Senior 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...

**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...

**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...

Job description About the job Supports 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...

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 & 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...

**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 Marvell At Marvell, we believe that infrastructure powers progress. That execution is as essential as innovation. That better collaboration builds better technology. Trusted by the world’s leading technology companies for 25 years, we move, store, process and secure the world’s data with semiconductor solutions designed for our customers’...

**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...

**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...

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...

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...

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...

Roles & ResponsibilitiesJob Responsibilities:MVP Matrix Update Software Assessment Spreadsheet Assessment Software Validation Package: MVP ( Individual Software Master Validation Plan ) SRS 21 CFR Part 11 Assessment FMEA IQ / OQ / PQ Protocol IQ / OQ / PQ ReportProcedure / Form Update New Software Development Plant Improvement Projects FDA...

Responsibilities/Job Scope: - Pre-silicon verification and post-silicon system validation - Test case and test automation scripts development and test plan execution - Debug system (hardware, software and firmware), provide expert support to internal as well as external customer - Silicon characterization and failure analysis - Booting and other source code...

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...