Equipment Validation Engineer

We are looking for a highly skilled Equipment Validation Professional to join our team at Recruit Express Pte Ltd. In this role, you will be responsible for conducting routine reviews of qualification and validation processes and documentation, as well as ensuring timely calibration and corrective/preventive maintenance of equipment.The ideal candidate will...

PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors. With offices across Europe, Asia and US, our core focus is on consistently delivering high-quality outcomes for our multinational...

**About Us:**Recruit Express Pte Ltd is seeking a highly skilled professional to join our team as a Pharmacy System Technologist. As a key member of our team, you will play a crucial role in developing and executing equipment qualification and validation plans and protocols.**Responsibilities:**Develop and execute equipment qualification and validation plans...

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...

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, -...

**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 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...

**MAIN PURPOSE - To optimize existing processes (ie. yield, quality, efficiency) and to ensure that production goals are met. Maintain level of production and activities on an hourly, daily and monthly basis with strong engagement at shopfloor. - Develop key leading indicator metric and monitor performance of equipment, machines and tools, timely correcting...

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...

**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...

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...

**Position: QC Validation Engineer** At Coalesce Management Consulting, we are a community of people with a strong passion for excellence. We deliver bespoke project solutions within the Life Science and Technology sectors through our community of high-calibre industry specialists. We are currently expanding our team and are looking for a QC Validation...

1. Do validation test setup and verify that the setup is as per requirement 2. Perform product validation activities as per schedule. These includes - Endpoint functional test - Setup and verify test racks - Setup and verify monitoring racks - Execute EMC test 3. Data collection, processing and reporting 4. Ensure uptime of reliability test equipment during...

**Position: Quality Assurance Validation Engineer** We are Coalesce Management Consulting - a community of people with a strong Passion for Excellence. We deliver bespoke project solutions within Life Science and Technology sectors by Consultative through our community of High Calibre Industry specialists. We are currently expanding our team and are...

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...

**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 qualification execution and lead validation deviation investigation encountered in qualification. - Collaborate with multi functions...

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...

**Permanent Role**: - **Basic Salary Up to 7,000 + 2 months VB**: - **Working location: West MRT**: - **Pharmaceutical Industry Experience is a MUST**: - **CIP, SIP experiences will be preferred** **Responsibilities**: - Perform risk-based commissioning, qualification and validation service for pharmaceutical and biopharmaceutical clients on Process...