CSV Validation Specialist - GxP & Pharma Expert
Katalyst-Healthcares-
Requirements: Min 5 years of CSV experience. experience supporting validation of GxP GEN AI based solutions is a major plus experience supporting mergers/acquisitions/divestitures is a major plus Experience in the Pharmaceutical, biotechnology, or medical device industry Experience in FDA and/or Global regulated environment with good understanding of GxP standards and Risk based validation. Experience in writing and executing documentation for all aspects of the validation deliverables (etc. Requirements, Compliance/validation Plans, test protocols, Test Summary reports and Compliance/Validation Reports Experience in reviewing system test and user acceptance test scripts, Traceability matrix and Design Specs. Experience in QA Methodologies, designing, reviewing and approving Test Plans, System/UAT test scripts and Test procedures. Strong verbal and written communication skills. Ability to work as a team player, lead a team or accomplish tasks without supervision. Ability to work with remote teams and support several changes/projects simultaneously. Ability to provide Validation guidance, timely reviews, and escalations to TQ management. #J-18808-Ljbffr
- TechDigital Group in the United States is seeking a Validation Specialist with experience validating GEN AI solutions in GxP environments. The role focuses on supporting CSV AI projects and ensuring compliance with FDA and global regulations. You will write and execute...SuggestedRemote work
$65k
...Johnson is currently recruiting for QA Validation Specialist II LVV! .This position will be located in... ...Oversee Computerized System Validation (CSV) Must ensure that the selection, validation... ...computerized system used as part of the GxP regulated using the manufacturing area...SuggestedTemporary workLocal areaMonday to FridayShift workDay shift- ...Computer Systems Validation SpecialistDefine validation strategy for computerized systems and platforms utilized in GxP space.Create validation deliverables such as validation plan, test protocols, traceability matrix and execution of protocolsParticipate in user review...SuggestedRemote work
$55k - $70k
Baldwin & Obenauf, Inc. is seeking a proofreader in Somerville, NJ. The role demands 5+ years of experience, particularly in healthcare and pharmaceutical materials. As a key member of the team, you will ensure accuracy in editing across client communications, maintaining...SuggestedRemote jobFull timeContract workFreelance- ...Experienced Validation lead to support end to end validation ownership of a Unified Regulatory... ...management or Business Analysis in GxP application area Act as single point of accountability... ...guidance and support regarding SDLC and CSV processes, ensuring best practices are...Suggested
$87.1k - $94.6k
...done. We're obsessed with how it will be done.Key ResponsibilitiesCQV Execution & Safety- Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety- Deliver C&Q activities in alignment with project schedules- Track and report...For contractorsWorldwide- ...Bristol Myers Squibb is seeking a Senior Specialist, Operations Supply Planner for a 12-month assignment in New Jersey. The role partners with internal and external sites to develop and execute supply plans, balance service levels with efficiency, and manage MRP using...
- ...Legend Biotech is seeking a validation-focused professional to execute site validation activities, manage aseptic processing, and oversee equipment qualification ensuring alignment with regulatory requirements. You will collaborate with Manufacturing and Tech Support...
- Tris Pharma, Inc. in Monmouth Junction, NJ is seeking a Metrologist II to support analytical laboratories by calibrating and maintaining instrumentation such as HPLC/UPLC, UV-Vis, FTIR, and more under cGMP guidelines. The role involves collaboration with laboratory management...
- ...maintain GMP documentation, and follow SOPs and safety procedures to ensure compliant production. Requirements include 1+ year in pharma manufacturing, High School/GED, and Lean Six Sigma is a plus. The role offers an hourly rate with incentive opportunities. #J-18808...Hourly pay
- ...Work Order Management Expert, CMMS OperationsInsight Global is looking for a Work Order Management Expert, CMMS Operations to support one of our largest pharmaceutical clients within their cell therapy manufacturing team. This individual will own the weekly work management...
- ...We provide commissioning, qualification, validation, startup, project management, and other consulting... ...Documentation & Compliance Author GxP computer validation documentation (e.g.,... ...System & Industry Expertise Support CSV activities across various platforms...Worldwide
- ...Validation EngineerIntegrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce... ...has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors...
