workFor contractorsLocal area- ...Foreman to supervise craft workers at the Bristol-Myers Squibb Biologics Facility in Harvard, MA. This role involves ensuring safety compliance... .... The position requires physical endurance to meet job demands and manage site conditions. #J-18808-Ljbffr The Brock Group IncWebsiteFacilities
$101.01k - $122.4k
...otherwise, this role is "On‑Site" at the location... ...electrical elements of new projects including development... ...vendors and Third Party Facilities Management company.... ...site management and/or lead, working independently... ...facilities, as well as GMP experience. Effective...WebsiteFacilitiesFull timeTemporary workFor contractors$70.49k - $113.52k
Job Overview We are seeking a Senior CQV Engineer to lead C&Q documentation, vendor leveraging, walkdowns... .... This role requires a field‑capable biologics process equipment validation lead who... ...validation SME Location & Schedule On‑site, full‑time in Devens, MA. Salary...WebsiteFull timeTemporary work- ...organization at the Single Use Facility (SUF) in Devens, MA. The... ...productivity within the group or project. • Builds relationships internally... ...to also have knowledge of GMP Manufacturing operations and processes... ...improvement and enhance site quality system efficiencies. •...WebsiteFacilitiesFor contractorsWork experience placementMonday to Thursday
$110.2k - $151k
...Manager - Construction & Facilities About Us Founded in 201... ...diverse perspectives lead to better outcomes. Job... ..., MEP services, and site and civil work. Reporting... ...ensure on‑time, on‑budget project delivery. Key... ...structures (AIA, NEC, lump sum, GMP), MEP systems, and...WebsiteFacilitiesContract workFor contractorsFor subcontractorLocal area$35 - $45 per hour
...our Devens and North Andover Massachusetts facilities. Weekend and other overtime work is... ...program for both the Devens and North Andover sites. Responsible for all calibration... ...Cause process Perform duties according to GMP standards and internal Standard Operating...WebsiteFacilitiesFull timeLocal area- ...standardized solutions at any of their facilities regardless of physical... ...resources available at that site. We are seeking Support System... ...manufacturing operations in a GMP-regulated environment. You will... ...Manage continuous improvement projects. Be an ambassador who embodies...WebsiteFacilitiesLocal area
$70.49k - $118.06k
...complete documentation in compliance with GMP/GDP standards Work collaboratively with engineering... ...Engineering preferred) 3-8 years of CQV/validation experience Hands‑on experience... ...This role requires the ability to be on‑site, full‑time in Devens, MA. National (US)...WebsiteFull timeTemporary work- ...all materials and equipment at the job site Ensure that all equipment on the job site... ...use and care for all Brock and Client facilities and equipment Performs Quality Assurance... ...Location Information Bristol-Myers Squibb - Biologics Facility Location of Job: US:MA:Devens...WebsiteFacilitiesFull timeContract workFor contractorsWork at officeShift work
$89.39k - $108.32k
...solutions within the Devens Cell Therapy Facility. This role focuses on recipe authoring, troubleshooting... ...years of experience with MES systems in Biologics, Pharmaceutical, or Cell/Gene Therapy... ...specific benefits listed on our careers site may vary by job and location. For more on...WebsiteFacilitiesFull timeRemote workShift work- ...Role Description This is a full-time, on-site Warehouse Driver role based in Littleton, MA. The Warehouse Driver is responsible for... ...and unloading products to and from customer locations and branch facilities. Day-to-day tasks include assisting with shipping and receiving...WebsiteFacilitiesFull time
$43.27 - $53.49 per hour
...facets of assigned validation projects. Develop highly specific... ...Place (SIP) validation using biological indicators and projects... ...specialized knowledge or expertise (GMP manufacturing facilities and equipment, computerized... ...‑term relationships. On‑Site Expectations 100% on‑site...WebsiteFacilitiesHourly payWork at officeMonday to FridayShift workWeekend workDay shift- Peak Technologies is seeking a Senior Solutions Engineer to lead and manage complex projects across Littleton, MA and Eagan, MN, collaborating with the sales team to craft technology strategies and solutions. The role evolves toward specialist and post-sales focus, delivering...Website
$89.53k - $108.49k
...role maintains quality oversight, ensures GMP compliance, and supports real‑time quality... ...concerns. Train new team members on routine facility Quality tasks. Support return‑to‑service... ...QA review complies with corporate and site procedures, cGMP regulations, and industry...WebsiteFacilitiesFull timeMonday to FridayShift workAfternoon shift
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