Senior Validation Engineer - GMP & SIP (On-Site)
Alcami Corporation
Alcami Corporation is seeking a Senior Validation Engineer to plan, schedule, and track validation projects across GMP facilities and equipment. You will develop detailed protocols and execute IQ/OQ/PQ testing on chambers, autoclaves, and related systems, including SIP validation. You will generate documentation, lead validation reports, and support customers with technical insight. The role requires 5+ years of validation experience, a technical or scientific degree, and strong writing and #J-18808-Ljbffr Alcami Corporation
$70.49k - $118.06k
...people and our capabilities. Senior Validation Engineer Responsibilities Execute IQ... ...tools Assist with SIP/CIP execution and cycle development... ...documentation in compliance with GMP/GDP standards Work... ...requires the ability to be on‑site, full‑time in Devens, MA. National...SeniorWebsiteFull timeTemporary work$43.27 - $53.49 per hour
Sr. Validation Engineer Location: US-MA-Pepperell At Alcami, we deliver... .... Job Summary The Senior Validation Engineer... ...Also, Steam in Place (SIP) validation using biological... ...or expertise (GMP manufacturing facilities... ...term relationships. On‑Site Expectations 100% on‑site...SeniorWebsiteHourly payWork at officeMonday to FridayShift workWeekend workDay shift$80.47k - $123.51k
...Job Overview We are seeking a Senior CQV Engineer to lead C&Q deliverables and... ...facilities/utilities validation lead who can work across construction... ...facility/utilities CQV in GMP manufacturing, preferably... ...requires the ability to be on‑site, full‑time in Devens, MA....SeniorWebsiteFull timeTemporary workWork experience placement- Verista is seeking a Senior CQV Engineer to lead C&Q deliverables for facilities, utilities, HVAC, cleanrooms... ..., and room interfaces in a Devens, MA site. You will drive design review, testing... ...requires 8-12+ years CQV experience in GMP environments and strong communication...SeniorWebsiteFull time
- Verista, Inc. seeks a Validation Engineer to own document and data control for the C&Q team, including repository structure... ..., and maintaining dashboards while ensuring GMP standards and electronic records compliance. On-site in Devens, MA with full-time commitment. #J-188...WebsiteFull time
- Bristol 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... ...leadership skills, and a bachelor's degree in Engineering or a related field. This position offers...SeniorWebsite
$70.49k - $113.52k
Job Overview We are seeking a Senior CQV Engineer to lead C&Q documentation, vendor leveraging, walkdowns... ...‑capable biologics process equipment validation lead who can own systems through... ...validation SME Location & Schedule On‑site, full‑time in Devens, MA. Salary National...SeniorWebsiteFull timeTemporary work- Job Summary Senior CQV Engineer / Senior Validation Engineer with experience supporting commissioning, qualification... ...activities for process equipment in GMP-regulated environments. Responsible... ...equipment verification, temperature mapping, SIP/CIP validation activities, deviation...SeniorShift workAfternoon shift
$120.37k - $145.86k
Job Summary The Senior Manager, GMP Maintenance leads the 24/7 GMP Maintenance team that supports Devens Site Biologics Manufacturing Operations. The role is accountable for day... ...organization within the Devens Site Engineering Department and for ensuring that GMP manufacturing...SeniorWebsiteHourly payFull timeTemporary workSummer workLocal area$70.49k - $113.52k
Job Overview We are seeking a Validation Engineer to own document and data control for the C&Q team,... ...Degree or equivalent required 5-10+ years GMP document control or validation document... ...and communication skills Location: on-site, full-time in Devens, MA. Salary...WebsiteFull timeTemporary work$87.78k - $140.22k
...Overview We are seeking a Computer Systems Validation / Data Integrity Lead to support... ...QSR documentation. Lead Validation Engineer Responsibilities Lead CSV/DI... ...closeout Ensure documentation aligns with GMP, data integrity, and site validation expectations Support...WebsiteFull timeTemporary workWork experience placement$87.78k - $161.65k
...Job Overview: We are seeking a Lead Validation Engineer to provide senior technical governance across the C&Q lifecycle... ..., Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), and... ...equivalent required ~15+ years in GMP CQV, ideally across biologics, viral...WebsiteFull timeTemporary workWork experience placement- ...Sr. Manufacturing/Assembly Process Engineer Develop the plans and work instructions for the successful handling, manipulation, guidance,... ...well as direct personnel performing the System Assembly during on-site work Requirements/Experience At least 2 years technical...SeniorWebsite
- Verista, Inc. seeks a Lead CQV SME to provide senior technical governance across the Commissioning, Qualification and Validation lifecycle for facilities, utilities, equipment, automation, and cleanrooms at Devens, MA. You will own qualification strategy, risk-based decisions...Senior