- ...Job TitleR3 Technology Inc. seeks Validation Engineer for its Hillsborough, NJ office.Responsibilities include gathering requirements to develop product-level requirements and assisting with the high-level systems view of product design. Conduct multi-disciplined product...Work at officeRelocation
- Recordati Rare Diseases, Inc. North America is seeking a Medical Science Liaison to serve as a field-based scientific expert focusing on Cushing's Syndrome, Cushing's Disease and Acromegaly. This role requires building peer-to-peer relationships with leading clinicians...
$160k - $220k
JobRx, Inc. is seeking a Medical Science Liaison (MSL) to build relationships with healthcare professionals focused on Cushing's Syndrome and related diseases. The role requires an advanced scientific degree and at least two years of experience in medical affairs. The MSL...- ...Job Description The Validation Engineer is responsible for executing, maintaining, and continuously improving site validation activities to ensure that equipment, utilities, facilities, processes, and systems remain in a qualified and validated state and comply with...
- ADESA, a Carvana-owned company, seeks a Title Administrator to process automotive titles in a customer-facing setting at our Manville, NJ site. You will greet visitors, assist with front-counter title needs, and verify title documentation for accuracy. Role requires DMV...
- Job Description Job Description Are You Ready? CAI is a professional services company established in 1996 that has grown to nearly 800 people worldwide. For mission-critical and regulated industries needing to deliver essential solutions in high-stakes environments...Worldwide
- H&R Block, Inc. is seeking a seasonal Experienced Tax Professional to assist clients with diverse tax situations, deliver personalized recommendations, and build lasting relationships. The role involves in-person work at a local tax office and participation in an industry...Seasonal workWork at officeLocal area
- A staffing agency is seeking an energetic warehouse worker in Bridgewater Township, New Jersey. The role involves receiving and dispatching merchandise, loading and unloading delivery vehicles, and ensuring a clean and safe work environment. Candidates should have experience...
- American Eagle Outfitters, Inc. in Bridgewater, NJ is seeking a part-time Brand Ambassador to create an exceptional in-store shopping experience. You will represent the brand, share product details, and drive loyalty program participation while maintaining brand standards...Part timeFlexible hours
- Advance Auto Parts is hiring a Retail Parts Pro in Flemington, NJ. This role supports advanced DIY services, sources parts, and uses store systems to assist customers with automotive needs. You will handle battery installations, tests, wiper installs, and related services...
- ...Colgate-Palmolive is seeking a Packaging Validation Engineer to lead global packaging test method strategy and to manage the Piscataway Packaging Lab. You will collaborate across Colgate's network to ensure validation frameworks support product innovation, quality, and...Worldwide
- Legend Biotech is seeking an Associate Manufacturing Engineer, Tech Support, based in Raritan, NJ, to support development and routine operation of a new CAR‑T manufacturing process. The role provides front line technical support to address manufacturing issues and ensure...Shift work
$99k - $148k
...with a clear case for production About you ~4 years building new manufacturing technology in chemicals coatings adhesives inks pharma advanced materials or a similar field in industry ~ A track record of introducing new manufacturing methods that has impacted...Full timeWork at officeWorldwideFlexible hours- ...Microchip Technology Inc. is seeking a senior engineer for functional validation focused on PCI Express and NVMe. The role involves pre-silicon and post-silicon validation of NVMe flash controllers, developing embedded software and drivers, and validating across hardware...
- ...KRG Technologies is seeking a Contract Commvault specialist for Branchburg, NJ. The candidate will work on Commvault 9, 10, and 11 with hands-on VSA and IntelliSnap backup restores. The role requires strong knowledge of live sync migration, backup failures, restore...Contract work
- Rutgers University invites applications for a faculty Hematopathologist at the Assistant Professor or Associate Professor level with responsibilities in hematopathology services for RWJ University Hospital in New Brunswick, NJ. The role includes consultation with clinical...
- ...: Quality Pro Services LLC is looking for a skilled Plumbing Expert to join our growing, family owned plumbing business in Middlesex... ...workmanship Ability to handle the physical demands of plumbing work Valid driver's license and clean driving record What We Offer:...Local area
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to CSV Validation Specialist - GxP & Pharma Expert. Be the first to apply!



