74 csv opportunities in Raritan updated today
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· Page 1 / 4Job Description: Job Summary: CSV Consultant role supporting system validation activities in a regulated environment, ensuring compliance with FDA guidelines, GxP standards, and risk-based validation approaches. The role involves working within the System Development Lifecycle (SDLC) and contributin
Greetings from Inherent Technologies ! Hope this email finds you in the best of your health, My name is Bhanu, and I'm an IT recruiter at Inherent Technologies . Position: CSV Consultant Location: Raritan, NJ(Hybrid) Duration: 1 Year Job Details Ex-J&J preferred Experience in the Pharmaceutical,
Role - CSV Consultant Location - Raritan, NJ(Hybrid) Job Details: Experience in the Pharmaceutical, biotechnology, or medical device industry 2+ years experience with System Development Lifecyle 3+ years experience in Computer System Validation (Based on the role selected) Experience in FDA and/or G
Dice is the leading career destination for tech experts at every stage of their careers. Our client, Sharpedge Solutions, is seeking the following. Apply via Dice today! **Job Details: Ex-J&J preferred** Experience in the Pharmaceutical, biotechnology, or medical device industry 2+ years experie
Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakt
Ex-J&J preferred Experience in the Pharmaceutical, biotechnology, or medical device industry 2 years’ experience with System Development Lifecyle 3 years’ experience in Computer System Validation (Based on the role selected) Experience in FDA and/or Global regulated environment with good underst
Job Summary This mission-critical role leads the end-to-end implementation and validation of the Thermo SampleManager LIMS to support high-stakes laboratory operations. By bridging the gap between physical laboratory workflows and digital architecture, the Lead ensures the integrity of data supporti
Cognizant is always looking for top talent. We are searching for candidates to fill future needs within the business. This job posting represents potential future employment opportunities with Cognizant. Although the position is not currently available, we want to provide you with the opportunity to
CSV LIMS Lead Duties: Lead end-to-end implementation, configuration, and integration of Thermo Fisher SampleManager LIMS Gather existing laboratory and shop-floor workflows; translate them into digital processes Coordinate interfaces between LIMS and laboratory systems. Drive CSV activities: author
Lead end-to-end implementation, configuration, and integration of Thermo Fisher SampleManager LIMS Gather existing laboratory and shop-floor workflows; translate them into digital processes Coordinate interfaces between LIMS and laboratory systems. Drive CSV activities: author URS, execute IQ/OQ/PQ
A company is looking for a Sr. CSV Engineer / Sr. Validation Engineer. Key Responsibilities Lead development of the validation strategy within the first 30 days of onboarding Oversee CSA/CSV compliance execution aligned with customer SDLC and quality procedures Provide governance, review, and approv
*Role: CSV - Validation Lead** *Location: Raritan, NJ** *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| reviewing| revising| and maint
A pharmaceutical company is seeking a Quality/Validation Engineer with hands-on expertise in GxP-regulated environments and Computer System Validation (CSV). This role involves full lifecycle validation of systems like ERP and R&D platforms. The ideal candidate should have 8–10 years of experience,
Job Title: CSV Specialist Location: 113 14 Schoolhouse Road 13-4268760 Somerset N States Duration: 17+ Months (With possible extension) Education or Equivalent: Bachelor of Science in an Engineering, Computer Systems or Science Field. Specific Duties, Activities, and Responsibilities: • Hands-on CSV
A pharmaceutical company is seeking a Quality/Validation Engineer with hands-on expertise in GxP-regulated environments and Computer System Validation (CSV). This role involves full lifecycle validation of systems like ERP and R&D platforms. The ideal candidate should have 8–10 years of experience,
Roles and Responsibilities: Lead end-to-end Computer System Validation for GxP systems. Develop and review URS, risk assessments, IQ/OQ/PQ protocols, and validation reports. Ensure compliance with FDA 21 CFR Part 11, GAMP 5, and GxP. Manage validation risk and maintain systems in a validated state.
Katalyst HealthCares & Life SciencesJob Posting Analyze and evaluate current business processes, anticipate future requirements, identify areas for improvement, and develop and implement effective solutions. Utilize both formal and informal communication methods to stay updated on customer needs and strategies. Communicate updates and
Legend 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
Creates Computer System Validation (CSV) deliverables (Validation Plan, Requirements Specifications, Protocols, Summary Reports, Trace Matrices, SOPs, Risk assessments). Collaborates with Business Users, System Owner, Global IT teams and Business Analysts to define validation requirements and plans.
ConfidentialRole: CSV - Validation Lead Location: Raritan, NJ 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| reviewing| revising| and maintaining valid
Responsibilities: Creates Computer System Validation (CSV) deliverables (Validation Plan, Requirements Specifications, Protocols, Summary Reports, Trace Matrices, SOPs, Risk assessments). Collaborates with Business Users, System Owner, Global IT teams and Business Analysts to define validation requi
Insmed IncorporatedAt Insmed, every moment and every patient counts — and so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you’ll be part of a community that prioritizes the human experience, celebrates curiosity, a
Project Module Work Plans To create, assign, and track the project module work plans for delivery and also provide technical guidance for work completion. To ensure process improvement and compliance in the assigned module, and participate in technical discussions/review. To create work plans, monit
Job Description: * Responsible for preparing and executing test documentation for GMP computerized systems as well as providing support in the troubleshooting of issues during test execution. * You should have excellent understanding of 21 CFR Part 11, ICH standards, EMA and FDA (GxP) regulations, a
To create| assign and track the project [module] work plans for delivery and also provide technical guidance for work completion. (1.) To ensure process improvement and compliance in the assigned module| and participate in technical discussions/review. (2.) To create work plans| monitor and track th
Job Description: • Analyze and evaluate current business processes, anticipate future requirements, identify areas for improvement, and develop and implement effective solutions. • Utilize both formal and informal communication methods to stay updated on customer needs and strategies. Communicate up
IT CSV Engineer (Hybrid) Location: Somerset,NJ Interview:Phone+Skype most important skillset is experience with Snowflake and AI. The IT CSV Validation Engineer is responsible for authoring and executing validation test scripts to support regulated systems within a GxP life sciences environment. Thi
Responsible for managing end-to-end CSV deliverables for both new & existing applications. Responsible for Implementation of Lab, Enterprise and Manufacturing systems and supporting change management of existing systems. Manage and support CSV Consultants on execution responsibilities & be direct in
Acadia Pharmaceuticals Inc.*About Acadia Pharmaceuticals** Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinso
$40,000 – $63,000/year
Estimation confidence: Low
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