Equipment Validation Professional

**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...

Job description About the job Supports Validation activities related to validation of facility, equipment and utilities. Support day-to-day Validation activities in accordance with approved Validation SOPs/Plan/Policies. Develop & execute Validation Protocols and Reports, including supporting site discrepancies and deviations...

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 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...

**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...

**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 -...

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...

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...

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...

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, -...

Preparation and review of qualification documents e.g., User requirement specification, DQ, IQ, OQ and PQ protocol for equipment, utilities & facility in compliance with the regulatory guidelines. - Execution of qualification and validation activities including process, cleaning, computer system, equipment, utilities, and facility. - Preparation and review...

Company Description **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...

: PM Group is looking to expand the CQV team. This role will be supporting one of our pharmaceutical clients in the field of commissioning, qualification and validation work. : - Generation and execution of validation protocols and reports (including IQs, OQs, PQs, QAPs, etc.). - Working as a seconded PM Group resource in a client-led team. - To lead and/or...

**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...

**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...

**Responsibilities**: - Create and refine validation protocols for GxP critical reports, focusing on Computerized Equipment Validation within the QC lab. - Configure static Master Data for validated/GMP-compliant LabWare LIMS (version 6), specifically emphasizing Computerized Equipment. - Actively participate in executing, reviewing, and approving...

Job description About the job Provide Quality oversight to equipment/system qualification, automation qualification (PCS/BAS) and cleaning validation. Review and approve validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines in a timely manner. Review and approve as needed,...

Validate and qualify parts, processes and products as requested to ensure compliance to QMS. - Implement and follow-up of CAPA and Process Change Control systems. - Create cleaning validation protocols for PQ - Approval and review of all Data Integrity - Serve as Point of Contact for QA Validation - Review and approve all validation/qualification documents...