QMS Coordinator - Dehra Dun, Uttarakhand

Company Description · Encraft India Pvt. Ltd., a part of the DCJ Group established in 1961, specializes in manufacturing innovative thermoplastic engineering products. The company focuses on precision-engineered uPVC Door & Window systems that combine durability, style, and secur ...

We are seeking a Senior SAP PP & QM Support Consultant with strong hands-on experience in manufacturing and quality management production support. · Provide L2/L3 production support for SAP PP processes including: · Demand Management (PIRs) · MRP (Classic MRP / MRP Live) · ...

The Quality Manager is responsible for ensuring that all quality-related activities are carried out in accordance with regulatory requirements and good manufacturing practices (GMP). They will prepare and review standard operating procedures (SOPs), batch manufacturing records (B ...

Role & responsibilities · Ensure compliance with cGMP, WHO-GMP, USFDA, MHRA and other regulatory guidelines · Review and approve BMR/BPR, SOPs, STPs, Specifications, Protocols, and Validation Reports · Handle Deviations, OOS, OOT, Change Control, CAPA, and root cause investigatio ...

What we re looking for · Experience Required 12/18 months of experience for ITI holders, 24/36 months-non-ITI Holders. · Educational Qualification ITI in electrical/electronic/Fitter discipline/Mechanical or 10+2 with Experience in Automation handling operation · Good handling ra ...

The position of machine operator is responsible for the safe and efficient operation of rapid diagnostic card device assembly and packaging machines across all rolling shifts. · ...

The Opportunity · The Opportunity: · Machine Operator is responsible for safe, compliant, and efficient operation of rapid diagnostic card device assembly and packaging machines across all rolling shifts. This requires strict adherence to GMP, ISO (13485/9001:2016), and shopfloor ...

Machine Operator is responsible for safe, compliant and efficient operation of rapid diagnostic card device assembly machines across all rolling shifts. · ...

We are seeking a detail-oriented Quality Documentation officer to manage quality-related documents in compliance with company standards and regulatory requirements. · ...

We are looking for a Quality Engineer with expertise in QMS,IATF,VSA,VDA,MSA and MACE for our Rudarpur location. The ideal candidate should have experience in customer coordination,supplier quality management and internal audits within a manufacturing environment. · Customer Coor ...

Job descriptions may display in multiple languages based on your language selection. · What We Offer · At Magna, you can expect an engaging and dynamic environment where you can help to develop industry-leading automotive technologies. We invest in our employees, providing them w ...

Manages audit and compliance. Reviews documents related to FSSC 22000 and SOPs in E-DMS. · ...

Plan and monitor analysis of sample, lead laboratory investigation, · conduct effective review of team and portfolio provide direction and guidance to the team · and develop team competence with the objective of ensuring release of batches with adherence to GMP compliance · and q ...

Job Title: Research Associate- DQA · Name of Dept: Research & Development · Key Responsibilities: · Impart training on cGMP, GLP, behavioural, motivational, and compliance-related programs to ensure adherence to specified procedures and regulatory guidelines. · Handle and manage ...

Job Description · SAP MDM · . · Preferred candidate profile · Key Responsibilities · Create, maintain, and update Master Data in SAP (Material Master, BOM, Inspection Plan, Vendor Master, Customer Master etc.). · Ensure data accuracy, completeness, and consistency as per company ...

At Sun Pharma we commit to helping you create your own sunshine by fostering an environment where you grow at every step take charge of your journey and thrive in a supportive community. · ...

Plan and monitor analysis of sample, lead laboratory investigation, conduct effective review of team and portfolio. · ...

Plan and monitor analysis of sample, lead laboratory investigation, conduct effective review of team and portfolio, provide direction and guidance to the team and develop team competence with the objective of ensuring release of batches with adherence to GMP compliance and qualit ...

+Plan and monitor analysis of sample, lead laboratory investigation, conduct effective review of team and portfolio, provide direction and guidance to the team and develop team competence with the objective of ensuring release of batches with adherence to GMP compliance and quali ...

Sr. Executive position at Sun Pharma in Paonta Sahib to ensure GMP compliance on shop floor and lead a team. · ...