Validation Engineer, Qc

We are looking for a QC Engineer to support **validation of analytical laboratory instruments and computerized systems**in a GMP-regulated environment. The role focuses on ensuring compliance with 21 CFR Part 11, Annex 11, ALCOA+ principles, and data integrity requirements. **Key Responsibilities**: - Plan, execute, and document qualification/validation of...

**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...

**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...

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...

**Responsibilities**: - Conduct cleaning validation activities with a specific emphasis on CIP for pharmaceutical manufacturing equipment and processes. - Develop and execute cleaning validation protocols, ensuring compliance with regulatory requirements and industry standards, especially in the context of procedures. - Collaborate with cross-functional...

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...

**Key **Responsibilities** Your responsibilities include, but are not limited to: - This position will support operational readiness of a new facility. - Establishment of QA Validation procedures (drafting and reviewing QA Validation functional SOPs). - Act as SME to develop commissioning, validation and qualification procedures, train and guide site...

Job OverviewWe are seeking a skilled Validation Specialist to support key validation activities within our Quality Control (QC) Laboratory. This role involves both software upgrade validation and the decommissioning of legacy computerized systems in a Good Manufacturing Practice (GMP)-regulated environment.Key Responsibilities:Plan and execute validation...

We are seeking a Computer System Validation (CSV) Engineer with around 5 years of relevant experience to support QC and laboratory operations in a regulated GMP environment. The role involves ensuring that computerized systems and laboratory equipment are validated, maintained, and compliant with regulatory standards, while supporting continuous improvement...