Batch Records Jobs in India

*Position:AGM/DGM - Production (Sterile Production – Cartridge)**Location: Vizag*Key Responsibilities:Manage endtoend sterile cartridge production operations.Ensure adherence to cGMP regulatory and quality standards.Plan schedule and monitor production activities to meet organizational targets.Lead...

Title:Quality Inspector - CatalystJOB TITLE: Quality Inspector CatalystREPORTS TO:Senior Technical Advisor QualityJOB LOCATION:Pune IndiaPOSITION SUMMARY: The Catalyst Quality Inspector is responsible for ensuring that KBR catalyst products consistently meet defined quality performance and regulat...

Mail:- 10Chemical Laboratory Analyst - Salary How to Become Job ...A Chemical Analyst identifies measures and interprets the chemical composition of substances working in laboratory settings within industries like pharmaceuticals manufacturing and environmental science. They are responsible for test...

Overview : We are seeking a dedicated and detail-oriented Executive Quality Control & Quality Assurance to join a leading cosmetics manufacturing company. The ideal candidate will be responsible for ensuring the quality of raw materials (RM) packaging materials (PM) and finished goods (FG) while su...

Position : Deputy Manager – QA IPQA (Sterile Injectable)Key ResponsibilitiesMonitor and control IPQA activities in sterile injectable manufacturing filling and packaging areas.Ensure adherence to aseptic practices gowning procedures and cleanroom behavior.Review and approve batch manufacturing recor...

Mail:- Production Supervisor Manufacturing Operations CTC: Rs. We are looking for a hands-on Production Supervisor to manage day-to-day operations on the chemical/pharma manufacturing floor ensuring safety quality and output targets are consistently met.Qualification / (Chemistry / Biochemistry)...

JOB DESCRIPTION:Minimum Qualification: M. Pharma/ B. Pharma/.Candiate shall be well versed with manufacturing and packaging operations Compression Machines Isolators Blenders Bulk packing lines & Process Validation. Followings will be the responsibilities of the position holder:To ensure complianc...

JOB DESCRIPTION:M. Pharma/ B. Pharma.Experience: 2 to Years Experience in solid dosage form- Tablets (Hormone)Person shall be well versed with manufacturing and packaging operations Compression Machines Isolators Blenders Bulk packing lines & Process Validation. Person with Experience in Hormone F...

We are seeking a Quality Assurance Engineer with experience in lyophilization systems to ensure compliance validation and quality excellence across equipment and processes. The role will involve working across the equipment lifecycle including exposure to Design Qualification (DQ) and Factory Accept...

We are seeking a Quality Assurance Engineer with experience in lyophilization systems to ensure compliance validation and quality excellence across equipment and processes. The role will involve working across the equipment lifecycle including exposure to Design Qualification (DQ) and Factory Accept...

REQUIREMENTSTotal experience: 4 yearsStrong experience in Siemens OpCenter Pharma (MES) with end-to-end implementationsMandatory experience in Recipe Authoring / MBR (Manufacturing Batch Record) designGood understanding of ISA S88 standards and batch process modelingExperience in designing operation...

We are seeking a Quality Assurance Engineer with experience in lyophilization systems to ensure compliance validation and quality excellence across equipment and processes. The role will involve working across the equipment lifecycle including exposure to Design Qualification (DQ) and Factory Accept...

Job Description: Plant Operator Role: Field Executive Grade: WL3 / WL5 Number of Positions: 3 Experience Required: 3-4 years Educational Qualification: ITI / Diploma / / (Regular mode of study) Preferred Industry: Agrochemical FMCG Oil Pesticide Paints PURPOSE The Plant Operator is responsible for...

Sterile Manufacturing Operations: Oversee aseptic filling compounding filtration and lyophilization processes to ensure product sterility and quality. Aseptic Practices & Compliance: Ensure adherence to GMP USFDA MHRA WHO and EU-GMP guidelines maintaining sterility assurance in cleanroom environmen...

Job DescriptionThe Manufacturing Execution System (MES) Specialist acts as a subject matter expert. The MES Specialists primary responsibility is to ensure that the deployment of the Werum/Korber PAS-X electronic Master Batch Records are successfully and compliantly designed developed deployed and s...