Qc Manager

Role & responsibilities

Job Profile

• Quality Assurance plan: Define QAP for Process/ Product and designs, Quality process adherence audit and ensuring strict compliance.
• Quality checks: Ensure inspection of raw material, packing material, consumables material checking, Ensure WIP check, Ensure Final quality monitoring, Review NCRs and recommend CAPA, Implementing CAPA recommendations and recommend trainings required
• Identifying and resolving in-house quality related issues to minimize incidences of rejections/reworking.
• Audit of QC processes: Quality audit process to assess quality plan adherence & staff competence, Coordinate with customers or external auditors, Coordinate with departments for implementation of audit requirements, QMS audit as per certifications, MR for audits
• Identifying requirements of various inputs for lab operations and ensuring availability there off
• Established healthy business relations with the clients & associates for securing long term customer loyalty, working towards solving their queries and complaints efficiently and educating Customers regarding product applications.
• Taking appropriate quality measures including preparation / maintenance of necessary documents and conducting audits to ensure compliance with standards
• Tracking of technical queries, regulatory deficiencies, change controls/deviations through database.
• Interpreted test data to determine if products meet specification and certifying products for sale to end customers.
• Tracking customer’s feedback on quality aspect and driving initiatives to introduce improvements.
• Quality Resource Planning: Instruments, manpower and facilities that might be required or to be upgraded
• Providing training on Quality System to new recruits and other personnel in operations.
• Planning and management on Operational Expenditure and Capital Budgets for testing.
• Necessary actions for product approval and supplier registration at RDSO.
• Application of statistical techniques for improvement of process or process capability studies.
• QAP Documentation & reports: Preparation of manuals for specifications and methods of analysis including process control samples for all products and packaging materials, and periodic updating as needed, maintaining records of all quality audits undertaken, Prepare documents as per country norms
• Preparation of Patent write-ups as per the requirement of Indian Patents Act, and co-ordination with Patent authorities.
• Customer Complaints: Root cause analysis of customer complaints, Making reports and resolution, Preparation of CAPA
• Attorneys/Examiners for patenting of developed oils/lubricants.
• Providing technical support including conducting Training programmes on Metalworking lubrication and Quality assurance of Machinery oils & Lubricants
• Development and Standardization of Testing /Analytical & In-house Calibration methods and arranging external calibrations thereof from time to time to ensure consistency, reliability, and accuracy of results.
• Laboratory Management, Maintenance of chemical laboratory
• Handled sophisticated analytical instruments like Spectrophotometers (Optical Emission, Infrared/FTIR, UV, AAS), Gas & Liquid Chromatography
• Familiar with oil testing methods including Automotive, Industrial, Solvents, sulphonates etc transformer oil testing
• Method development and validation, Proficiency Testing / Inter-laboratory testing, Calibration activities
• Preparing the Review and report compilations of analytical method development data and calibration reports.
• Taking appropriate quality measures including preparation / maintenance of necessary documents and conducting audits to ensure compliance with standards
• Interfaced with purchase and other departments for specific requirements.
• Collect & analyze data by statistical techniques for improvement of process or process capability studies

Preferred candidate profile

Perks and benefits