0.0 - 2.0 years

3 Lacs

Aurangabad

Work from Office

Feed tank operator- Capsules Organization Context Position Title: Feed tank operator Capsules Employee Name: Grade : Department: Mucilage preparation Location: Dahanu Reports to: Chemist and Shift supervisor Reported by: Job Objective Execute feed tank preparation process, timely filling of Feed Tank BMR with online documentation to meet first time right Feed Tank preparation for production requirements. Primary responsibilities Strategic Planning Activities: Core: GMP and over gown adherence to shop floor. Ensure safety by using appropriate PPE and safe practices. Execute the FT preparation as per Production requirement in a shift as per SOP. Ensure shift handover/takeover on the shop floor and hold accountability for any failures/challenges in the previous shift. Ensure compliance to the daily dipping schedule for FT preparation, color change, ZMICs for specific requirements for all upcoming batches. Prepare all feed tank as per procedure mentioned in SOP. Ensure shade compliance of prepared feed tank on Mac bath to ensure zero productivity loss in account of color shade variation. Cross checking feed tank viscosity whenever required. Ensure zero cross contamination and subsequent productivity loss due to wrong colourant and additive addition. Ensure minimum losses of Colourant and additive. Ensure 100% online documentation for FT BMR to meet the GMP requirements. Generate and affix in-process status label to FT to meet GDP requirements and for the ease of identifications/to avoid cross contamination Preparation of new shades to achieve FTR wrt to capsule shade and inform recipe correction to chemist if required. A) Key Result Areas First time right feed tank preparation by complying all relevant SOP as per schedule B) Key Interfaces Internal InterfacesExternal Interfaces Gel room, Quality and production Auditor, Customer and Visitor C) Competency Technical Competency T CompassLeadership Competency L CompassCompetencyLevelCompetency Level GMP Communication GDP Team working Measurement system Auto viscosity unit and Y stirrer Mac beth, Y stirrer Prepared By Date Signature

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Quality Control orbit writers (orbiTouch outsourcing Private Limited).

16.0 - 20.0 years

0 Lacs

ankleshwar, gujarat

On-site

You are being hired for the position of QC Head at our company based in Ankleshwar, Gujarat. As the QC Head, you will be responsible for ensuring the quality of all batches manufactured, overseeing the Quality Control department functions, and managing activities related to quality assurance. Your main duties will include sampling, inspection, and testing of raw materials, packaging materials, in-process products, and finished products as per specifications for release or rejection. You will also be in charge of stability chamber handling, stability testing, and evaluation of shelf-life of products, as well as preparing stability testing protocols and reports. In addition, you will conduct microbiological analysis of raw materials, finished products, water, and environmental bio-burden monitoring. You will review monthly trend reports for physicochemical and microbiological data and ensure compliance with predefined specifications. Analytical investigations for complaints, product recalls, out of specification results, and deviations will also fall under your purview. Furthermore, you will be responsible for internal Quality System audits, quality review, analysis of non-conforming products, reference standards, working standards, and solution preparations. You will plan and manage all activities of the Quality Control Department to assure the quality of all products manufactured by the company. Coordinating with the manufacturing department to control processes and products at every stage of manufacturing will also be part of your role. Moreover, you will work on the development of specifications and analytical procedures in coordination with the Quality Assurance Department and R&D. You will review the adequacy and relevance of specifications and analytical procedures, ensure instrument qualification, implement audit trail systems for data integrity and security, and coordinate technical audits of the Quality Control Laboratory. Your responsibilities will also include maintaining Quality Control records, control samples, release records, routine Good Laboratory Practices auditing, organizing training programs, establishing guidelines and procedures on cGMP and Good Laboratory Practice, and evaluating Change Control suggestions for overall reviews and validations. As the QC Head, you will play a key role in upholding quality standards, ensuring compliance with regulations, and contributing to the continuous improvement of quality control processes within the company.,

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