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- ...Computer Systems Validation Specialist III Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and... ...Works independently and in teams. ~ Background in biotech, pharma, or medical device industry. ~ Ability to work independently...SuggestedRelocation package
Lonza
Dover, NH2 hours ago - ...Summary We are seeking a proactive Validation Engineer with in a regulated manufacturing environment (medical devices, pharma, or biotech, preferably FDA) to ensure compliance and drive operational integrity. This is an on-site position that focuses on equipment validation...Suggested
Creative Solutions Services, LLC
Tucson, AZ1 day ago $105.28k - $150.4k
Role Description The Computer System Validation (CSV) Lead is responsible for developing, executing, and maintaining the validation strategy for GxP-regulated computerized systems supporting manufacturing, laboratory, and quality operations. This role ensures that all...SuggestedFull timeAstellas Pharma
Remote1 day ago- ...designers/engineers and other project team members to plan, and complete tasks associated with commissioning, qualification and validation of new and modified equipment, facilities, utilities, product, processes etc. in line with project, operations and quality objectives...SuggestedContract workTemporary workMonday to FridayNight shiftWeekend work
PowerToFly
New York, NY1 day ago - ...Reporting to the Senior Manager, Facilities, Engineering and Validation, the Senior Validation Engineer role includes aspects of traditional... ...compliance at all times to ensure the release of Nestle pharma products to serve our patients. This is an exciting opportunity...SuggestedWork experience placement
PowerToFly
New York, NY3 days ago - ...Validation Engineer Responsibilities The Validation Engineer will provide validation, technical, and compliance oversight for Cell Therapy and Viral Vector manufacturing and laboratory equipment throughout the full equipment lifecycle. This role will work with the Manufacturing...SuggestedWork at officeFlexible hoursNight shift
Planet Pharma Group
Houston, TX1 day ago - ...positive impact on a global scale... About the Business Join our Pharma Services Group (PSG)—a global leader providing integrated drug... ...solid dose (OSD) manufacturing. Discover Impactful Work The Validation Manager (C&Q) will lead commissioning and qualification...SuggestedFor contractors
Avery Healthcare Group Ltd.
Greenville, NC3 days ago $76k - $103k
...in Hauppauge, NY, to ensure the compliance and performance of IT systems in a pharmaceutical manufacturing environment. You will validate IT systems, focusing on audit trails, data integrity, and GxP compliance. The ideal candidate has a Bachelor's in Life Sciences or...SuggestedFull timeCipla
Hauppauge, NY1 day ago- ...Description Job Description 0065V6421 CSV Engineer (Laboratory)/Validation Engineer 2 Consultant Please contact Amanda Mazza, amanda... ...ECQ or lab equipment qualification Experience in biotech, pharma, plasma, or manufacturing laboratory environments Prior...SuggestedFor contractorsLocal area
Two River Consulting Partners
Summit, NJ15 days ago - ...Cipla is hiring a QA Operations Specialist in Fall River, MA. The role involves ensuring product quality compliance and overseeing validation activities in a cGMP manufacturing environment. Responsibilities include reviewing and approving protocols, collaborating with...SuggestedFull timeRemote work
Cipla
Fall River, MA3 days ago - ...of the world’s toughest challenges. About the Business Join our Pharma Services Group (PSG)—a global leader providing integrated drug... ...environment. Discover Impactful Work As an Engineer II, Computer Systems Validation (CSV), you will support validation activities tied to...SuggestedInternshipWork at officeMonday to FridayFlexible hours
Dormont Manufacturing Company
Columbia, SC1 day ago - ...discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, we play a vital role in the... ..., come grow with August! August Bioservices is looking for a Validation Engineer team member that is passionate and driven regarding their...SuggestedContract workLocal area
August-Bioservices
Nashville, TN3 days ago $65k - $105k
...an experienced CSV Engineer to support the implementation and validation of ELLA and Synergy Neo2 laboratory instruments. The ideal candidate... ...ECQ or lab equipment qualification Experience in biotech, pharma, plasma, or manufacturing laboratory environments Prior...SuggestedTemporary workWork experience placementLocal areaVerista, Inc.
Summit, NJ23 days ago- ...Hi, My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Test Method Validation SME position right now. Please send me your updated resume if you have relevant experience and interested in this position...SuggestedContract work
- ...Job Description Job Description We are seeking a Senior Validation Engineer with solid hands-on validation experience and a collaborative... .... Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out...SuggestedContract workFor contractorsFlexible hours
Cellares
Bridgewater, NJ18 days ago - ...programs and manufacturing improvement plans related to product packaging Create test protocols and technical reports Qualify and validate new components, equipment, processes, and operations Lead technical initiatives, CAPA resolutions, and compliance projects...
