Principal QA Validation Leader - GMP & Validation Expert
RoslinCT US
RoslinCT is seeking a Principal, QA - Validation to provide QA oversight of validation activities across facilities and equipment. The role requires extensive Quality Assurance experience in a GMP environment and hands-on validation knowledge per GAMP. You will collaborate cross-functionally to ensure compliance with cGMP and 21 CFR Part 11, mentor colleagues, and support Health Authority Inspections and client audits. #J-18808-Ljbffr RoslinCT US
- RoslinCT US in Hopkinton, MA, seeks a Principal, QA - Quality Systems to provide QA oversight of Quality Systems and Computer System Validation. The role focuses on review/approval of CSV... ...for computerized systems within a GMP environment. The ideal candidate has extensive...Principal
- RoslinCT is a world-leading cell and gene therapy CDMO seeking a Principal, QA - Validation to oversee validation activities for facilities and equipment in a GMP environment. The role involves review and approval of validation deliverables, governance of procedures, training...Suggested
- ...ability to impact patients. ACCELERATING YOUR FUTURE The Principal, QA - Validation is responsible for providing QA oversight of validation activities... ...candidate has extensive Quality Assurance experience in a GMP environment and experience in Validation in accordance with...PrincipalContract workFlexible hours
$169.3k - $250.53k
...silicon solutions for the growing data center, enterprise, wireless, and automotive compute markets. As a member of the Post-Silicon Validation team, you will have the opportunity to contribute to several areas of product development and validation including functional,...PrincipalPermanent employmentFull timeInternshipWork from home- ...patients. ACCELERATING YOUR FUTURE The Principal, QA - Quality Systems is responsible for providing... ...of Quality Systems and Computer System Validation. This includes supporting review and... ...Quality Systems experience in a GMP environment and experience in Computer System...PrincipalContract workFlexible hours
- ...investigations, deviations, CAPAs, change controls, and continuous improvement within GMP cell therapy operations. You will partner with Manufacturing, Quality Assurance, Validation, MS&T, and Supply Chain to ensure timely, compliant investigations and audit readiness;...
$94.57k - $135.1k
...System Administrator (SAP expert)About Astellas Astellas... ...configuration guides, validation protocols, SOPs, and... ...materials.Partner with IT, QA, and system vendors to... ....Strong knowledge of GMP, 21 CFR Part 11, and data... ...-minded life science leaders, all dedicated to improving...Worldwide$152k - $197k
...Senior Validation EngineerThe Senior Validation Engineer will work as part of a larger validation... ...:Serve as a validation technical leader, providing subject matter expertise in qualification... .../ inspections.Ensure training is kept in GMP compliant state.Accountable for managing...For contractorsLocal areaFlexible hours$89.9k - $143.8k
A leading biotech company in Marlborough, MA, is seeking an individual contributor to lead commissioning, qualification, and validation (CQV) activities in a cGMP environment. The ideal candidate will have a Bachelor of Science in Engineering and over 5 years of experience...$196k - $269.5k
...AI Development & Agent Ops — Senior Principal Software Engineer Why This Role This... ...Infrastructure Solutions Group is a global leader in Solutions, Storage, Compute, and... ...framework, including agent versioning, testing, validation, compliance reviews, deployment...Principal$120k - $155k
...future. Summary of job description: The Principal Associate I/II, Plant Quality Assurance (... ...responsibilities: Serve as the second shift QA lead working alongside manufacturing... ...actions (CAPA), change control records and validation documentation. Author/review/approve quality...PrincipalLocal areaFlexible hoursShift workAfternoon shift$204.9k - $303.25k
...new high-level technical workProvide leadership for a geographically dispersed team of verification professionals in pre-silicon validation of a highly complex SoC design. What We're Looking ForBachelor’s degree in Electrical engineering, Electronics, Computer engineering...PrincipalPermanent employmentFull timeInternshipWork from home- ...Senior Principal Digital Electrical EngineerCollins Aerospace, an RTX company, is seeking... ...validationExperience in Artwork (ODB++) validation and creating PWB/CCA drawing setsExperience... ...and elder care servicesTeladoc Medical Experts, second opinion programThis position is...PrincipalWork at officeRelocation
$161.5k - $209k
Hardware Principal EngineerHelp build Dell's ruggedized servers, purpose-engineered to run reliably in the extreme conditions of telecom... ..., lead the configuration, integration, and system-level validation that readies these platforms for telco deployment, and represent...PrincipalRemote workWorldwide$161.5k - $209k
