Job-ID33104459Reference26-01807Job Summary: We are seeking a motivated and detail-oriented Computer System Validation (CSV) Engineer with 1–2 years of experience to support validation and compliance activities within the Pharmaceutical and Medical Devic e industries. The ideal candidate will assist with the validation of computerized systems in regulated GxP environments and ensure systems comply with applicable regulatory and quality requirements. The candidate should have a strong understanding of validation principles, documentation practices, data integrity, and regulatory expectations. Roles and Responsibilities:Support the planning, execution, and documentation of Computer System Validation (CSV) activities for GxP-regulated computerized systems. Support system impact assessments, risk assessments, and validation strategy development. Execute or assist with validation test scripts and document test results, deviations, and observations. Ensure validation deliverables comply with applicable FDA regulations, GxP requirements, 21 CFR Part 11, and Data Integrity principles. Assist with reviewing computerized systems for compliance with electronic records and electronic signatures requirements. Support deviation, change control, CAPA, and validation lifecycle activities as required. Collaborate with Quality Assurance, IT, Engineering, Manufacturing, and other cross-functional teams. Maintain accurate and complete validation records in accordance with company procedures and regulatory requirements. Participate in internal and external audits by providing appropriate validation documentation and support. Identify potential compliance gaps and assist in developing appropriate remediation activities. Stay current with relevant regulatory requirements, industry standards, and CSV best practices. Education & Experience: Bachelor's degree in engineering, Computer Science, Information Systems, Life Sciences, Pharmaceutical Sciences, or a related technical field. Relevant coursework or training in Computer System Validation, GxP, Quality Assurance, Regulatory Compliance, or Software Quality is a plus.1–2 years of professional experience in Computer System Validation (CSV), Validation, Quality Assurance, Compliance, or a related regulated industry. Experience supporting validation activities within the Pharmaceutical, Biotechnology, Medical Device, or other FDA-regulated industries is preferred.
...Benefits: Flexible schedule Free uniforms Training & development JOIN THE SHOW YOU HAWAII OHANA! Now Hiring Part-Time Tour Guides & Drivers Love meeting new people? Enjoy driving and sharing the beauty of Hawaii Island? Turn your passion for Hawaii into...
...deserves compassionate, dignified care that enhances quality of life... ...to them. As a member of our Palliative Care team in Billings,... ...with an Expert Team including physicians, advanced practice providers,... ...workers, chaplains, therapists, hospice teams, and other specialists....
...Job Description Job Description Hertz is hiring an experienced Diesel Bus Mechanic to join our team. If you have strong bus maintenance experience, enjoy hands-on troubleshooting, and want to work for an established industry leader, this is a great opportunity to...
...Trauma Program contract. Position Summary The Community Mental Health Worker (CMHW) is responsible for providing trauma-informed,... ...Work Psychology Human Services Sociology Counseling Public Health Family Studies Criminal Justice Related...
...expertise. Here, you can apply your passion and collaborate with top environmental professionals on work thats vital to our clients and the... ....Stantec is seeking a dynamic and results-driven Senior Consultant to lead business growth and project delivery across the New England...