Qualification Validation Specialist

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...

**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...

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...

We are currently seeking for a QA Validation Specialist to support our client in Biopharma Industry. **Responsibilities**: - Review and approve all validation and qualification documentation related to Facility, Utilities and equipment, Computerize System and Automation and also QC Laboratory Equipment and System - Provide technical assessmemt to Change...

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...

**Responsibilities**: - 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 timely - Review and approve as needed, qualification/validation...

**As a computer systems validation specialist you will work as part of a multidiscipline team, supporting the design, construction, commissioning and qualification of new and modified pharmaceutical and life science facilities, equipment and processes.** **Responsibilities**: - Primary focused on Emerson DeltaV, Siemens PLC, MES, LIMS and Data Historian...

**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...

Job DescriptionSg Meinersen is seeking a skilled CQV Engineer to join our team in Singapore. The ideal candidate will have a minimum of 7 years of experience in equipment validation within the pharmaceutical industry.Key ResponsibilitiesDevelop and execute commissioning, qualification, and validation protocols for pharmaceutical equipment and systems.Ensure...

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...

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...

About the RoleWe are seeking a highly skilled and experienced professional to join our team as a Pharmacy System Technologist.The successful candidate will have a strong background in Life Sciences, Engineering, Information Systems, or Computer Systems.Diploma or degree holders are preferred, along with experience in equipment and systems commissioning,...

Key ResponsibilitiesThe Contract QC Specialist will be responsible for:Leading project for method validation/verification/transfer to introduce new/remediated QC methods for testing existing and new products independently.Ensuring timely release of methods to support commercial production, manufacturing investigations, and product investigations.Maintaining...

Pm Asia Project Services Pte Ltd is looking for a Systems Qualification Expert to support one of our many clients in the field of commissioning, qualification and validation work within the Life Sciences space.ResponsibilitiesPlan, Perform and Coordinate computer system validation, equipment qualification, temperature controlled objects (freezers, incubator...

We are seeking an SSD Validation Engineer to join our team at Micron Semiconductor Asia Operations PTE. LTD.About the RoleThis is a key position in our organization, responsible for performing firmware validation on solid-state drive (SSD) devices. The ideal candidate will have experience with protocols, Windows/Linux operating systems, Python, C++, test...

Job Description    At WUXI XDC SINGAPORE PRIVATE LIMITED, we are seeking a skilled Validation Associate Engineer to join our team. In this role, you will be responsible for participating in validation activities during the Commissioning & Qualification stage for our Singapore greenfield site and maintaining validation status after release.    Key...

We are Coalesce Management Consulting! A community of people with 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. Our approach is Simple but meaningful - We Grow by Helping Others Grow, We pride ourselves on providing...

**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...

We are a leading global company that develops cutting-edge autonomous driving technologies from Level 2 to Level 4. Our mission is to create safe and reliable driverless solutions that make mobility and transportation safer, more affordable, and accessible. We seek a skilled and passionate Self-Driving Technology Validation Specialist to join our research...

Join Our TeamWe are excited to announce that we are hiring a Quality System Specialist to join our team at Antaes Consulting SA. This is a fantastic opportunity for someone who is passionate about quality assurance and regulatory compliance.Main Responsibilities:Provide quality oversight for validation activities, ensuring compliance with regulatory...