Qc Csv Engineer

We are seeking a Computer System Validation (CSV) Engineer with around 5 years of relevant experience to support QC and laboratory operations in a regulated GMP environment. The role involves ensuring that computerized systems and laboratory equipment are validated, maintained, and compliant with regulatory standards, while supporting continuous improvement...

**Role Overview** We are seeking a QC Engineer with strong experience in **Computer System Validation (CSV)** for analytical laboratory instruments /equipment. The role ensures compliance with 21 CFR Part 11, data integrity, and global validation standards in a regulated GMP environment. **Key Responsibilities** - Lead CSV activities for **analytical...

Job Title and Industry Job Title: Benchtop IT / CSV Engineer – QC Laboratory Systems Industry: Life Sciences / Pharmaceutical Manufacturing Role Overview We are seeking a Benchtop IT / CSV Engineer to support validation and compliance activities for laboratory computerized systems and instruments used in QC and analytical environments. The role involves...

We are looking for a QC Engineer to support **validation of analytical laboratory instruments and computerized systems**in a GMP-regulated environment. The role focuses on ensuring compliance with 21 CFR Part 11, Annex 11, ALCOA+ principles, and data integrity requirements. **Key Responsibilities**: - Plan, execute, and document qualification/validation of...

Overview We are seeking a skilled CSV Engineer to provide quality oversight and validation support across the computerized system lifecycle within a biologics manufacturing environment. This role requires deep understanding of GxP standards, data integrity, and regulatory compliance, with hands-on experience in validating complex automation and IT systems....

Role Overview:We are seeking a Junior CSV Engineer to join Anter to support Computer System Validation (CSV) activities for pharmaceutical clients in Singapore. The role involves assisting with validation execution, documentation, and compliance to ensure systems meet regulatory and quality standards.Key Responsibilities:Assist in the preparation, execution,...

**Senior CSV Engineer**: - Contract - Onsite - Singapore, Singapore - CQV - 7316 - SGD **Overview - We have an immediate requirement for 2 - **CSV Specialists **to join a highly skilled PM Group team based on a client site. **Responsibilities **Day to day activities include the following**_:_** - Commissioning and Qualification of hardware and associated...

Overview Join to apply for the CSV Engineer role at Antaes Asia . 4 days ago Be among the first 25 applicants. Responsibilities Contribute to Life Science projects for Antaes Asia clients. Work with cross-functional teams in providing Quality oversight in computerized system life cycle procedures and ensure compliance with GXP standards and company policies...

About No deviation At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful...

**Responsibilities**: - Lead and execute Computerized Systems Validation (CSV) activities, including planning, testing, documentation, and reporting. - Collaborate closely with the Compliance Engineering team to support commissioning, qualification, and validation (CQV) activities. - Prepare, review, and approve qualification documentation (URS, DQ, FAT,...