System Validation

Responsibilities: Create and refine validation protocols for GxP critical reports, focusing on Computerized Equipment Validation within the QC lab. Configure static Master Data for validated/GMPcompliant LabWare LIMS (version 6), specifically emphasizing Computerized Equipment. Actively participate in executing, reviewing, and approving validation protocols...

Roles & ResponsibilitiesWe are seeking an experienced Computer System Validation Consultant to help drive our solution-based business model and take our designs to the next level. Our consultants have the chance to work hands-on with several business divisions to design, develop, test industry-leading solutions for our clients—both nationally and...

Roles & ResponsibilitiesWe are seeking an experienced Computer System Validation Consultant to help drive our solution-based business model and take our designs to the next level. Our consultants have the chance to work hands-on with several business divisions to design, develop, test industry-leading solutions for our clients—both nationally and...

Roles & ResponsibilitiesPharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world...

Roles & ResponsibilitiesPharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world...

Roles & ResponsibilitiesResponsibilities- Consults with management, assesses customer requirements, and studies product characteristics to select validation objectives and standards.- Prepares protocols for validation or performance testing of new or modified manufacturing equipment, processes, or systems.- Analyzes data from validation tests to determine...

About the job Serve as a site Subject Matter Expert for at least 1 specialized validation area Planning, performance, support and coordination of Computer System Validation, Equipment validation, Sterilization In Place, cleanroom validation, Clean Utilities Validation (IQ/OQ/PQ/CPV) Maintain validation status of Computer System Validation Independently...

Roles & ResponsibilitiesResponsibilitiesConsults with management, assesses customer requirements, and studies product characteristics to select validation objectives and standards.Prepares protocols for validation or performance testing of new or modified manufacturing equipment, processes, or systems.Analyzes data from validation tests to determine whether...

Responsibilities: Support equipment/system qualification and cleaning validation Develop cleaning validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines, and completed in a timely fashion Manage qualification/validation execution and lead the validation deviation investigations...

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 & 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 & ResponsibilitiesValidation engineers manage, inspect, calibrate, test and modify the instrumentation, equipment, mechanics and procedures used in manufacturing. A critical aspect of their job is documenting this process so there is evidence that systems are operating safely and efficiently.Validation engineers can be found in a range of industries,...

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 & ResponsibilitiesJobscope:Ensure that the manufacturing facilities, process and systems are validated in full compliance with cGMP and regulatory requirements so as to meet the stipulated product quality standards in line with established specifications of the organization. Play a key role in assessing, reviewing and approving changes that may have an...

Roles & ResponsibilitiesThe Verification & Validation Engineer is responsible for: Verifying the impact of System Engineering Change Requests (ECR's) and defining and submitting on-time and on-budget, test procedures and associated scenarios to the System Engineering Manager or Project Managers, in order to verify and validate the system (off-line,...

Roles & ResponsibilitiesRoles & ResponsibilitiesThe Senior Computer System Validation (CSV) Engineer will be based in one of clients who is among the top tier pharmaceutical giants. The engineer will provide a wide range of support for GMP Computerized System and Data Integrity Activities at site.Responsibilities Coordinate/manage multiple small and large...

Job descriptionAbout the jobDevelop, review and/or approve validation lifecycle documents and protocols/reports in accordance with relevant policies, standards, procedures, and guidelines, and completed in a timely fashion.Lead project validation activities and provide basic guidance and direction to junior project engineers as required.Review Turnover /...