Female Quality Control Executive Jobs

We are looking for a Quality Assurance Executive with 5 to 10 years of experience in the pharmaceutical industry. The ideal candidate will ensure that all products meet quality standards and comply with regulations. **Key Responsibilities:**- **Quality Control Inspections:** Conduct regular inspections of products to ensure they meet established quality criteria and specifications.- **Documentation Review:** Verify all quality assurance documentation to ensure accuracy and compliance with industry standards.- **Process Improvement:** Identify areas for process enhancements and implement solutions to improve quality and efficiency in production.- **Compliance Checks:** Ensure that all operations comply with local and international quality regulations and standards relevant to the pharmaceutical industry.- **Training and Support:** Provide training and support to employees on quality assurance processes and best practices to foster a culture of quality.**Required Skills and Expectations:**The candidate must possess a B.Pharma or a relevant professional degree, with a strong understanding of quality assurance principles in the pharmaceutical field. Attention to detail and a methodical approach to tasks are essential. The ability to collaborate effectively with cross-functional teams and communicate clearly is crucial. Proficiency in quality management tools and methodologies is expected. Knowledge of regulatory standards governing the pharmaceutical industry will be beneficial. We are looking for a proactive individual who can work independently and make decisions that impact product quality positively.

Responsibilities:Inspection & Testing:Conduct thorough quality inspections of incoming raw materials, in-process components, and finished goods as per defined specifications, control plans, and sampling procedures.Perform various tests (e.g., dimensional checks, functional tests, visual inspections, destructive/non-destructive tests, as applicable to the product/industry) using appropriate measuring instruments and testing equipment.Operate and maintain quality testing instruments and equipment, ensuring their proper functionality and calibration status.Defect Identification & Reporting:Identify, document, and report any non-conformities, defects, or deviations from quality standards immediately.Segregate non-conforming materials/products and ensure proper tagging and disposition.Generate clear and concise inspection reports and test summaries.Documentation & Record Keeping:Maintain accurate and organized records of all quality inspections, test results, non-conformity reports, and corrective actions.Assist in preparing and updating quality documentation, including inspection checklists, standard operating procedures (SOPs) for quality processes, and quality control plans.Standard Adherence & Compliance:Ensure strict adherence to company quality policies, procedures, and relevant industry standards (e.g., basic understanding of ISO 9001 principles, product-specific standards like BIS, etc.).Monitor production processes to ensure that quality parameters are consistently met at various stages.Root Cause Analysis Support:Assist senior QA personnel or engineers in investigating the root causes of quality issues, customer complaints, and recurring defects.Support the implementation and verification of corrective and preventive actions (CAPA).Calibration Support:Support the periodic calibration of inspection and testing equipment, maintaining calibration records, and ensuring the availability of calibrated instruments.Feedback & Communication:Provide timely feedback on quality issues to the Production team, informing them of deviations and assisting in immediate rectification.Communicate effectively with supervisors, engineers, and other departmental personnel regarding quality matters.Continuous Improvement:Actively participate in quality improvement initiatives, such as 5S, Kaizen, and waste reduction efforts on the shop floor.Safety & Housekeeping:Adhere to all safety regulations and good housekeeping practices in the workplace, especially in testing and inspection areas.Local Communication:Communicate clearly and effectively with the production team, supervisors, and other colleagues. Fluency in Marathi and Hindi is essential for effective interaction on the shop floor. Good English proficiency is required for documentation and technical understanding.

Hiring employee for smart metering project in Distt GONDA , U.P . to check the Quality of old & New Meter online & Maintain the Excel sheets. to putup

Sampling and analysis of Raw materials, Packing materials and, In process, Intermediate and Finished products.Calibration of all QC instruments.Conducting Stability/Holding time studies.Handling of Reference Standards and qualification of Working Standards.Required Experience: 2-3 years experience in Pharmaceutical Quality ControlEducation Qualification : MTech /BTech Chemical /M.Sc. (Chemistry)/B.Sc. (Chemistry) Intergrated PG preferred

- Candidates should have good communication skill and team working spirit.Responsible for plant QA activities.- Responsible for release of raw, packing materials and finished products.- Responsible for compliance of Quality management system (QMS).- Responsible for review and approval of QMS, GMP and GLP documentations.- Responsible for review and approval of standard operating procedures (SOPs) of all the functions in the organization.- Responsible for online monitoring of production activities.- Responsible for Handling of change control, Deviations their impact assessment and closer and its tracking and follow up with concern for effective implementation.- Responsible for internal Audits and Customer Audits of the plant and their compliance.- Responsible for fill up Customer VQ documents and forward to them for their evaluation.- Review of Batch Manufacturing and Batch packing records and prepare Batch Release note.- Responsible for line clearance & In process checks, monitoring during manufacturing and packaging.- Execution of Hold time study for intermediate products and Establish Hold time period for the same.- Responsible for handling customer complaints.- Responsible for Vendor Qualification and Vendor Audits.

Location: Amritsar Company: Arneja Packaging IndiaJob Type: Full TimeSummary:-A quality checker/Supervisor assures that the items are safe and fulfil the manufacturer's specifications before they leave the factory or facility. They inspect each product to ensure uniformity and that buyers obtain a standard and suitable productExperience:-1 to 3 years of professional experience in quality assurance before they qualify for management positions. -Only Female candidates will be Preferred.-Must be a Gradate.- Should have basic knowledge of Computer, Ms word, Excel, Email, access to Internet.Responsibilities of Quality Control:-Read blueprints and Specifications.-Monitor Operations to ensure that they meet Production standards.-Recommend adjustments to the Assembly or Production Process.-Inspect, Test, or Measure Materials, Leakage, Scratch. -Measure products with Callipers, Gauges, or Micro meters.Basic quality tools-Check Parameters Dimension -Bernier-Google Sheet-Control chart To apply for this position, Please submit your resume and a cover letter detailing your relevant experience.Salary - Rs. 10,000 /-Sandeep Sharma HR ManagerArneja Packaging India *Arneja Packaging India Experts in manufacturing of plastic containers & closures since 1999. *Address: Arneja Packaging India, J 15/1450, New Baba Budha ji Colony, opp. New Amritsar Colony, Amritsar.

Prepared FSSAI required register and FileFSSAI form given below1. Potable Water Report 1510500.2. Food Material testing report.3. Incoming material specification and approved vendors.4. Time, Temperature, Logbook.5. Packaging material food grade.6. Recall.7. Cleaning Records.8. Preventive maintenance equipment & machinery AMC.9. Measuring & monitoring devices calibration, weight legal.10. Pest control-trained personnel, records.11. ETP/STP.12. Annual Medical Examination records.13. Training records FoSTaC.14. Internal external Audit records.15. Consumer complaints redressal. 16. Documents for appropriate period 1 year or shelf life

Wanted Female Chemist to work in Pharmaceutical manufacturing unit

Female PHARMACIST FOR MALDIVES1. Diploma/B. Pharm accepted2. TRANSCRIPTS Required.3. Experienced & Qualified in relevant field.4. Attractive Salary will be provided.

B.Sc./M.Sc. with 2 - 4 Years of relevant Experienced required in Pharmaceutical Company.