Junior Validation Engineer

Roles & ResponsibilitiesKey Responsibilities: Review of P&IDs during commissioning phase Generation of Change control and System Impact Assessment (Kneat) Review vendor documents for completeness Provide SAT support Validation document generation and protocol for equipment, including, but not limited to, process equipment and utility systems, both paper...

Roles & ResponsibilitiesAs a Validation Engineer, you play a pivotal role in our organization by ensuring that each product release surpasses quality expectations. Your responsibilities encompass understanding potential system failures, designing validation scenarios, and driving continuous improvement initiatives. Acting as a gatekeeper in a dynamic product...

Roles & ResponsibilitiesAs a Validation Engineer, you play a pivotal role in our organization by ensuring that each product release surpasses quality expectations. Your responsibilities encompass understanding potential system failures, designing validation scenarios, and driving continuous improvement initiatives. Acting as a gatekeeper in a dynamic product...

POSITION SUMMARY Incumbent will be responsible for leading product manufacturing campaigns from the start of production, and providing technical supervision with respect to quality and EHS until completion and release of the material.POSITION RESPONSIBILITIESDevelop Manufacturing/Operating Instructions and necessary Standard Operating Procedures.Develop,...

Roles & ResponsibilitiesJob Summary:The Validation Engineer is responsible for ensuring that medical devices and manufacturing processes meet required quality standards and regulatory requirements. It includes lead and/or execute validation activities, including equipment, process, test method and software validation, to ensure that products are manufactured...

Roles & ResponsibilitiesJob Summary:The Validation Engineer is responsible for ensuring that medical devices and manufacturing processes meet required quality standards and regulatory requirements. It includes lead and/or execute validation activities, including equipment, process, test method and software validation, to ensure that products are manufactured...

Today, Lonza is one of the world’s largest healthcare manufacturing organizations operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers....

Roles & ResponsibilitiesJob Description & RequirementsJob Description: 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...

Roles & ResponsibilitiesJob Description & RequirementsJob Description: 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...

Roles & ResponsibilitiesThe OpportunityEsco Lifesciences Group is Singapore’s most globalized life sciences company, with annual revenues close to SGD 200M and global operations in over 42 locations and 26 direct countries across North America, Europe, Asia, Oceania.Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first incorporated in...

Roles & ResponsibilitiesResponsibilities: Develop and execute Commissioning, Qualification, and Validation (CQV) protocols (IQ/OQ/PQ) for pharmaceutical manufacturing facilities, equipment, and systems. Collaborate with project teams to ensure compliance with regulatory standards (e.g., FDA, EMA, GMP). Perform risk assessments, gap analysis, and prepare...

Roles & ResponsibilitiesResponsibilities: Develop and execute Commissioning, Qualification, and Validation (CQV) protocols (IQ/OQ/PQ) for pharmaceutical manufacturing facilities, equipment, and systems. Collaborate with project teams to ensure compliance with regulatory standards (e.g., FDA, EMA, GMP). Perform risk assessments, gap analysis, and prepare...

ANTER CONSULTING PTE. LTD.Salary: $80,000 - $110,000 per annumAbout the RoleWe are seeking a Junior Validation Engineer with 0-3 years of experience to support validation activities, ensuring compliance with regulatory and quality standards, especially GMP. The role involves collaboration with cross-functional teams to meet project goals.Key...

Today, Lonza is one of the world’s largest healthcare manufacturing organizations operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers....

Roles & ResponsibilitiesPharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world...

Roles & ResponsibilitiesPharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world...

About the Role:The Process Validation Engineer will be responsible for providing process validation support for Takeda vaccines manufacturing operations located in internal and CMO manufacturing locations. This includes overseeing process validation activities, developing and authoring process validation strategies, and ensuring compliance with cGMP...

OverviewAmaris Consulting, a global technology consulting firm, offers expertise in various business lines, including Information System & Digital, Telecom, Life Sciences, and Engineering.Estimated Salary Range: $80,000 - $110,000 per annumJob DescriptionThe ideal candidate will possess strong coding skills and experience in configuring DeltaV systems....

Roles & ResponsibilitiesMeet the TeamSilicon Labs is seeking experienced validation engineer for a new IoT MCU Validation team. The ideal candidate is an enthusiastic detail-oriented system level engineer with a solid understanding of low power MCU architectures in terms of both digital and analog aspects. The position also requires software proficiency at...

Roles & ResponsibilitiesMeet the TeamSilicon Labs is seeking experienced validation engineer for a new IoT MCU Validation team. The ideal candidate is an enthusiastic detail-oriented system level engineer with a solid understanding of low power MCU architectures in terms of both digital and analog aspects. The position also requires software proficiency at...