CQV Engineer

Roles & ResponsibilitiesAbout the RoleWe are seeking a CQV Engineer to support commissioning, qualification, and validation activities for a pharmaceutical manufacturing facility in Singapore. The role involves ensuring compliance with GMP standards and regulatory requirements while executing validation protocols.Key ResponsibilitiesDevelop and execute CQV...

Roles & ResponsibilitiesWe are seeking a skilled CQV Engineer to support commissioning, qualification, and validation activities for a pharmaceutical company in Singapore. The ideal candidate will have experience in CQV processes for equipment, facilities, and utilities within a regulated environment. This role requires strong technical expertise, regulatory...

Roles & ResponsibilitiesAbout 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...

Roles & ResponsibilitiesWe are seeking highly skilled Commissioning, Qualification, and Validation (CQV) Engineers to provide risk-based CQV services for pharmaceutical and biopharmaceutical clients. This role offers opportunities to work across various areas, including process equipment, CIP/SIP (Clean-In-Place/Sterilize-In-Place), and process manufacturing...

Roles & ResponsibilitiesWe are seeking highly skilled Commissioning, Qualification, and Validation (CQV) Engineers to provide risk-based CQV services for pharmaceutical and biopharmaceutical clients. This role offers opportunities to work across various areas, including process equipment, CIP/SIP (Clean-In-Place/Sterilize-In-Place), and process manufacturing...

Provide effective leadership, coaching and conflict resolution to the project team in order to meet project goals and objectivesIndependently capable of doing process flow diagram, batch size calculation, process balance, equipment sizing, working area calculation, risk analysis, FMEA, VMP, CQV, QMS, etc.Independently capable of preparing URS for process...

Roles & ResponsibilitiesPES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.With offices across Europe, Asia and US, our core focus is on consistently delivering high-quality outcomes for our...

Roles & ResponsibilitiesSenior Consultant – Thermal MappingResponsibilities:Lead on-site test execution, guiding and overseeing junior consultants. Execute qualification protocols per GMP and ALCOA++ standards, including:Installation verification (voltage check, drawings/user manual verification).Operational verification (alarm verification, empty-load...

Roles & ResponsibilitiesSenior Consultant – Thermal MappingResponsibilities: Lead on-site test execution, guiding and overseeing junior consultants. Execute qualification protocols per GMP and ALCOA++ standards, including:Installation verification (voltage check, drawings/user manual verification).Operational verification (alarm verification, empty-load...

Roles & ResponsibilitiesPES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.With offices across Europe, Asia and US, our core focus is on consistently delivering high quality outcomes for our...

Roles & ResponsibilitiesPES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.With offices across Europe, Asia and US, our core focus is on consistently delivering high quality outcomes for our...

Roles & ResponsibilitiesSenior Consultant – Document ControllerResponsibilities:Ensure documentation compliance with Data Integrity and ALCOA++ principles. Review and complete qualification protocols for pharmaceutical systems (e.g., CTUs, BSCs, Autoclaves). Mentor and oversee junior consultants in documentation and protocol reviews. Apply knowledge of...

Roles & ResponsibilitiesNo Deviation is a provider of patient-centric solutions for the pharmaceutical industry, and we are currently seeking individuals who are passionate about joining our team.Our areas of expertise include engineering consultancy, Commissioning Qualification Validation (CQV), as well as Quality, Compliance, and Regulatory services.We...

Roles & ResponsibilitiesPES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.With offices across Europe, Asia and US, our core focus is on consistently delivering high quality outcomes for our...

Roles & ResponsibilitiesSenior Consultant – Document ControllerResponsibilities: Ensure documentation compliance with Data Integrity and ALCOA++ principles. Review and complete qualification protocols for pharmaceutical systems (e.g., CTUs, BSCs, Autoclaves). Mentor and oversee junior consultants in documentation and protocol reviews. Apply knowledge...

Roles & ResponsibilitiesPES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.With offices across Europe, Asia and US, our core focus is on consistently delivering high quality outcomes for our...

Roles & ResponsibilitiesNo Deviation is a provider of patient-centric solutions for the pharmaceutical industry, and we are currently seeking individuals who are passionate about joining our team.Our areas of expertise include engineering consultancy, Commissioning Qualification Validation (CQV), as well as Quality, Compliance, and Regulatory services.We...

Roles & ResponsibilitiesAbout 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...

Roles & ResponsibilitiesJob title: Process leaderReporting line:Direct Reports: Engineering DirectorJob overview:As the Process leader, Lead Singapore API engineering activities, ensuring cGMP compliance with Singapore HSA, FDA 21 CFR Part 211, and ICH Q7 requirements. Drive technical excellence in synthetic peptide & high-potency API manufacturing facility...