Officer / Sr. Officer - Quality Assurance-API -Pharma Industry -Vapi GenNext India Private Limited

1.0 - 6.0 years

2 - 4 Lacs

Vapi

Work from Office

Should have the experience in activities like QMS Activity, BMR Review, Change Control, Document Issuance, Vendor Qualification, Process Validation etc. Process validation / equipment Qualification protocol preparation and review Required Candidate profile Vendor qualification and validation

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Deputy Manager - Stores Dishman Carbogen Amcis Ltd

5.0 - 9.0 years

0 Lacs

gujarat

On-site

As Deputy Manager - Stores at Dishman Carbogen Amcis Limited located in Bavla, Gujarat, IN, you will be responsible for overseeing various key activities. Your role will involve managing Quality Management System (QMS) activities, ensuring compliance with Current Good Manufacturing Practices (CGMP), handling regulatory and customer audits, and overseeing the formulation warehouse operations independently. Additionally, you will be tasked with managing all activities of the Raw Material (RM) warehouse, including receipt, storage, and dispensing, as well as overseeing finished goods and dispatches for both domestic and export purposes. The ideal candidate for this role should possess strong managerial skills, a solid understanding of compliance requirements, and experience in warehouse management. You should be capable of handling legal aspects related to warehouse operations and have a background in manufacturing. This position offers the opportunity to take on a challenging role in a dynamic environment where you will play a crucial part in ensuring operational efficiency and regulatory compliance.,

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QA Executive Nutrition Shoppe

2.0 - 6.0 years

0 Lacs

punjab

On-site

As a QA Executive, you will be responsible for various quality assurance tasks including Change Control, Deviation, Out of Specification, Market Complaint, Corrective and Preventive Action (CAPA), and Annual Product Quality Review. Additionally, you will be involved in Audit Compliance Report Preparation, Label compliance, Legal Metrology (Packaged Commodities), FSSAIs Labelling and Display Regulations, and implementation of GMP/GHP requirements in the food industry. You will be required to manage Calibration activities both internally and externally, Equipment Qualification & Documentation control, Process Validation Protocol & Report Preparation, and Cleaning Validation Protocol & Report Preparation. Monitoring and compliance of Self-Inspection and Quality Audits, Technology Transfer activities, HACCP preparation and monitoring, QMS activities, Food safety-related activities, and training execution will also be part of your responsibilities. Furthermore, you will oversee the checking of Building and Facility, Equipment, HVAC System, and Process Validation. Managing GMP and Quality Documents, including CQPs & SOP's, Protocol and Reports, Formats, Logs and Log Books, and Batch Record will also be part of your duties. In this role, you will also monitor and review Reprocess and Recovery in manufacturing areas, ensure GMP Compliance in the plant on a daily basis, and coordinate with various stakeholders to maintain quality standards. This is a full-time position with benefits such as health insurance. The work schedule is during the day shift. The ideal candidate should have at least 2 years of experience in QA/QC, Quality assurance, Quality management, CGMP, Food safety, Food industry, and HACCP. Please note that the work location for this position is in person.,

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Unit QA System Coordinator - Female Preferred Transcend Human Resource Services

7.0 - 12.0 years

7 - 10 Lacs

Bharuch, Palej

Work from Office

Prepare schedule, direct, & perform internal audits Prepare schedule, analyze report, & discussion Establish & maintain KPI, performance mgt against set goals Create custom reports to analyze, form decisions Implementing QMS, EMS & OH&SM

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