Qc Method Validation

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...

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...

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. Position: QC Validation Engineer Job Description: We are currently expanding our team and are looking for a QC...

Overview QC Associate - System Support (Equipment Qualification/ Validation/Pharma)Location : Gul Circle Salary Up to $4,500 depending on experience Completion Bonus 1 Month Our client delivers vital healthcare solutions worldwide, powered by the precision and dedication of its Manufacturing & Supply teams. With your talent, they can expand their...

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...

A leading recruitment agency is seeking a QC Expert for lab validation in Singapore. This role requires a university degree and 5 years of quality control experience in the pharmaceutical industry, focusing on compliance with regulatory standards. Responsibilities include maintaining validation plans, supporting inspections, and ensuring adherence to cGMP....

**Responsibilities**: - Support equipment, critical reagent and method transfer related qualification activities - Support setting up and maintenance of cell lines used for bioassays and support method - Participate in bioassay/QC related routine and non-routine activities according to Standard Operating Procedures such as product sample testing to meet...

As a Senior QC specialist supporting our clinical trials in Singapore and abroad, you will be part of a team responsible for ensuring patient safety through testing of our therapeutic product and its intermediates. You will also be expected to actively participate in assay development and validation, as well as in OOS, RCA, CAPA implementation, and may be...

**Why Patients Need You**: Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through...

384512BR **QC Analyst III**: Singapore **About the role** QC Analyst III Location - Singapore #LI Hybrid About the Role: This role will ensure proper maintenance of QC IPC/DS (In Process control/Drug Substance) lab equipment and systems and troubleshoot to ensure full cGMP-compliance for shift team. Key Responsibilities: - Perform product testing and...