Validator

Validation Lead GCF Grade Level: 05 Site: Amgen Singapore Manufacturing (ASM) **Role Description** Amgen discovers, develops and delivers innovative human therapeutics. A biotechnology pioneer since 1980, Amgen was one of the first companies to realize the new science’s promise by bringing safe, effective medicines from lab, to manufacturing plant, to...

**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 & 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...

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...

**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...

Roles & ResponsibilitiesKleen-Pak Products Pte Ltd is a trusted manufacturer of premium wet wipes and liquid hygiene products, serving global brands across sectors including retail, healthcare, F&B, and more. Our production facilities in Singapore and Vietnam are certified to ISO 9001, ISO 13485, GMP, and MDR standards, ensuring the highest quality. As part...

Roles & ResponsibilitiesKleen-Pak Products Pte Ltd is a trusted manufacturer of premium wet wipes and liquid hygiene products, serving global brands across sectors including retail, healthcare, F&B, and more. Our production facilities in Singapore and Vietnam are certified to ISO 9001, ISO 13485, GMP, and MDR standards, ensuring the highest quality. As part...

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...

**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...

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...

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...

Job description About the job 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 in a timely manner. Review and approve as needed,...

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...

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, -...

Company Description **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...

Company Description **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...

Roles & ResponsibilitiesAs a Validation Engineer, you will ensure that the manufacturing processes and products meet internal and external quality standards. Your role will involve developing and implementing validation protocols, analyzing data, and collaborating with cross-functional teams to maintain compliance and drive continuous improvement.Key...