Qc - Validation Engineer

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...

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...

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....

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...

The Senior Validation Engineer is responsible for the qualification or requalification of laboratory equipment within the targeted schedule. **Responsibilities**: - Responsible for managing and writing of qualification related documentation but not limited to Qualification Plan and IQ, OQ, PQ and ERES Test Scripts for QC laboratory equipment (lab bench and...

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...

**Role Overview** We are seeking a QC Engineer with strong experience in **Computer System Validation (CSV)** for analytical laboratory instruments /equipment. The role ensures compliance with 21 CFR Part 11, data integrity, and global validation standards in a regulated GMP environment. **Key Responsibilities** - Lead CSV activities for **analytical...

Job Title and Industry Job Title: Benchtop IT / CSV Engineer – QC Laboratory Systems Industry: Life Sciences / Pharmaceutical Manufacturing Role Overview We are seeking a Benchtop IT / CSV Engineer to support validation and compliance activities for laboratory computerized systems and instruments used in QC and analytical environments. The role involves...

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...

Industry/ Organization Type: Chemical Manufacturing - Position Title**:QC Engineer**: - Working Location: Tuas - Working Hours: Monday - Friday, 8.30 am - 5.30 pm - Salary Package**:Up to $3,200 + Transportation Allowance + AWS + VB (Up to 4 months)**: - Duration: Permanent **Key Responsibilities** - Report directly to the section manager and HOD - Shall...