Computer System Validation Specialist Avon Quality Management

2.0 - 6.0 years

0 Lacs

delhi

On-site

We are seeking a skilled Computer System Validation (CSV) Specialist to join our team and assist clients in validating quality management system (QMS) software within the life sciences industry. Your main focus will be to ensure that the QMS software solutions meet regulatory requirements and industry standards, supporting clients in achieving compliance with Good Manufacturing Practices (GMP), FDA, EMA, and other applicable regulations. This client-facing role requires strong technical expertise, regulatory knowledge, and excellent communication skills. In this role, your responsibilities will include leading the validation of QMS software for clients, encompassing planning, execution, and ...

Posted 2 weeks ago

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Pharmaceutical Qualification SME Quascenta

2.0 - 6.0 years

0 - 0 Lacs

chennai, tamil nadu

On-site

The position is based out of Chennai and does not offer a remote work option. The salary offered is between 5-8 lacs CTC based on validation experience. At Quascenta, we specialize in providing comprehensive validation lifecycle management software solutions. Our mission is to empower pharmaceutical manufacturing sites by offering software tools to streamline product manufacturing and cleaning processes, ensuring compliance, efficiency, and savings. Our flagship products, such as eResiduePro, eProcessPro, and eLogBook, aim to transform how companies manage their product, process, and cleaning lifecycles. With over 20 years of experience, our solutions help organizations meet regulatory requi...

Posted 1 month ago

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Assistant Manager Motherson Automotive Technologies and Engineering (MATE)

3.0 - 7.0 years

5 - 9 Lacs

Noida

Work from Office

Identify/implement process improvement initiatives using Lean,Six Sigma,Kaizen methodologies. Analyze performance metrics/lead root cause analysis (RCA)/corrective action plans. Collaborate cross-functionally to reduce waste/increase efficiency. Required Candidate profile 3--7 years of experience in a quality or process engineering role. Strong understanding of ISO 9001, IATF 16949, and APQP. Hands-on experience with quality tools (5 Why, Fishbone, SPC, MSA, etc.).

Posted 3 months ago

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