Validation & Qualification Engineer

Roles & ResponsibilitiesWe are seeking highly skilled Commissioning, Qualification, and Validation (CQV) Engineers to provide risk-based CQV services for pharmaceutical and biopharmaceutical clients. This role offers opportunities to work across various areas, including process equipment, CIP/SIP (Clean-In-Place/Sterilize-In-Place), and process manufacturing...

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

Job Description - Permanent Role - Basic Salary range from $4000 to $7,000 + 2 months VB - Pharmaceutical Industry Experience is a MUST **Responsibilities**: - Perform risk-based commissioning, qualification and validation service for pharmaceutical and biopharmaceutical clients on Process Equipment, CIP / SIP, Process Manufacturing and related business...

As a CQV Engineer, you will be responsible for ensuring the successful commissioning, qualification, and validation of equipment, systems, and processes within client’s pharmaceutical plant. You will play a crucial role in maintaining compliance with industry regulations, optimizing operational efficiency, and ensuring the quality and safety of the...

Job Description - Permanent Role - Up to $7,500 + 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 Equipment, CIP / SIP,...

**Process Engineering Specialists** **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...

ABOUT ARCONDIS Arcondis is a global consulting company with an exclusive focus on the healthcare and life science industries, with their particularly demanding requirements on quality and regulatory aspects. We have been managing challenges and solving problems for our clients in the areas of compliance, business processes, information technology, and...

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, -...

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 1,000 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 7,600 people spread across 5 continents and more than 60...

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 7,600 people spread across 5 continents and more than 60 countries....

**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...

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...

**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 /...

Job OverviewSg Meinersen is looking for an experienced CQV Engineer to join our team in Singapore. The ideal candidate will have at least 7 years of experience in equipment validation within the pharmaceutical industry.Key AccountabilitiesLead the development and execution of commissioning, qualification, and validation protocols for pharmaceutical equipment...

**Purpose**:Support equipment qualification, system qualification, and cleaning validation. **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. - Lead project validation activities, and...