csv

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAs part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our...

Role TitleComputer System Validation (CSV) LeadLocationHybrid / Remote with occasional travel to manufacturing sites as requiredFlexibility to support global teams and multiple time zones is preferred.Role SummaryWe are seeking an experienced Computer System Validation (CSV) Lead to support a large-scale global life sciences manufacturing technology...

Job description Role & responsibilities At least 4-5 years of computer system validation experience in a Life sciences and pharmaceutical environment. Good knowledge of cGxP regulations and software lifecycle approaches (e.g., 21 CFR part 11, EU Annex 11, GAMP 5, SDLC Waterfall/Agile methodologies) Having good understanding on Computer system Assurance...

This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ business community. Please do not contact the recruiter directly. Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful...

Knowledge of IT Hardware/Network/Software Application componentsSound knowledge of Data backup technologies & SQL DatabaseSound knowledge of Audit trail review of instrument/Equipment/Computerized systemsPreparation & Perform validation documentation of PLC/SCADA, Computerized systemsSound knowledge of US FDA, 21 CFR Part 11, EU Annex 11 and GAMP5Sound...

  Job Title: Engineering CSV & QMS Manger Business Unit: Sun Global Operations Job Grade G10 Location: Dadra         At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive...

To ensure 21 CFR Part 11 Compliance in Manufacturing and QC of Troikaa Pharmaceuticals Ltd. To perform and evaluate the adequacy of Computerized System Validation across all sites of Troikaa Pharmaceuticals Ltd. To prepare, review and implementation of Corporate Policies and Standard Operating Procedures for Computerized Systems. To perform CSV compliance...

Summary RxLogix is an innovative company developing cutting edge software products for the pharmaceutical industry. We are seeking passionate candidates to join our QA team in Noida, India.  We offer competitive salaries, and other benefits to make sure everyone here has a stake in our success. We're a fast-growing organization looking for talented people...

Key Responsibilities: Computerized System Validation (CSV): Provide validation expertise on GxP-compliant applications in the drug safety space. Serve as SME in CSV practices , ensuring best practices are consistently followed. Review and approve key CSV deliverables: Requirement Specifications, Validation Plans, Test Plans, Traceability Matrix, Test...

Nomura Overview:   Nomura is a global financial services group with an integrated network spanning approximately 30 countries and regions. By connecting markets East & West, Nomura services the needs of individuals, institutions, corporates and governments through its three business divisions: Wealth Management, Investment   Management, and Wholesale...

Job descriptionAbout the Role:We are seeking a seasoned Computer System Validation (CSV) and Regulatory Compliance Specialist with a strong background in GxP, GAMP 5, and 21 CFR Part 11 to lead and support the validation of our technology platforms, applications, and services. This individual will work closely with cross-functional teams to ensure that all...

Qualifications & Skills Bachelor's or Master's degree in Computer Science, Life Sciences, Engineering, Pharmacy, or related field. 3–8+ years of experience in Computer System Validation within GxP-regulated industries (pharma, biotech, medical devices). Strong knowledge of GAMP 5 guidelines, FDA 21 CFR Part 11, EU Annex 11, and Data Integrity...

 HIRING: Computer System Validation (CSV) Specialist  Locations: Hyderabad | Bengaluru | Chennai | Pune Shift: 12 PM – 9 PM Experience: 4–8 Years CTC: ₹14–15 LPA Domain: CSV | GPV | GxP Role OverviewWe are looking for an experienced Computer System Validation (CSV) professional with strong exposure to GxP-regulated environments and validation...

Job descriptionOVERVIEW: The CSV (Computer Systems Validation) Manager, Trial Interactive leads and advances TransPerfect's global Life Sciences compliance initiatives, including 21 CFR Part 11, GCP/ICH requirements, and the company's ISO 9001-certified Quality Management System (QMS). The role holds direct accountability for the validation, governance, and...

Experience: 2 to 5 years(Only immediate joiners should apply) About The Job The CSV Engineer must be a self-starter, task oriented, maintain a strong work ethic, offer more than is asked for, and have the potential to see the big picture. Responsibilities • Developing Engineering documentation such as URS, Design Specifications (FS, HDS, and SDS,...

Job Title: Engineering CSV & QMS Manger Business Unit: Sun Global Operations Job Grade G10 Location: Dadra At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As...

  At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our...

About the JobAbout Aligned AutomationAt 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 drive impactful business strategies. Our purpose goes beyond projects—we strive to deliver meaningful, sustainable change that...

Job Description SummaryJob Description SummarySandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambitious path, unique opportunities will present themselves, both professionally and personally. Join us, the future is...

- 8+ years of experience in Computer System Validation (CSV) within the pharmaceutical or life sciences industry. - Strong knowledge of GxP regulations, FDA requirements, and industry compliance standards governing validated systems.- Proven experience in preparing, reviewing, and approving validation deliverables, including Validation Plans, Risk...