Job Title: CSV Engineer Location: Raritan, NJ - Onsite Duration: 6+ months Contract Job Description: 3-7 years... identified risks. Key Skills: CSV, Servicenow, JIRA, 21 CFR Part11, GxP, FDA, Quality Management, GAMP, Validation....
productivity, data integrity / compliance, quality, and operational excellence. Digital Manufacturing Technologies include digital... Engineer – Computer System Validation and Data Integrity is an Engineering role will be the corporate engineering Computer...
Role - CSV Engineer Location - Raritan, NJ (Hybrid 3 days onsite) Must Have: The resource must have experience... or Quality management or Business Analysis in GxP application area. Has working experience in any one or two of the following...
our collective expertise Senior CSV Engineer Responsibilities: We are seeking a skilled Computer System Validation (CSV.... Responsibilities Include: Develop and execute CSV protocols, including Installation Qualification (IQ), Operational Qualification (OQ...
, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers... the test cases reflect business rules and processes. Fulfills a subject matter expert role(s) for critical quality...
Responsibilities: Participate on teams of internal resources in delivery of CSV projects. Author functional..., laboratory systems, quality management systems, ERPs, clinical trial and pharmacovigilance applications. Experience...
, DS, and other engineering specifications), Validation (IQ, OQ, PQ, PV, CSV, MVP, etc.), Quality Systems (Change Control...Responsibilities: Draft and implement Quality System documentation designed to establish good validation practices...
, DS, and other engineering specifications), Validation (IQ, OQ, PQ, PV, CSV, MVP, etc.), Quality Systems (Change Control...Responsibilities: Draft and implement Quality System documentation designed to establish good validation practices...
Responsibilities: Develop and execute CSV protocols, including Installation Qualification (IQ), Operational... and generate compliance reports, managing deviations and ensuring all required documentation meets quality and regulatory standards...
Responsibilities: To ensure the quality of our client's software applications and equipment by validating/qualifying... for Engineer I's. Submit specification, protocol and reports for approvals and documentation control via a Change Request...
Role & Responsibilities: 3-7 years' experience in Computer System Validation or Quality management or Business...
with different SDLC processes and Tools. Requirements: 3-7 years' experience in Computer System Validation or Quality Management...
System Validation or Quality management or Business Analysis in GxP application area. Guide the project team with the right...
or Quality management or Business Analysis in GxP application area. Guide the project team with the right set of applicable...
to process control systems of pharmaceutical water for injection system, water pretreatment system, water stills and high-quality...
to process control systems of pharmaceutical water for injection system, water pretreatment system, water stills and high-quality...
to process control systems of pharmaceutical water for injection system, water pretreatment system, water stills and high-quality...
listed above. Certification/Licensure: Certifications like Certified Quality Auditor (CQA), Certified Quality Engineer (CQE... projects, ensuring timely delivery, meeting specifications, and maintaining quality throughout. Prepare clear and concise...
Title: Computer System Validation (CSV) Specialist Location: Nashville TN Duration: Full Time... validation documentation, managing deviations, ensuring regulatory compliance, and providing ongoing support for systems. A CSV...
Software Design Quality Assurance Engineer. You will interact with the NPD and Product Sustain teams to assure quality... and associated traces. Complete CSV/CSA on Quality System Tools Mentor engineering staff in planning software development tasks...