Validation Engineer — Lead Protocols, Risk

Contributes to validation planning and assists with carrying out medium- to large-scale projects that require customized, risk-based execution strategies, problem investigations, and troubleshooting while meeting project timelines. Utilizes expertise and input from Subject Matter Experts to perform effective risk assessments and develop experimental designs...

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...

Role Title: Validation Engineer (BioPharma) Duration: 1 year contract **Responsibilities **. - Support project execution from Feasibility through to project completion/handover, including all project stages such as: - Feasibility - Concept Design, Basic Design, Detailed Design - Commissioning & Qualification - Prepare/perform/review process engineering...

**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...

Salary Up from $4000 to $7,000 + 2 months VB - Pharmaceutical Company located at West - 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 Manufacturing and related business processes...

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

**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...

Commissioning, Qualification and Validation Engineer Remarkable people, trusted by clients to design and advance the world. Wood is currently recruiting for a Commissioning, Qualification and Validation Engineer to support our growing operations in Singapore. You will be responsible for the execution of project work in accordance with company procedures...

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, -...

No Deviation is a provider of patient-centric solutions for the pharmaceutical industry, and we are currently seeking individuals who are passionate about joining our team. Our areas of expertise include engineering consultancy, Commissioning Qualification Validation (CQV), as well as Quality, Compliance, and Regulatory services. We strongly uphold our core...