...Join us and help build the future of enterprise technology as a Principal Engineer on our Hardware Engineering Team in Hopkinton,... ...design against the specified architecture, review the design and validation resultsSet standards and determine design targets for the product...Principal$152.3k - $225.44k
...place to thrive, learn, and lead. Your Team, Your ImpactAs a Principal Technical Engineer 3rd Party IP Engineer with Marvell, you’ll... ...stages of SoC development including defining core requirements, validating IP developer competence, overseeing core development, technology...PrincipalPermanent employmentFull timeInternshipWork from home- ...employees experience every day.As a Principal Clinical Quality Assurance... ...improvement of Clinical QA processes, audit procedures and... ...Good Manufacturing Practice (GMP) and Good Documentation Practice... ...As a global medical technology leader for more than 45 years, we advance...PrincipalHourly payLocal areaRelocationShift work3 days per week
- ...ambitions. About this role:The Principal Design Quality Assurance... ...Change, and Design & Usability Validation Plans. Leads the execution of... ...audit facing subject matter expert as required. Supports regulatory... ...a global medical technology leader for more than 45 years, we advance...PrincipalHourly payImmediate startRelocation packageShift work3 days per week
- Replimune Group, Inc. in Framingham, MA seeks a Principal Associate I/II, Quality Assurance to support GMP compliance and product disposition for BDS, DP, and FDP... ...and external facilities. You will collaborate with QA, QC, Regulatory, and Clinical teams, manage batch release...
- ...cleaning and sanitizing of the production facility and equipment Validate that work areas and equipment have been properly cleaned and... ...approve employee time records Ensure compliance with food safety, GMP, and company sanitation standards Troubleshoot sanitation,...Full timeAll shiftsShift workAfternoon shift
- Collins Aerospace is seeking a Senior Principal Systems Engineer for on-site work in Marlborough... ...and extensive experience across CONOPS, validation, and testing of ground and airborne... ...engineers while coordinating with IPT leaders and customers to ensure program success....Principal
- An educational institution for the deaf is looking for a Principal to lead and supervise teaching and learning at Walden School, a program for deaf youth. The role involves overseeing educational standards, facilitating student support, and ensuring collaboration with families...Principal
$132.4k - $251.6k
...Senior Principal Systems Engineer Collins Aerospace, an RTX company, is a leader in technologically advanced and intelligent solutions for the global... ...lifecycle solutions from CONOPS to Validation Act as a Subject Matter Expert within discipline with advanced to expert...PrincipalTemporary workWork experience placementWork at officeRemote workRelocation packageFlexible hours- ...to share with you. Must be able to read, write, speak and understand English Must be at least 18 years of age Must have a valid driver's license A clean driving record with no more than two moving violations or DUI's in the last three years The physical...Hourly payFull timeShift workWeekend work
- ...oversee the digital campaign lifecycle from setup through post-launch validation. You will ensure precise, compliant processes and collaborate... ...tentpole campaigns, campaign infrastructure, and post-launch QA while aligning with cross-functional partners. Boston/Wellesley...Full time
- Sanofi in Framingham, MA is seeking a Head of Quality Compliance to oversee GMP activities and compliance programs across site operations including Framingham Biologics, Biosurgery, and Northborough. The role leads a team to ensure readiness for inspections and drives continuous...
$120k - $155k
Job Title Principal Application Scientist Location Hopkinton Overview Revvity is a developer and provider of end‑to‑end solutions designed... ...running or programming liquid handlers. Design and execute validation test plans including processing samples and generating run...PrincipalFull timeWork at officeLocal area- ...organizational performance.As the Sr. Principal, Integrated Business Planning... ...with and influence leaders across the global organization... ...functional team of subject-matter experts from both business and... ...and system enhancementsDesign, validate, and deploy process improvements...PrincipalLocal areaWorldwide
- ...lead a cross-functional team of subject-matter experts from all GO sub-functionsCollaborate with... ...to be introduced, working with both business leaders on other transformation leads to reach alignment Design and validate proposed changes Develop communication tools and...PrincipalLocal areaWorldwide
$142.14k - $179.22k
...and be responsible for global GMP quality within our internal and... ...operations team from process validation (PPQ) into commercial drug product... ...., CMOs or CTOs). Provides QA review/approval of cGMP... ...with Quality Engineering. Expert knowledge and experience in leading...Work at officeFlexible hoursShift work
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