At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
Skills: CSV, LABWARE LIMS, VALIDATE SYSTEM, 21 CFR PART 11, GAMP, Validation documentation & compliance, Were Hiring: CSV Engineer (LIMS Required for Select Locations) Experience: 1-5 Years Role Overview We are looking for CSV Engineers with experience in
Were Hiring CSV Engineer Location: Nagpur & Pune, Goa, Baddi, Dewas, Hyderabad(Vizag) Experience: 35 Years Department: Computer System Validation (CSV) Required Skills: LIMS Validation CSV Documentation LabSolution Software Validation IQ, OQ, PQ Execution Manufacturing System Validation Good knowledge of validation protocols & compliance
Skills: GxP Compliance, 21 CFR Part 11, Risk Assessment, Validation Protocols, Computerized System Validation (CSV), Validation, GAMP, Were Hiring! CSV Validation Engineer - Mandideep/Goa/Baddi /Nashik/Nagpur/Digwal(Hyderabad )/Dabasa/ Vizag /Indore Pan India Position: CSV Validation Engineer Company: INSTRUMENTATION AND CONTROL SOLUTIONS (ICS) Location: Mandideep/Goa/Baddi /Nashik/Nagpur/Digwal(Hyderabad
About the Job About Aligned Automation At Aligned Automation, we live by our Better Together philosophy to build a better world. As a strategic service provider to Fortune 500 companies, we help digitize enterprise operations and
OVERVIEW The Computer Systems Validation (CSV) Specialist, Trial Interactive reports to TransPerfect’s Director, QA & systems Validation, Trial Interactive and impacts all aspects of TransPerfect’s Life Sciences 21 CFR Part 11 and GCP/ICH compliance, as well as the latest ISO
OVERVIEW The Senior Computer Systems Validation (CSV) Associate, Trial Interactive, is responsible for supporting TransPerfects Life Sciences 21 CFR Part 11 and GCP/ICH compliance and helping to maintain the certified ISO 9001 Quality Management systems across all computerized systems. This role
OVERVIEW The Senior Computer Systems Validation (CSV) Associate, Trial Interactive, is responsible for supporting TransPerfects Life Sciences 21 CFR Part 11 and GCP/ICH compliance and helping to maintain the certified ISO 9001 Quality Management systems across all computerized systems. This role
OVERVIEW The Computer Systems Validation (CSV) Specialist, Trial Interactive reports to TransPerfect’s Director, QA & systems Validation, Trial Interactive and impacts all aspects of TransPerfect’s Life Sciences 21 CFR Part 11 and GCP/ICH compliance, as well as the latest ISO
Job Description Validation Lead – Computer System Validation (CSV) A Validation Lead in the Computer System Validation (CSV) domain is responsible for validating Gx P and Non-Gx P computerized systems in compliance with regulatory standards such as GAMP 5, FDA 21 CFR Part 11,
Experience:2-5 years Contract Role:6 Months The Computerized Quality Assurance (CQA) Validation Specialist is responsible for ensuring that computerized systems used in API manufacturing facilities comply with applicable regulatory requirements and internal quality standards. Knowledge on how to conduct validation of systems used
JOB DESCRIPTION (JD) Job Title: IT Executive / IT Officer Department: Information Technology Location: Kurkumbh Industry: API Pharmaceutical Manufacturing Reporting To: Plant Head / QA Head 1. Job Purpose: To manage and maintain IT infrastructure and
Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable
Additional Important Note For Applicants Currently, only immediate joiners (who have already completed their notice period) or candidates serving a notice period of up to 30 days will be considered for this opportunity. Candidates with longer
Job Description : Business: Piramal Critical Care Department: Quality eCompliance Location: Kurla Travel: Low Job Overview To ensure regulatory compliance of IT and electronic systems for Piramal critical care sites and corporate. Responsible to support in implementation
We are looking for a Senior ETL Test Engineer to join a global healthcare project focused on building a centralized repository for clinical trial data. The platform integrates data from multiple source systems and applies complex business
Job Description The Associate Director, Supplier Quality Management (SQM) will be responsible for all quality aspects related to external suppliers, contract manufacturers, and service providers supporting GMP operations. This role ensures compliance with company policies, procedures,
Description Tech Compliance Analyst I Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them
Title: Executive - QA Custom Field 2: 2867 Location: NEOU-1300, Gujarat, IN Country/Region: IN State: Guja City: NEOU-1300 Company: Dishman Carbogen Amcis Limited Business Unit: General Travel Description: Computerized Systems Lifecycle Management (CSV). Prime responsibility for Information Technology
Be the First to Apply Job Description Manager - Quality eComplianceJob Description Business: PPL Department: Quality eComplaince Location: Navi Mumbai Travel: Low Job Overview We are looking for a responsible professional to manage Computer System Validation (CSV) and