QMS Production - Paonta Sahib

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 ...

To ensure delivery of products on time, · of desired quality and quantity at optimum cost. · ...

Exhibit self-drive as you 'Take charge' and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we 'Thrive together' and support each other's journeys. · Investigation and overall handling of deviations, OOS, OOT and Market Complaints. · Review an ...

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 ...

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. · ...

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. · ...

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

+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 ...

To create your own sunshine by fostering an environment where you grow at every step and take charge of your journey. To prepare investigation reports for OOS, OOT, product quality complaints and unplanned deviations related to manufacturing. · To follow SOPs and perform tasks as ...

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) · ...

Responsible for Line Clearance, Knowledge of Quality SOP, SOP implementation and adherence at Shop Floor, BPR & BMR verification, QMS Documentation, Closely working with Production team for making Quality Products for Personal Care, Aerosol etc. · ...

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 ...

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 ...

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 ...

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 ...

Responsible for development, implement and strengthen the Quality system. · 2. · Review and approval of critical quality documents viz. Site master file, Validation Master Plan, Validation · Protocols & Reports,  Master MCM/MCP/BMR/BPR, etc. · 3. · Review and approval of Change C ...

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. · ...

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 ...