CQ Manager Drug Substance: Lead Bioprocess Validation

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 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...

**OBJECTIVES**: Responsible for planning and supporting the Dengue Drug Substance Process Technology Transfer from Takeda to Contract Manufacturing Organization (CMO) in India. Includes document/knowledge transfer activities, process design and improvements, process scale-up, GMP Production, and validation aspect of the manufacturing. Involved in developing...

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...

A leading pharmaceutical consultancy in Singapore is seeking a CQ Manager QC Laboratory to lead the commissioning and qualification of analytical laboratories. You will collaborate with cross-functional teams to ensure compliance with GMP standards while overseeing the installation and validation of laboratory systems. The ideal candidate has over 10 years...

A leading biopharmaceutical company in Singapore is seeking experienced professionals to perform bioconjugation reactions and purification of drug substances. The ideal candidate will have a diploma or degree in a relevant field with 3-5 years of experience, along with strong communication and methodical work habits. This role requires adaptability to a GMP...

A leading biopharmaceutical firm in Singapore is seeking a candidate for bioconjugation reactions and purification of antibody intermediates. The ideal applicant has a Diploma or Degree in a relevant field, with 3-5 years of experience. Responsibilities include ensuring compliance with quality standards in drug substance manufacturing operations. Candidates...

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...

Subject Matter Expert in cleaning validation and SIP validation lifecycle, from design requirement analysis to retirement for drug substance and drug product manufacturing. Job Responsibilities Role & Responsibilities General: Serve as SME for Cleaning Validation and SIP Validation for the Singapore facilities for Drug Product and Drug Substance Ensure...