CQ Manager, QC Lab — Lead GMP Validation

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...

About No deviationAt 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...

About No deviationAt 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...

A pharmaceutical consultancy in Singapore is seeking a highly skilled CQ Manager to lead the commissioning of Drug Substance manufacturing. Candidates should have over 10 years of CQV experience in biologics, with a strong understanding of GMP standards and bioprocess equipment. This role involves ensuring regulatory compliance and operational excellence in...

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...

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...

**Responsibilities**: - Qualify and validate laboratory equipment, including temperature control units. - Create new User Requirements Specifications (URS) for lab equipment. - Draft and execute validation protocols. - Troubleshoot and resolve validation issues. - Ensure compliance with regulatory standards and accurate documentation. - Collaborate with...

**Responsibilities: - Support the Quality Control Laboratories with independent, effective and timely testing services and able to ensure that tasks are performed according to requirements with review/verification of results and problem solving for issues identified. - Responsible for the timely completion and data verification of all testing of raw...

A leading recruitment agency is seeking a QC Expert for lab validation in Singapore. This role requires a university degree and 5 years of quality control experience in the pharmaceutical industry, focusing on compliance with regulatory standards. Responsibilities include maintaining validation plans, supporting inspections, and ensuring adherence to cGMP....

**QC Lab Technician** MiRXES is a Singapore-headquartered molecular diagnostic company with R&D, manufacturing, and clinical lab operations in Singapore, USA, Japan, and China. We specialize in microRNA technologies and the development, manufacturing, and provision of diagnostic test kits and clinical services. Our mission is to enable early disease...