Validation Engineer #69403

Roles & ResponsibilitiesJob DescriptionIndustry/ Organization Type: Manufacturing Position Title: Validation Engineer Working Location: Tai Seng Working Hours: 5 days (Monday to Friday, 8.30 AM – 6 PM) Salary Package: Basic Salary up to $6,000 + AWS + Performance Bonus Duration: PermanentKey ResponsibilitiesAssist Quality and Validation Manager Asia...

Roles & ResponsibilitiesValidation / Calibration· Provides the subject-matter expertise to the site on Validation and Calibration.· Ensures all Validation related activities adhere to required policies and procedures.· Assists the site teams in preparation and execution of validation protocols.· As needed, liaises with Engineering and external vendors...

**Validation Engineer / Validation Manager**: At Genetic Design and Magic Corporation (GDMC), our mission is to exponentially increase the availability of genetic medicines and change millions of patients' lives. We achieve this by partnering and supporting early-stage companies and investigators with innovative therapeutic modalities such as gene therapies...

**Mission Description** Supporting with execution of validation strategy during and leading up to shut down period (november'24 to Jan'25) in AMS **Profile Requirement** - Field experience with validation engineering - Execution of validation, validation test, qualification test - Have performed IQ and OQ and cleaning validation knowledge - Worked with...

Roles & Responsibilities **Department**:MSAT **Reports to**:Validation Manager **Purpose** Support equipment qualification and cleaning validation. **Key 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...

**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 -...

**Job Description & Requirements**: - Completing work assignments as specified by the Validation Project Manager - Providing timely updates to the Validation Project Manager - Adhering to the proper site safety practices; wearing adequate safety equipment when required - Completing timesheets and expense reports in a timely manner - Working in a...

Roles & ResponsibilitiesProcess Engineer/ Validation Engineer/ Equipment / Molding / Medical / ManufacturingWorking Hours: 8.15 - 5.45pm Mon -Fri Permanent Position / MNC/ Urgent hiring Near Woodlands InterchangeOur client is a global advanced precision engineering & manufacturing solutions provider.Responsibilities:Prepare and execute process validation...

Roles & ResponsibilitiesProcess Engineer/ Validation Engineer/ Equipment / Molding / Medical / ManufacturingWorking Hours: 8.15 - 5.45pm Mon -Fri Permanent Position / MNC/ Urgent hiring Near Woodlands InterchangeOur client is a global advanced precision engineering & manufacturing solutions provider.Responsibilities:Prepare and execute process validation...

**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 -...

**Key Responsibilities**: - Assist the Quality and Validation Manager in completing validation tasks on time and with high quality. - Execute validation functions for customer projects, focusing on quality, cost, and time efficiency. - Collaborate with cross-functional teams to ensure all aspects of the validation process are addressed. - Conduct thorough...

This role is responsible for supporting validation activities including develop, support and implementation. In this role, the engineer must ensure qualification activities are performed in accordance with the company’s policies and procedures, and regulatory requirements **Responsibilities**: - Support equipment, facilities, utilities qualifications, -...

This role is responsible for supporting validation activities including develop, support and implementation. In this role, the engineer must ensure qualification activities are performed in accordance with the company’s policies and procedures, and regulatory requirements **Responsibilities**: - Support equipment, facilities, utilities qualifications, -...

This role is responsible for supporting validation activities including develop, support and implementation. In this role, the engineer must ensure qualification activities are performed in accordance with the company’s policies and procedures, and regulatory requirements **Responsibilities**: - Support equipment, facilities, utilities qualifications, -...

**Key responsibilities: - Perform Equipment Validation Maintenance Quality Systems review and re-qualification activities to ensure GMP equipment is continuously maintained in a validated state. Schedule own tasks to be performed as well as tasks for other Specialists as determined by the Validation Manager - Perform change control assessments for GMP...

Job description About the job Develop, 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 /...

**Who are we?**: **Amaris Consulting** is an independent technology consulting firm providing guidance and solutions to businesses. With more than 1000 clients across the globe, we have been rolling out solutions in major projects for over a decade - this is made possible by an international team of 6000 people spread across 5 continents and more than 60...

Responsibilities: - Responsible for executing and closing out the validation activities within the assigned area. - Develop or support the development of required validation documents, including Risk Assessments, plans, protocols, and reports. - Support the review, analyse, interpret and summarise data of executed studies. - Investigate or support the...

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 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 impactful...