MILLENNIUMSOFT
Warwick, RI2 days ago - ...Hi, My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Verification & Validation (V&V) Engineer position right now. Please send me your updated resume if you have relevant experience and interested in this...For contractors
- ...decades of manufacturing excellence by doing what others consider impossible. Position Overview We are seeking a highly motivated Validation Engineer onsite at one of our five sites: Cranberry Twp., Sturgeon Bay, WI, Suffield, CT, Staunton, VA or Cranston, RI sites, to...Full timeWork at officeShift work
Cadence Inc
Staunton, VA3 days ago - ...ingredients (API’s), other chemicals and manufacturing components (eg: vials, ampoules) of pharma products. Develop and Execute Validationlife cycle deliverables which include Validation plans, requirement specifications, Risk Assessments, test plans, (IQ, OQ, PQ) protocols...Immediate start
FATHOM LIFE SCIENCES & TECHNOLOGY SERVICES
Mcpherson, KS2 days ago $90k - $115k
...Validation Engineer Our client in Fairfield, NJ is looking for a Validation Engineer for a Full time position. Pay is $90-115K annually DOE. Responsibilities: ~ Responsible for Validation/PPAP Packages on new customer programs, as well as ensuring compliance...Full timeG.A. Rogers & Associates
Fairfield, Essex County, NJ2 days ago- ...Conceives, plans and executes manufacturing process validations plans and studies. Adhere to the Change Control and Design Control requirements. Create robust validation documents such as Master Validation Plans / Report, IQ, OQ, & PQ's. Lead the writing and execution...Work experience placementWork at officeLocal area
TechDigital Group
Los Angeles, CA3 days ago - ...We are looking for an experienced Validation Engineer with a strong background in the Medical Device industry to support validation and project execution activities. Key Requirements: bachelor's degree in mechanical engineering Prior experience in the Medical Device domain...
Creative Solutions Services, LLC
Salt Lake City, UT5 days ago - ...Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering...
Validation and Engineering Group, Inc
Allentown, PA5 days ago - ...Title: Validation Engineer Location: Northridge, CA Duration: 6 Month Job Description: The individual chosen for this position will primarily be responsible for closing out process validations of a pilot manufacturing line for next-generation subcutaneous glucose sensors...Immediate start
OPULENTSOFT LLC
Los Angeles, CA1 day ago $40 per hour
...Job Title: Validation Engineer (Contractor) Location: Summit – West, New Jersey Type: Contract Job Description: We are seeking a Validation Engineer with 4–7 years of relevant experience to support validation activities in a pharmaceutical/biotech environment. This role...Hourly payContract workFor contractorsWork at officeInteletech Global Inc.
Jersey City, NJ1 day ago- ...Summary We are seeking an experienced Validation Engineer to support pharmaceutical manufacturing and quality operations in Washington. The ideal candidate will have hands‑on experience in equipment, process, cleaning, and computerized system validation within a GMP‑regulated...
Creative Solutions Services, LLC
Bothell, WA3 days ago - ...Job Summary We are seeking a detail‑oriented Validation Engineer to support validation and calibration activities for critical pharmaceutical manufacturing and sterile processing equipment. This role requires strong expertise in regulatory compliance, including GMP and...
Creative Solutions Services, LLC
Waltham, MA3 days ago - ...Responsibilities Client is seeking validation consultants to support a 9‑month minimum onsite project in South Carolina. The consultants will support validation execution and gap assessments tied to equipment qualification, tank qualification, mixing studies, smoke studies...
Creative Solutions Services, LLC
Lafayette, IN1 day ago $26.58 - $44.3 per hour
...Role: Validation Engineer I Location: 1000 New Horizons Way, Vacaville, CA - 95688 Contract: 6+ Months - possibility for extension or FTE conversion Shift: M-F 8am - 4pm (including unpaid lunch 30 mins) 5x onsite Pay Rate: $26.58 - $44.30/Hour + Benefits Job Summary With...Contract workWork at officeShift workCreative Solutions Services, LLC
Vacaville, CA1 day ago$80k
...Cleaning Visual Inspection, Swabbing and rinse sampling of CIP systems or manufacturing equipment. Support authoring and execution of validation life cycle activities such as URS, Criticality Assessments, Risk Assessments, FAT, SAT, IOPQ, PPQ, CSV, CV, PV, Periodic Reviews...Work experience placementYoh,-A-Day-
Noblesville, IN3 days ago
