GMP Validation Manager

Roles & ResponsibilitiesQA Specialist (Validation/ GMP/ CAPA/ Pharma)12 Months ContractLocation: TuasUp to $5,000 depending on experienceIndustry: PharmaceuticalOur client aims at creating a new manufacturing concept consisting of a new generation of evolutive multi-product facilities, modular, adaptable, and agile, leveraging new disruptive technologies, to...

Roles & ResponsibilitiesQA Specialist (Validation/ GMP/ CAPA/ Pharma)12 Months ContractLocation: TuasUp to $5,000 depending on experienceIndustry: PharmaceuticalOur client aims at creating a new manufacturing concept consisting of a new generation of evolutive multi-product facilities, modular, adaptable, and agile, leveraging new disruptive technologies, to...

Job DescriptionWe are looking for a skilled GMP Compliance Expert to join our team at Recruit Express Pte Ltd. The successful candidate will be responsible for reviewing and approving engineering documents, participating in alignment meetings, and ensuring adherence to quality systems and GMP standards.Key Responsibilities:Review and approve engineering...

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...

About this Opportunity:Join us as a Financial Planning & Analysis Manager at GMP Group in Singapore! As a key member of our corporate office, you will play a crucial role in supporting our company's strategic goals through effective financial planning and analysis. If you have a passion for numbers and a drive to succeed, this could be the perfect...

Roles & ResponsibilitiesJob ObjectivesEstablish DSSG Quality Management System (QMS) in GMP QA through review and improvement of operational process, and ready for obtaining the importation license and new product launch. Promote GMP/GDP QA activities and enhance QMS. As a result, contributed to the stable supply of the highest quality products and DS's...

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...

We are looking for an experienced Regulatory Compliance Expert to join our QA team at Thermo Fisher Scientific. In this role, you will be responsible for reviewing and approving all GMP documents from functional teams and ensuring timely delivery of regulatory and client expectations.Your attention to detail and ability to identify and address quality issues...

We are looking for a skilled GMP Purchaser to join our team at This Is An IT Support Group. The successful candidate will be responsible for managing purchasing activities, including sourcing and procuring materials, supplies, and equipment necessary for our GMP facilities.Duties and Responsibilities:Manage purchasing activities, including sourcing and...

Roles & ResponsibilitiesHiring for fresh grads 2025Responsibilities● Participate in the validation activities during Commissioning & Qualification stage for Singapore greenfield site and be responsible for validation status maintenance after release.● Ensure compliance with appropriate regulatory and company requirements.● Responsible for drafting or...

**About Amaris Consulting**We are an independent technology consulting firm providing guidance and solutions to businesses.Our international team of 7,600 people spread across 5 continents and more than 60 countries has been rolling out solutions in major projects for over a decade.We strive to provide our candidates with the best possible recruitment...

Roles & ResponsibilitiesAdhere to safety protocols, policies, and procedures; address risky behaviours of self and others. Collaborate effectively with team members to complete work assignments. Perform repetitive tasks in a GMP environment, ensuring a clean workspace. Prepare reports such as daily pass-downs, track equipment inventory, and manage...

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...

The Consortium for Clinical Research and Innovation, Singapore (CRIS) brings together six national R&D, clinical translation and service programmes to advance clinical research and innovation for Singapore, and establish important capabilities for a future-ready healthcare system.As a Supply Chain Manager GMP at CRIS, you will play a key role in ensuring the...

About the RoleThis position involves providing high-quality oversight for validation, qualification, and replacement of manufacturing process equipment. You will assess and approve acceptance tests, reports, and documentation, ensuring compliance with relevant policies and standards.You will collaborate with cross-functional teams to plan, coordinate, and...

Key ResponsibilitiesProvide quality oversight for validation, qualification, and replacement of manufacturing process equipment.Assess and approve acceptance tests, reports, and documentation in line with policies and compliance requirements.Review and authorize engineering changes, deviations, and exceptions during validation activities.Work closely with...

About the JobAs a key member of our team, you will be responsible for providing quality oversight for validation, qualification, and replacement of manufacturing process equipment.You will assess and approve acceptance tests, reports, and documentation in line with policies and compliance requirements. Additionally, you will review and authorize engineering...

About the PositionWe are seeking a highly skilled Validation and Qualification Expert to join our dynamic community.The ideal candidate will have at least 5 years of experience in equipment validation within a GMP-regulated environment and a strong knowledge of cGMP standards and regulatory compliance for equipment validation.About the ResponsibilitiesAssess...