CSV validation Engineer

Role: Senior CSV ValidatorAbout Resource Informatics GroupWe are a leading provider of data validation services, specializing in CSV validation and assurance. Our team of experts is dedicated to delivering high-quality results, on-time and within budget.Key Responsibilities:Validate large CSV files to ensure data consistency and accuracyDevelop and implement...

We are seeking a highly skilled Computer System Validation (CSV) Engineer to join our client on a contract basis. This role is crucial for ensuring the validation and compliance of computerized systems in a regulated, GxP-compliant environment, contributing to the production of innovative oncology treatments. Key Responsibilities:Lead and Execute CSV...

Piper Companies is currently seeking an experienced Validation Engineer (CSV/CQV) in Raritan, NJ to work for an industry leading Pharmaceutical company. Responsibilities for the Validation Engineer (CSV/CQV) Provide technical expertise for commissioning, qualification, validation maintenance, and cleaning/sterilization processes while ensuring compliance...

Company DescriptionSince 1995, Supremesoft Corporation has been partnering with clients to strengthen their key business processes by identifying critical issues and implementing innovative customized solutions. Through the years, Supremesoft has grown steadily into a global information technology consulting company, by establishing and building a solid...

CQV engineer :Design Documentation: URS, FRS, DS, and other engineering specifications Validation Processes: IQ, OQ, PQ, Process Validation (PV), Computer Systems Validation (CSV), Master Validation Plan (MVP) Quality Systems: Change Control, Non-Conformances, Requalification protocols (IQ/OQ/PQ) in compliance with GMP, FDA, and other regulatory requirements...

Role: CSV Assurance ExpertAbout Resource Informatics GroupWe are a trusted provider of data validation services, specializing in CSV assurance and validation. Our team of experts is dedicated to delivering high-quality results, on-time and within budget.Key Responsibilities:Validate large CSV files to ensure data consistency and accuracyDevelop and implement...

CSV, Compliance and Assurance services, LIFE-SCIENCES (GXP FDA CSV IQ/OQ/PQ), Veeva, Argus, Defect Tracking Tools JIRA 10+ years' Experience in Validating systems and Experienced in CSV activities in GxP related applications like SAP Systems, Product Serialization systems, MES systems. Perform review for GxP systems to ensure compliance with regulatory...

Roles & Responsibilities:10+ years' Experience in Validating systems and Experienced in CSV activities in GxP related applications like SAP Systems, Product Serialization systems, MES systems. Perform review for GxP systems to ensure compliance with regulatory requirements Working knowledge on end-to-end validation of GxP applications and is able to perform...

Job Description Job Description Roles & Responsibilities:10+ years' Experience in Validating systems and Experienced in CSV activities in GxP related applications like SAP Systems, Product Serialization systems, MES systems.Perform review for GxP systems to ensure compliance with regulatory requirements Working knowledge on end-to-end validation of GxP...

Roles & Responsibilities: 10+ years' Experience in Validating systems and Experienced in CSV activities in GxP related applications like SAP Systems, Product Serialization systems, MES systems. Perform review for GxP systems to ensure compliance with regulatory requirements Working knowledge on end-to-end validation of GxP applications and is able to...

Job DescriptionAs a Validation Engineer (CSV/CQV), you will conduct IQ, OQ, and PQ activities, validate new laboratory equipment and methods, support software updates, and assist in creating SOPs, safety protocols, and work instructions. You will also oversee site validation master plans, ensure equipment and systems meet regulatory requirements, and...

About the RoleThis is an exciting opportunity to join a leading pharmaceutical company as a Validation Engineer (CSV/CQV). The selected candidate will have the chance to work on complex projects, develop their skills, and contribute to the company's growth and success. We are looking for a motivated and detail-oriented individual who can thrive in a...

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Roles & Responsibilities:Develop and execute comprehensive validation plans for packaging lines, labelers, case packers, and low-speed pen assembly systems.Lead the validation of SEA Vision Yudoo and AVI systems, ensuring strict compliance with industry standards and regulatory requirements.Author, execute, and document Installation Qualification (IQ),...

Job Title: Equipment Validation EngineerLocation: Jersey city, NJJob Description:We are seeking an experienced Equipment Validation Engineer for a long-term project with a leading pharmaceutical/biotech client. The ideal candidate will have a strong background in equipment validation within regulated environments and be capable of independently developing...

Title: Project EngineerLocation: NJResponsibilities: Prepare and execute cleaning, process and packaging validation, and equipment qualification plans and protocols. Write Final summary Reports that summarize executed qualifications/validations. Assist in the development, coordination, and execution of qualifications/validation protocols for systems governed...

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ResponsibilitiesResponsible for validation programs in support of GMP manufacturingResponsible for facility, utility and equipment qualification programsResponsible for QA role in process and assay validation programsReview or author validation related documents such as design specification, URS, FAT, SAT, IQ, OQ, PQ for utility and equipmentAssume QA lead...