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- Job-ID32464689Reference26-01010Remote50% Remote 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...SuggestedRemote work
- ...your potential? Join Team Novo Nordisk and help us make what matters.The PositionPlan, manage & perform low to moderately complex validation projects and activities. Support engineers with writing change requests and conducting/writing deviation investigations. Support...SuggestedWork at officeLocal area
- Computer Systems Validation EngineerLocation: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families... ...beneficial.CAPAs and deviations experience desired.Biotech/Pharma/Medical Device/Medical or biologics industry experience required...SuggestedFull timeRelocation package
- Computer Systems Validation (CSV) SpecialistLocation: Portsmouth, NH. Relocation assistance is available for eligible candidates and their... ...and managing CAPAs and deviations.Background in biotech, pharma, or medical device industry.Strong attention to detail and ability...SuggestedFull timeRelocation package
- Validation & Engineering Group, Inc. (V&EG) 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, Project Management...SuggestedWeekend work
- ...Job Description Job Description Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides... ...experience in validation, commissioning, or regulated biotech/pharma environments. ~ Basic knowledge of GMP and validation...Suggested
Validation & Engineering Group, Inc
New Albany, OH8 days ago - ...Posted: 2026-08-18Location: Vacaville, CaliforniaCompany: Planet Pharma GroupContact: ApplicationsEmail: ****@*****.***.... ...or equivalent regulations.Minimum of two years’ experience in Validation or equipment qualification is desired.Ability to make sound decisions...SuggestedWork at office
- ...biotechnology, or research labs, with a full‑time M-F schedule and potential evenings/overtime for project needs. Responsibilities span laboratory system implementation, validation/qualification support, and ongoing instrument system care. #J-18808-Ljbffr Yoh,-A-Day-SuggestedFull timeAfternoon shift
- ...into reality. We partner with scientists, physicians, biotech and pharma innovators, and patient communities — all united by one goal:... ...be part of something bigger than yourself.About The Role: As a Validation Engineer I, you will be responsible for the design,...SuggestedFull timeTemporary workWork at officeLocal area
- ...Novo Nordisk and help us make what matters. The PositionThis role supports our Finished Production area with a focus on review of validation activities. Ensures plant systems batch release, and/or relevant quality processes are compliant with regulations. Has product...SuggestedLocal areaMonday to Friday
- ...About the Company Stark Pharma Solutions Inc. is a global consulting and staffing partner established in 2014, serving the Pharmaceutical... ...specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project...Suggested
Stark Pharma Solutions Inc
Boston, MA2 days ago - ...ready to realize your potential? Join Team Novo Nordisk and help us make what matters.The PositionPlan, manage & perform laboratory validation activities. Routine review of laboratory validation procedures & completed validation protocols for accuracy, completeness &...SuggestedLocal area
- ...to pioneer and shape the future of PCI.Summary of Objective:The Validation Engineer IV performs an array of well-defined validation... ...’s talk futureEqual Employment Opportunity (EEO) Statement:PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We...SuggestedFull timeContract workWork experience placementWork at office
$70.92 - $99.29 per hour
...Validation Engineer 2 – CSV/CQV SpecialistLocation: 1201 NW Wall Street, Bend, OR 97703 Work Model: Full-Time, Onsite Contract Duration: 6–9 Months (Potential for Extension or Full-Time Conversion) Pay Rate: $70.92–$99.29/hour (W2) Benefits: Weekly Pay, Medical, Dental...SuggestedWeekly payFull timeContract workFor contractorsTailored Management
Bend, OR4 days ago- ...Validation Engineer IIThe CSV Engineer will, as an individual contributor, identify and implement industry best practices through an extensive... ...preferred. Prior experience leading projects in a Biotech/Pharma or biologics industry. Strong attention to detail and ability to...SuggestedWork experience placement
Ageatia Global Solutions
Portsmouth, NH13 hours ago - ...Job Title Validation - Engineer I / II - Project FarmaWhen joining PerkinElmer, you select an experienced and trusted leader in scientific... ...of equivalent work experience in capital project engineering, pharma cGMP facility start-up, CapEx/OpEx project management and/or comparable...Full timeWork experience placementWork visa
PerkinElmer
Portland, OR1 day ago - ...cGMP Quality Compliance Validation contract and perm MEDVACON Life Sciences works with many leading pharmaceutical companies to hire contractors... ...or biotech setting. Prior consulting exp in a cGMP setting in pharma or biotech in Quality, Compliance, Validation and/or CSV. NO...Permanent employmentContract workFor contractorsRemote work
MEDVACON
Edison, NJ5 days ago - ...Validation EngineerWe are seeking a proactive Validation Engineer with 1-3 years of experience 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...
