Average salary: Rs246,856 /yearly
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- ...uniformity appearance) to ensure coating quality. Carry out equipment cleaning setup and changeover in line with SOP and validation. Document BMR entries logbooks and cleaning records as per GDP/GMP compliance . Coordinate with engineering/QA teams for troubleshooting...SuggestedFull time
- ...SOPs. Perform and record in-process checks ensuring compliance with BMR and GMP. Maintain logbooks cleaning records and documentation as per GDP standards. Adhere to safety protocols gowning procedures and cleanroom discipline . Coordinate with QA and maintenance...SuggestedFull time
- ...requirementХ Tracking Approval rate & other critical SLA deliverables for Gold loan product. Х Supporting Assayer in Operations /documentation. Required Qualifications and Experience Х Graduate with 1-3 years of relevant experience.Х Knowledge of Cross Sell / Gold Loan...SuggestedFull time
- ...Onboarding & Induction: Manage pre-joining formalities documentation and background verification. Conduct induction programs and coordinate functional onboarding with departments. Employee Life Cycle Management: Handle confirmations probation extensions transfers...SuggestedFull time
- ...CIPET in Plastic Technology Skills & Knowledge Necessary · New product development. · Knowledge of preparation of ISO Documentation · Ensure Safe use of equipments. · Train new employees to use safety guidelines and company standards. · Customer...SuggestedFull timeLocal area
- ...batch operations according to BMR parameters tablet weight hardness thickness and appearance. Conduct in-process checks and document results in BMR/logbooks as per GDP. Carry out machine setup cleaning lubrication and changeover between batches. Report and coordinate...SuggestedFull time
- ...manufacturing : granulation compression coating filling sterilization filtration. Verification of batch records log books and online documentation . Ensure compliance with SOPs GMP and regulatory guidelines (USFDA MHRA WHO EU etc.) . Handle deviations change controls...SuggestedFull time
- ...Root Cause Analysis: Conduct detailed investigations and impact assessments for deviations and process discrepancies. Documentation & Review: Ensure timely preparation and review of SOPs risk assessments and quality records in line with GMP. Audit Compliance...SuggestedFull time
- ...Control and Reporting: Allocate incoming samples to qualified microbiologists for various microbiological analysis ensuring proper documentation and traceability. Oversee the entire batch release process from analysis through to the final reporting of microbiological test...SuggestedFull time
- ...compliance with cGMP and applicable regulatory guidelines (USFDA EMA MHRA WHO etc.). Experienced in preparing and reviewing QMS-related documents such as SOPs CAPA deviations change controls Risk assessment validation protocols and reports. Proficient in MS Word MS Excel SAP...SuggestedFull time
- ...Data and Documentation Review: Perform rigorous independent review of analytical raw data calculations instrument audit trails and final reports (including OOS and deviation investigations) to ensure compliance with quality standards (ALCOA). Compliance Oversight: Review...SuggestedFull time
- ...evolving global chemical and polymer regulations. Timely and updated MIS shared with stakeholders Manage regular compliance documentation Prepare and manage MSDS, TDS, Regulatory Declarations, and customer-specific compliance documentation. Accurate and timely...SuggestedFull timeSide jobLocal area
- ...sealing inspection and serialization machines . Review and maintain Batch Packing Records (BPRs) logbooks and line clearance documentation . Coordinate with QA Engineering and Warehouse teams for smooth batch execution. Ensure in-process quality checks and compliance...SuggestedFull timeTraineeship