Quality Validation Officer

Responsibilities: Provide Quality oversight to equipment/system qualification, automation qualification (PCS/BAS) and cleaning validation Review and approve validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines timely Review and approve as needed, qualification/validation executed...

**Validation and Quality Assurance (VQA Engineer)Responsibilities: Conduct technical assessments for new suppliers and periodic assessments for key existing suppliers. Jointly develop supplier technical roadmap with supplier chain management. Communicate with suppliers regularly to develop quality improvement plans and foster an environment that facilitates...

Responsibilities: Initiate validation and qualification activities on new supplier, parts, processes and products as requested by related department to ensure compliance to QMS and business continuity. Provide support to the revalidation and requalification activities of Engineering according to the Validation Master Plan to ensure compliance to QMS. Create...

Roles & ResponsibilitiesMain Responsibilities：1. Assist Quality and Validation Manager Asia to complete the tasks in time with good quality.2. Responsible for successful execution the Validation functions for customer project, as required – Quality, Cost, Time.3. Responsible to drive and support project team for projects where validation is required and...

Roles & ResponsibilitiesMain Responsibilities：1. Assist Quality and Validation Manager Asia to complete the tasks in time with good quality.2. Responsible for successful execution the Validation functions for customer project, as required – Quality, Cost, Time.3. Responsible to drive and support project team for projects where validation is required and...

Roles & ResponsibilitiesThe OpportunityEsco Lifesciences Group, is Singapore’s most globalized life sciences company, with annual revenues close to SGD 200M and global operations in over 20 countries across North America, Europe and Asia.Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first introduced in 2017.At Esco Aster Pte Ltd, we...

Roles & ResponsibilitiesThe OpportunityEsco Lifesciences Group, is Singapore’s most globalized life sciences company, with annual revenues close to SGD 200M and global operations in over 20 countries across North America, Europe and Asia.Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first introduced in 2017.At Esco Aster Pte Ltd, we...

Roles & ResponsibilitiesResponsibilities: Responsible for monitoring and ensuring the quality of all the operation aspects of the facility according to the established SOP, GMP, GDP and GLP practices and regulatory requirements Responsible to brief the new operators on the GMP and hygiene briefing Responsible to brief the relevant maintenance, quality...

Perform risk-based commissioning, qualification and validation service for pharmaceutical and biopharmaceutical clients on one or more of the following areas:Process Equipment CIP / SIP Process Manufacturing and related business processes including Quality Operations and Supply Chain Operations Method validation (analytical chemistry, biochemistry,...

Up to $7000 with 2 months Variable Bonus, Permanent Position:- West Singapore:- Pharmaceutical Industry Experience is a MUST:Experiences in multiple CQV discipline (such as CIP, SIP)Responsibilities: Perform riskbased commissioning, qualification and validation service for pharmaceutical and biopharmaceutical clients on one or more of the following...

Roles & ResponsibilitiesMission DescriptionSupporting with execution of validation strategy during and leading up to shut down period (november'24 to Jan'25) in AMSProfile RequirementField experience with validation engineering Execution of validation, validation test, qualification test Have performed IQ and OQ and cleaning validation knowledge Worked with...

Roles & ResponsibilitiesMission DescriptionSupporting with execution of validation strategy during and leading up to shut down period (november'24 to Jan'25) in AMSProfile Requirement Field experience with validation engineering Execution of validation, validation test, qualification test Have performed IQ and OQ and cleaning validation knowledge Worked...

Roles & ResponsibilitiesPurpose: Support equipment qualification, system qualification, and cleaning validation.Responsibilities: Develop, review and/or approve validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines, and completed in a timely fashion. Lead project validation...

Roles & ResponsibilitiesPurpose: Support equipment qualification, system qualification, and cleaning validation.Responsibilities: Develop, review and/or approve validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines, and completed in a timely fashion. Lead project validation...

PES 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 multinational clients.We...

PES 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 multinational...

**MAIN PURPOSE To optimize existing processes (ie. yield, quality, efficiency) and to ensure that production goals are met. Maintain level of production and activities on an hourly, daily and monthly basis with strong engagement at shopfloor. Develop key leading indicator metric and monitor performance of equipment, machines and tools, timely correcting...

Job descriptionAbout the jobSupports Validation activities related to validation of facility, equipment and utilities.Support day-to-day Validation activities in accordance with approved Validation SOPs/Plan/Policies.Develop & execute Validation Protocols and Reports, including supporting site discrepancies and deviations investigation/closure.Collaborate...

No 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 strongly uphold our core...

Support equipment, facilities, utilities qualifications Develop validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines, and complete execution in a timely fashion Manage qualification execution and lead qualification deviation investigations encountered during qualification Collaborate...