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Quality Manager Graduate Experience Jobs in Nainital

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  • 8 - 10 yrs
  • Kaladhungi Road Nainital
Quality Assurance Systems Equipment Qualification
Were looking for an who doesnt just follow quality systems, but strengthens them. : Nayagaon, Kaladhungi, Nainital, Uttarakhand : B. Pharma / M. Pharma : 78 years of relevant experience in Quality Assurance : Negotiable : Develop, prepare, and review Standard Operating Procedures (SOPs) Interpret and implement quality assurance standards and procedures Assess the adequacy and compliance of QA standards Manage the preparation, issuance, revision, and retrieval of documents Review the implementation and effectiveness of quality and inspection systems Demonstrate strong knowledge of CAPA, deviation management, change control, and Root Cause Analysis (RCA) Implement and execute the Quality Management System (QMS) in alignment with industry standards Ensure shop floor compliance with SOPs and regulatory expectations Oversee validation and qualification activities for processes, instruments, equipment, and facility Qualification (equipment, utility & audit compliance) Knowledge and application of FSSAI, FSSC 22000, HACCP, and FEMA standards Conduct training programs and assess training effectiveness Ensure compliance with global regulatory standards such as 21 CFR, WHO GMP, and UMP
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Manager-Quality Assurance

Bajrang Placement Services

Quality Assurance Manager Quality Assurance Incharge Quality Assurance Executive Quality Assurance Analyst Quality Assurance Member
Position: Manager-Quality Assurance Location- Kaladhungi, NainitalExperience- Minimum 8-10 Years Experience in Herbal Extract, Pharmaceutical, Nutraceutical. Person shall be well versed QMS elements, review of documents, and Microsoft Office Word/Excel.Salary- Negotiable + Travel AllowanceJob Description To follow and ensure the GMP & GLP rules and regulation all label of the plant. To ensure the implementation of the quality system in the plant and premises. Releasing or rejecting all raw materials, packing material, in-process and finished products. Establishing a system to release or reject raw material, intermediates, packaging and labeling materials. Approving all specifications and master production instructions. Approving all procedures impacting the quality of the products. Approving raw material, packing material vendors, contract laboratories and external agencies. Documentation Control: maintenance and updating of documents in compliance with regulatory requirements and implementation of Good Documentation Practices. To Lead, direct and develop QA team and also to lead HACCP Team. To assure Personal Hygiene and Health Check up shall be done as per SOP. To ensure the investigation of deviations, market complaints, returned goods, product recalls are done as per SOP. To remain all time alert and responsible to ensure truthfulness of data. Responsible for Tracking and implementation of Corrective and Preventive actions. To assess and approve annual product quality review report. Responsible for approval of qualifications, cleaning validation and process validation stability protocols/reports. Responsible for the approval of SOPs, Batch manufacturing record and other GMP documents as per the procedure. To ensure self inspection shall be done as per SOP. To conduct, execute and implement the training system as per SOP. To coordinate domestic and global GMP/Regulatory audits. To Approve change controls/ Devi
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