Validation Engineer

Job Description The Validation Engineer is responsible for ensuring that medical devices and manufacturing processes meet required quality standards and regulatory requirements. It includes leading and/or executing validation activities, including equipment, process, test method, and software validation, to ensure that products are manufactured consistently...

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...

**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...

**Mission Description** Supporting with execution of validation strategy during and leading up to shut down period (november'24 to Jan'25) in AMS **Profile Requirement** - Field experience with validation engineering - Execution of validation, validation test, qualification test - Have performed IQ and OQ and cleaning validation knowledge - Worked with...

Validation engineers manage, inspect, calibrate, test and modify the instrumentation, equipment, mechanics and procedures used in manufacturing. A critical aspect of their job is documenting this process so there is evidence that systems are operating safely and efficiently. Validation engineers can be found in a range of industries, including aerospace,...

**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 timely fashion. - Manage...

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...

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...

**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 -...

**Key responsibilities**: - Perform Process Validation activities. 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 equipment and associated validation activities to ensure compliance with regulatory requirements - Program, organize, and maintain...

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, -...

**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 /...

Responsibilities: - Responsible for executing and closing out the validation activities within the assigned area. - Develop or support the development of required validation documents, including Risk Assessments, plans, protocols, and reports. - Support the review, analyse, interpret and summarise data of executed studies. - Investigate or support the...

**Responsibilities**: - 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 validation...

Division - Automation - Funktion - Technik - Verwandter Standort - Singapur, Singapur **Making complexity accessible**: Mikron Automation is your worldwide partner for advanced automation solutions. At Mikron we are committed to delivering the best assembly systems and all needed services throughout your product’s entire life cycle. With our extensive...

**Main Responsibilities：** 1. Assist Quality and Validation Manager Asia to complete the tasks in time with good quality. 2. Responsible for successful execution the Validation functions for customer project, as required - Quality, Cost, Time. 3. Responsible to drive and support project team for projects where validation is required and ensure execution...

We are currently expanding our team within our Life Sciences Division team and are looking for a **Validation Engineer**to support projects on site with a client. The following are key responsibilities: - Review and approval of computer system validation protocols and reports. - Preparation and management of CSV deliverables for laboratory instruments and...

Pfizer Singapore is recruiting permanent employees for manufacturing site expansion of Pfizer Asia Manufacturing Pte Ltd (PAMPL) in Singapore. Use Your Power for Purpose Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is crucial to ensuring that customers...

**Job Title: Senior Validation Engineer** **Reports to: Manager** **Department: Process and Equipment Engineering** Location: Singapore, Gul Circle **Requisition ID**: **How Will You Make an Impact?** At Thermo Fisher Scientific, we have an incredible mission: to enable our customers make the world healthier, cleaner, and safer. Our responsibility in...