- A global leader in pharmaceutical manufacturing is seeking a Quality Assurance professional to serve as the site SME for cleaning validation. The candidate should have a minimum of 7 years of quality assurance experience and strong knowledge of regulatory guidelines. This...SeniorWebsite
- ...want to make a difference. Role: This role serves as the site SME for all cleaning validation and verification activities related to intermediate and... ...assurance experience with an undergraduate degree in engineering, science or related field. Minimum of 3 years of experience...Website
$46 - $51 per hour
...services firm providing CQV, validation, and compliance support, along... ...technical staffing for regulated GMP environments. Working across... ...regulated operations. As a Validation Engineer, you will work across... ...interface with, and host vendors on site. Champion qualification...WebsiteHourly payWork at office$145.47k - $176.27k
...Senior Principal Scientist, Analytical Chemistry Working with Us... ...Scientist will collaborate across BMS sites with functional Analytical... .... Experience with GMP and GLP requirements and risk... ...analytical method development, validation, and technical transfer. Experience...SeniorWebsiteHourly payFull timeTemporary workPart timeFor contractorsSummer workWork at officeRemote workFlexible hoursShift work- Verista is hiring a Validation Engineer for a full-time, on-site position in Devens, MA. The role requires expertise in executing IQ/OQ protocols and supporting... ...commissioning activities, ensuring compliance with GMP/GDP practices. Candidates must hold a Bachelor’s in a...WebsiteFull time
- 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...Senior
- Katalyst CRO is seeking a Senior CQV Engineer in Massachusetts. This role requires experience in commissioning, qualification, and validation of process equipment in GMP-regulated environments. Responsibilities include executing IQ/OQ protocols, conducting equipment verification...Senior
$21.54 - $25.41 per hour
...Job Title: Shipper/Receiver - Pharma/GMP At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines... ...work environment at varying environmental conditions. On-Site Expectations 100% on-site position. 1st Shift: Monday - Friday...WebsiteHourly payWork at officeMonday to FridayDay shift$101.17k - $151.75k
...Senior Manufacturing Engineer When you join Watson-Marlow Fluid Technology Solutions, a part of the Spirax Group, you will be integrated into... ...requests as needed to support expansion of Deven Manufacturing site. Work closely with Production to identify areas for...SeniorWebsiteApprenticeshipLocal area$100k - $145k
Senior Manufacturing Engineer Location: Ayer, MA Job Type: Full Time, On Site Pay Range: $100,000 to $145,000 Benefits: Health, Dental, 401K, generous PTO and more Job Summary Adecco Permanent Recruitment is partnering with a well-established manufacturer in the specialty...SeniorWebsitePermanent employmentFull time$92.2k - $115.3k
...opportunity for a dynamic, results-oriented Senior Supplier Program Manager (SPM) to join... ...programs. This position may be based on-site at our Syracuse, NY, Orlando, FL, or Quincy... ...experience working with Quality, Engineering, Finance, Manufacturing, and Program Management...SeniorWebsiteTemporary workFor contractorsWork experience placementFor subcontractorCasual workWork at officeLocal area$87.78k - $147.12k
...people and our capabilities. Job Overview We are seeking a Lead Validation Engineer to lead C&Q scope for drug product filling, isolator, and... ...solving abilities Location This role requires the ability to be on-site, full‑time in Devens, MA. Salary Range (USA) $87,780 - $147,1...WebsiteFull timeTemporary work- Bristol 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...Senior
- ...solutions. Essential Job Duties and Responsibilities Site subject matter expert on serialization functionality... ...using and with: DELMIAWorks (IQMS), or comparable ERP. Validated systems and procedures related to GMP. Integrations, specifically APIs. Manufacturing and...SeniorWebsite
$89.53k - $108.49k
Senior Specialist, Field Quality QA Operations Position: Senior Field... ...quality oversight, ensures GMP compliance, and supports real‑... ...review complies with corporate and site procedures, cGMP regulations,... ...Chain, Digital Plant, Site Engineering, and Manufacturing. Judgment...SeniorWebsiteFull timeMonday to FridayShift workAfternoon shift- Bristol Myers Squibb EU Policy is seeking a Senior Field QA Specialist in Harvard, Massachusetts. This role is critical for maintaining quality oversight and ensuring GMP compliance in manufacturing operations. You will be responsible for reviewing Manufacturing Batch...Senior
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Senior Validation Engineer - GMP & SIP (On-Site). Be the first to apply!
- validation engineer consultant
- analog mixed signal ams verification engineer
- computer validation engineer
- medical device validation engineer
- validation engineer
- computer system validation engineer
- process validation engineer
- entry level verification engineer
- quality validation engineer
- asic verification engineer