Tranzeal
Tucson, AZ1 day ago - Be the First to Apply DivisionPiramal Pharma SolutionsPiramal Pharma Solutions is a contract development and manufacturing organization... ...worldwide. For more details, please visit : Job TitleEXPANSION Validation SpecialistJob DescriptionBusiness: Pharma SolutionsDepartment:...Contract workWork at officeWorldwide
$96k - $144k
...basis until the position is filled.What will you do?As an EMS Validation Engineering Lead, you will play a lead role in ensuring Schneider... ..., or a quality role within a GMP regulated environment (pharma) Four (4) Year engineering/technical degree in Pharmaceutical Manufacturing...Ongoing contractFull timeTemporary workWork at officeRemote workFlexible hours- ...$45 to $57/hr on W2 (depending on experience) Description: The Validation Specialist (Contract) will support pharmaceutical and medical device... ...PQ, requalification, and validation maintenance activities for pharma and medical device manufacturing systems. Support validation of...Contract workShift workWeekend work
Integration International Inc
Marion, NC5 days ago - ...operations within a GMP Final Drug Product (FDP) manufacturing environment. In this role, you’ll lead commissioning, qualification, and validation activities for new and existing equipment and processes, ensuring full compliance with FDA regulations and internal quality...Shift work
United Pharma
Brooklyn, NY2 days ago - ...Validation EngineerLocation: Vandalia, OhioSummary: In this position, the Engineer will utilize their formulations and/or technical services... ..., and the public.Works effectively under deadlines.Adare Pharma is an equal opportunity employer & prohibits unlawful discrimination...Contract workWork at office
Adare Pharma Solutions
Vandalia, OH1 day ago - ...integrations, and ensure data integrity and FDA 21 CFR Part 11 compliance. You will develop SOPs, train staff, map workflows, write test definitions, and collaborate with IT to validate and automate connections to analytical instruments. #J-18808-Ljbffr Hartmann Young
$85k - $100k
PSC Biotech® Corporation in Los Angeles is seeking experienced validation engineers to oversee the commissioning, qualification, and validation in the pharmaceutical and biotech sectors. The role emphasizes compliance with regulatory standards while ensuring documentation...- ...seeking a Chemist II to conduct analytical testing and method validation. Responsibilities include testing, protocol execution, and supervising... .... This role offers a competitive salary range and opportunities for professional development. #J-18808-Ljbffr Pyramid Pharma Services
- ...Job PostingJSat Automation is hiring a full time Validation Engineer with Pharma Industry experience. The Validation Engineer will be responsible for the following. Develop, approve, and execute process validation studies and protocols for cell and gene therapy manufacturing...Full time
E Tech Group
Glendale, CA1 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...For contractors
Avery Healthcare Group Ltd.
Greenville, NC2 days ago - Job-ID32783430Reference26-01356 Job Summary: A leading organization is seeking an experienced Pharma IT Testing & Validation Delivery Lead to manage global testing and validation services across multiple Life Sciences programs. Roles & Responsibilities: Own end-to-end...
$80k - $120k
Position: Computer System Validation/QC Informatics SpecialistSalary Range: $80,000 - $120,000/yr.Location: Coventry, RI (On-site)About PharmaronPharmaron... ...research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25...Contract workTemporary workWorldwideFlexible hours
