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.
...To support a diverse network of business owners, the remote Brand and Web Designer will create cohesive brand identities and user-friendly websites while collaborating with clients and managing multiple projects on a contract basis.Key responsibilitiesDevelop and design...
...proven track record in EPC Industry working on projects involving pipelines, terminals, compressor stations, and fractionation facilities.... ...DUTIES:Lead projects involving transportation and storage of oil, gas, and petroleum products.Direct terminal facility design,...
...very best in post - acute rehabilitation services! Ft Washington has earned a reputation for providing excellent and compassionate nursing care. We are seeking motivated and compassionate RN'S to join our team! The RN promotes and restores residents' health by completing...
Hardware Systems Engineer, MidThe Opportunity:Are you looking for an opportunity to combine your technical skills with big picture thinking... ...vibration qualificationMaster's degree in Electrical Engineering, Computer Engineering, or related disciplineClearance:Applicants...
...Job Description Job Description Agency CNA $24 to $25/hr (Weekly Pay) Location: Brooklyn, NY 11218 (Nursing Home facility) Weekday Pay: $24 / hour Weekend Differential: $25 / hour Overtime Pay: $36 to $37.50 / hour Schedule: 7AM-3PM (Day), 3PM...