System Validation Engineer

**Our vision is to transform how the world uses information to enrich life for all. **Join an inclusive team passionate about one thing: using their expertise in the relentless pursuit of innovation for customers and partners. The solutions we build help make everything from virtual reality experiences to breakthroughs in neural networks possible. We do it...

About the Role:We are looking for a skilled System Validation Engineer to join our team at Silicon Laboratories International Pte. Ltd. The successful candidate will have strong analog and digital circuit analysis skills, as well as experience in post-silicon validation.

Work closely with project team to assist Quality and Validation Manager Asia region to the tasks on schedule and within quality standard compliance. - Responsible completion of the Quality, Cost, and Time validation functions for customer projects. - Create and maintain qualification/validation documentation for mechanical, software, and hardware components...

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...

**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...

**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...

**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 -...

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...

**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 & 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...

As a CSV Engineer, you will be working for our clients in the respect of the applicable regulations and quality procedures. Main assignments: - To be responsible for preparing and/or executing validation activities and documentation for Computerized Systems, under respected regulations or guidelines: 21 CFR Part 11, 21 CFR Part 820, ISO 13485, GAMP 5,...

When you’re part of the team at Thermo Fisher Scientific, you’ll do important work. Surrounded by collaborative colleagues, you’ll have the support and opportunities that only a global leader can give you. Our respected, growing organization has an outstanding strategy for the near term and beyond. Take your place on our strong team and help us make...

About Nd Incorporated in 2007, we are a patient-centric solution provider for the pharmaceutical industry. We are experts in engineering consultancy, commissioning, qualification and validation services, and regulatory quality/compliance in Asia and Europe. We offer personalized focused solutions for the pharmaceutical industry in engineering consultancy...

Carecone PTE. LTD.Job Title: Software Hardware Validation TechnicianAbout Us:Carecone PTE. LTD. is a leading provider of computer system validation services. We are seeking a skilled technician to join our team.Responsibilities:Support computer SW/FW/Validation Engineering team for testing and validation.Perform computer setup and maintenance, including...

As a CSV Consultant, you will be working for our clients in the respect of the applicable regulations and quality procedures. The main assignments will be: Main assignments: - To be responsible for preparing and/or executing validation activities and documentation for Computerized Systems, under respected regulations or guidelines: 21 CFR Part 11, 21 CFR...

**Permanent Role**: - **Basic Salary Up to 7,000 + 2 months VB**: - **Working location: West MRT**: - **Pharmaceutical Industry Experience is a MUST**: - **CIP, SIP experiences will be preferred** **Responsibilities**: - Perform risk-based commissioning, qualification and validation service for pharmaceutical and biopharmaceutical clients on Process...

**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...

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 /...

Industry/ 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: Permanent **Key Responsibilities** - Assist Quality and Validation Manager Asia to complete the...

**As a computer systems validation specialist you will work as part of a multidiscipline team, supporting the design, construction, commissioning and qualification of new and modified pharmaceutical and life science facilities, equipment and processes.** **Responsibilities**: - Primary focused on Emerson DeltaV, Siemens PLC, MES, LIMS and Data Historian...