12 validation opportunities in Raritan updated today
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Summary: We are seeking a talented Validation Engineer to join our team. As a Validation Engineer, you will play a crucial role in ensuring the quality and compliance of our manufacturing processes and systems. You will be responsible for designing, implementing, and executing validation protocols t
Role: Life Sciences : Computer System Validation Engineer Location: Raritan, N Experience: 8 & Above Duration: 12+ Months Rate $50 - $55/hr(c2C) Must Have: Life Sciences : Computer System Validation Software Product Development GxP experience is required Role Descriptions: Demonstratable Experience
Role 1 : Jr. IM Regulatory Validation Lead Location: Raritan, NJ (Hybrid) Hire Type : Contract Job Description Technical Lead is responsible for end-to-end technical ownership of a Unified Regulatory Platform (URP) built on Veeva and AWS based cloud stack 1. Work with cross functional team 2. Ensure
Johnson and JohnsonAt Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine
Supporting and Validating Regulatory systems like REMS RIMS 10+ years experience in Computer System Validation of Regulatory systems like Regulatory Information Management System, REMS, Publishing, eCTD systems used in Pharmaceutical industry. Guide the project team with the right set of applicable
An established industry player seeks a seasoned professional with over a decade of experience in Computer System Validation within the Pharmaceutical sector. This role involves supporting and validating critical regulatory systems, guiding project teams through the SDLC process, and ensuring complia
ob Title: IM Regulatory Validation Lead Location: Raritan, NJ (Hybrid) Job Details: Experienced Validation lead to support end to end validation ownership of a Unified Regulatory Platform (URP) built on Veeva and AWS based cloud stack 8+ years experience in Computer System Validation or Quality mana
Legend Biotech USLegend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen
Job Title: IM Regulatory Validation Lead Location: Raritan, NJ (Hybrid) Job Details: Experienced Validation lead to support end to end validation ownership of a Unified Regulatory Platform (URP) built on Veeva and AWS based cloud stack 8+ years experience in Computer System Validation or Quality man
HPTech Inc.Senior Technical Lead Job Title: IM Regulatory Validation Lead Location: Raritan, NJ (Hybrid) W2/C2C Job Details: Technical Lead is responsible for end-to-end technical ownership of a Unified Regulatory Platform (URP) built on Veeva and AWS based cloud stack 1. Work with cross functional team 2. Ens
Requirements Must have: - Proven experience in Computer System Validation (CSV) - Familiarity with software development life cycle (SDLC) and software testing life cycle (STLC) - Proficient in drafting, reviewing, revising, and maintaining validation documents including Compliance Analysis, Complian
Sierra Business Solution LLCJob Title: Validation Lead with AI knowledge Location: Raritan, NJ Remote for Canada Type: Contract Role Descriptions: Demonstratable Experience in Computer System Validation (CSV)Experience in software development processes (SDLC) and software testing life cycle (STLC) Experience in drafting review
Validation Specialist Job Number: 26-00778 Be part of a company that delivers life-changing healthcare solutions. ECLARO is looking for a Validation Specialist for our client in Lawrenceville, NJ. ECLARO’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affor
Sr. CQV Specialist Position Summary We are seeking an experienced Sr. CQV Specialist to support commissioning, qualification, and validation activities within a cGMP Clinical and Commercial Cell Therapy Manufacturing facility. This role will support day-to-day CQV operations for facility, equipment,
Summary: Writing and execution of validation protocols and reports (i.e. IQ, OQ, PQ, etc.) Developing and implementing manufacturing processes, preparation of specifications and operator instructions, process studies, production readiness, investigations, root cause analysis, problem solving and rep
Validation Engineer Looking for a Validation Engineer in Middletown, VA. Launch your career with Our Client, a global scientific leader! You'll need a relevant Bachelor's degree and 0-2 years of regulated industry experience to drive critical validation efforts. Join us and make an impact!
Validation Engineers Metuchen, NJ & other unantcptd locns nationwide. Duties: Analyze validation test data to determine whether systems or processes have met validation criteria & to identify root causes of problems for various pharma & other facilities. Prepare validation & performance qualificatio
Made ScientificAbout Made Scientific Made Scientific is a leading US-based cell therapy contract development and manufacturing organization (CDMO) specializing in the development, manufacturing, and release of autologous and allogeneic cell therapy products for clinical-and-commercial supply. Made Scientific combi
Orion Innovation is a premier, award-winning, global business and technology services firm. Orion delivers game-changing business transformation and product development rooted in digital strategy, experience design, and engineering, with a unique combination of agility, scale, and maturity. We work
WuXi BiologicsJob Title - Validation Intern Work Location - Cranbury NJ (Onsite) About Us Welcome to the epicenter of innovation in healthcare! At Wuxi Biologics MFG18, in Cranbury New Jersey, we're not just about making medications; we're on a mission to rewrite the future of medicine. Picture a place where scie
AA2ITPayroll - Validation Professional Location: 126 E. Lincoln Avenue Rahway, NJ Qualifications: Education: Bachelors Degree with a minimum of 8+yrs of applicable experience Required: Knowledge of ADP Technology ev6, Workday, MS Office Candidate would need to be subject matter expert (SME) in ADP functi
$40,000 – $63,000/year
Estimation confidence: Low
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