Supplier Quality Job Vacancies in Mumbai

Work Type: - Field Work Job Description:- The Quality Assurance (QA) & Quality Control vendor approval process involves evaluating a supplier's ability to consistently provide products or services that meet quality standards, including physical audits, sample analysis, and review of documentation. This process ensures that only reliable vendors are used to maintain product quality and safety, often a critical requirement in industries like pharmaceuticals. Here's a more detailed breakdown of the QA vendor approval process:1. Needs Assessment and Vendor Identification:Determine Needs: The organization identifies the need for a new vendor and the specific requirements for the product or service.Vendor Identification: Research and identify potential vendors who can meet the requirements. 2. Vendor Qualification:Vendor Questionnaire: Potential vendors are typically asked to complete a questionnaire that gathers information about their capabilities, quality systems, and compliance.Document Review: QA reviews the vendor's documentation, such as certificates of analysis (COAs), specifications, and method of analysis.Sample Analysis: The vendor provides samples, which are tested by Quality Control (QC) to ensure they meet the required standards.Site Audit: A physical audit of the vendor's manufacturing site is conducted to assess their quality control measures and overall compliance. 3. Vendor Evaluation and Approval:Compliance Assessment: A evaluates the results of sample analysis and the site audit to determine if the vendor meets the required standards. Risk Assessment: Vendors may be categorized by risk level, with those posing higher risks requiring more rigorous evaluation and monitoring. Approval Decision: Based on the evaluation, QA makes a decision to approve or reject the vendor. 4. Ongoing Monitoring and Re-evaluation:Performance Monitoring: Regularly monitor the vendor's performance on quality, timeliness.

Building and maintenance of quality standards as well as enforcing technical and testing standards. Monitoring of all the QA activities, test results, leaked defects, root cause analysis and identifying areas of improvement. Implement steps required to improve the processes. He must also be able to Inspect, test, or measure materials & Measure products with calipers, gauges, or micrometers.

IGNORE IF Already Applied .Required Qualification:1. M-Pharm or B-Pharm with Hands-on experience as QA Pharmacist in GMP / GDP environment2. Good Command over English.3. Mandatory to have Valid Pharmacy License and PPP.4. Experience : 5-10 years experience Mandatory*5. Age Limit : Up to 40 years1. Preparation, Revision & Training of QA SOP's:Hands on Experience of SOP ManagementPreparation & Revision of QA SOP's in Control Document Management System (CDM'S) as per requirement.To conduct Training of approved QA Sop's to all concerned persons.2. Audit & Inspection Readiness:Preparation of Annual Internal Audits schedule.Performing Internal Audits as per approved schedule.Preparation of Internal Audits report.Raised the CAPA's in Track-wise system after agreement with stakeholders.Verification of CAPA's effectivenessafter predefined period.3. Periodic Product Review:Preparation of Periodic Product Review (PPR) of the products.4. Preparation of Periodic Product Review (PPR) of the products.To support contract manufacturing sites for validations during product transfer.5. Process, Equipment, Facility & Utility Qualification:To permed change control assessment validation / qualification perspectives.Preparation and Maintenance of Site Validation Master Plan (SVMP).Preparation of Monthly presentation on Site validation Steering Committee.Tracking of monthly re qualification schedule.6.Cleaning Validation:Preparation of Cleaning Validation Protocols & Reports.Performing Clean Equipment Hold Time (CEHT) & Dirty Equipment Hold Time (DEHT) Study.7. Quality Management Systems:To carry out the gap analysis against Quality Management Systems.Handling change controls , deviations and CAPA's.Carry out risk assessment in view of change in process / introduction of new product.Raise and progress departmental change controls, deviations and CAPA'sJob Type: Full-timeSalary: 25,000.00 - 45,000.00 per monthBenefits:Hea

KEY RESPONSIBILITIES:-Analyze quality performance utilizing using statistical and analytical tools and methods.-Implement methods to inspect, test, and evaluate reliability, precision, reliability, and accuracy of processes, products, and production equipment.-Develop and establish quality procedures and systems for inspecting plans, quality trends, statistical plan price estimates and technical quality proposal plans.-Ensure process control documents adhere to set requirements.-Ensure on-time processing of non-conforming components.-Assist disposition process by involving in failure analysis and suggest corrective actions as Material Review Board member.-Coordinate with suppliers and customers relating to quality trends, performance, and corrective action.-Verify conformance and productivity of quality engineering system through supplier audits and surveys.-Initiate programs to enhance supplier performance.-Interact with product development committees to inspect and review engineering releases.-Review all product quality aspects like planning, manufacturing methods, and process specifications.-Interact with manufacturing and engineering teams to optimize documentation related to quality and inspection checks.-Report and supply subassemblies as well as finish goods following Device Master Record.-Interact with Quality Control Packaging team to conduct Technician Training Program after evaluating Quality Inspections Techniques.-Assist manufacturing scrap performance evaluation and management.