Job-ID32575457Reference26-01231Remote50% Remote Job Description: We are seeking a Computer System Validation (CSV) Engineer for a global pharmaceutical client. This role will work cross-functionally to lead and execute validation activities for GxP electronic systems and applications. The CSV Engineer will partner with Business Owners, Technical Owners, and Quality teams to create and manage validation deliverables throughout the validation lifecycle. The primary responsibility is to ensure that validation activities supporting Manufacturing Execution Systems (MES) are documented in accordance with applicable procedures and regulatory requirements. Roles & Responsibilities: Author, review, and/or approve applicable CSV documentation. Assist Business Owners and Technical Owners during test execution, document test failures, and ensure testing aligns with internal procedures. Assist Business Owners and Technical Owners in developing requirements and specifications for computerized systems used in GxP operations. Support validation activities for Manufacturing Execution Systems (MES). Develop and maintain CSV documentation including Validation Plans, Requirements, Specifications, Assessments, Test Scripts (IQ/OQ/PQ or equivalent), Summary Reports, Trace Matrices, and SOPs. Ensure compliance with cGMP, GxP, GAMP, SDLC regulations, 21 CFR Part 11, and Good Documentation Practices. Support validation of pharmaceutical manufacturing and laboratory systems used in biologics and clinical manufacturing environments. Utilize IT service management platforms to support incident, problem, and change management activities. Work with Business Quality Management Systems and related validation processes. Requirements: Bachelor's degree in Life Sciences, Engineering, IT, or a related discipline, or equivalent industry experience. Minimum 4+ years of direct experience in Computer System Validation (CSV). Strong knowledge of GAMP and risk-based validation approaches. Good understanding of electronic records and electronic signatures. Strong knowledge of Manufacturing Execution System (MES) validation. Familiarity with MES systems such as Emerson Syncade, ERP systems such as SAP or Oracle, and EBR systems such as InfoBatch. Strong experience developing CSV documentation, including Validation Plans, Requirements, Specifications, Assessments, Test Scripts, Summary Reports, Trace Matrices, and SOPs. Knowledge of pharmaceutical, manufacturing, and laboratory systems supporting biologics and clinical manufacturing. Experience with IT service management platforms such as ServiceNow. Exposure to Business Quality Management Systems such as Veeva.
...Job Description Job Description Partime Mail carrier to work 1 week on 1 week off, must have a dependable SUV. Must report to work on time, Must have some experience in delivering mail or packages. Must be dependable and must effectively communiciate. The pay is to...
St. Lukes Health System in Idaho seeks a Medical Interpreter/Translator to provide accurate interpretation for patients and staff across clinical and general settings.You will interpret complex medical information, assess patient understanding, and advise on cultural...
...At PwC, our people in tax services focus on providing advice and guidance to clients on tax planning, compliance, and strategy. These individuals help businesses navigate complex tax regulations and optimise their tax positions. In indirect tax at PwC, you will focus...
...Gold Seal Quality Program and nationally accredited early childhood center we believe the most powerful learning happens before kindergarten. We are looking for a passionate Preschool Teacher who finds joy in a child's curiosity, leads with patience and creativity, and...
...Tower Construction Crew ChiefTower Crew Chief must be able to adhere to rigid safety standards while ensuring quality work in a fast-paced... ...situations.Compensation: $25-$33 based on experience. Weekly per diem checks issued where room and board is applicable. Tower Techs...