1072 Ipqa Jobs - Page 42

Job Area: Finance & Accounting Group, Finance & Accounting Group > Internal Audit General Summary: Job Overview Qualcomm is a company of inventors that unlocked 5G - ushering in an age of rapid acceleration in connectivity and new possibilities that will transform industries, create jobs, and enrich lives. But this is just the beginning. It takes inventive minds with diverse skills, backgrounds, and cultures to transform 5Gs potential into world-changing technologies and products. This is the Invention Age - and this is where you come in. This is a unique opportunity to join Qualcomm"™s finance and accounting organization based in Hyderabad in the Corporate Internal Audit & Advisory Services...

QA & QC Executive Job Description Position Overview The QA & QC Executive is responsible for ensuring that products meet quality standards and regulatory requirements through systematic inspections, testing, and process monitoring. This role involves collaboration with production teams to implement corrective actions and continuous improvement initiatives. Key Responsibilities Quality Control & Inspection Conduct inspections on raw materials, in-process products, and finished goods to identify defects or deviations from quality standards. Utilize measurement tools and testing instruments to verify dimensions and other quality criteria. Monitor all operations that affect quality and report ma...

Role & responsibilities Conduct in-process checks during various stages of sterile injectable manufacturing, including dispensing, compounding, filtration, filling, and sealing. Perform line clearance and area clearance before the start of manufacturing and packaging operations. Monitor aseptic practices and personnel hygiene compliance inside cleanrooms and controlled areas. Verify critical process parameters and environmental conditions during batch processing. Ensure compliance with SOPs, batch manufacturing records (BMR), and batch packaging records (BPR). Participate in visual inspection activities and oversee container-closure integrity checks. Monitor the usage and replacement of ster...

Handling of Day -to -Day activities of IPQA Handling of Market Complaints along with preparation /review of Investigation Reports for the same and prepare MIS for the same. Actively participate in MOH & client Audit as a runner, scriber, explainer

Exciting opportunity for IPQA Executive at our EU approved OSD Manufacturing faculity (UNIT 1) @ Moraiya, Ahmedabad!! Company : Unison Pharmaceuticals Pvt Ltd Website : www.unisonpharmaceuticals.com Location : UNIT 1 , Moraiya, Ahmedabad Experience : 4 - 9 Years Dept. & Sub Dept. : QA - IPQA - OSD MFG Designation : Executive Job description (Not limited to): Collect in-process and Finished sample as per Specifications and Protocol. Check documents like equipment log books, temperature & humidity records. Line clearance of machine & manufacturing area . Checking of batch manufacturing record. Perks & Benefits Dynamic work environment Career development opportunities Work-life balance Free tra...

Position : Section Head - Batch Release QA Functional Area: QA Reports to: QA Head Grade: G9B Department: Quality Location: Halol (OSD) POSITION SUMMARY Responsible for IPQA activity and strategy in line with Sun Pharma Compliance, Product Quality Management objectives and Regulatory requirements. Responsible for planning and arranging for internal and external departmental support of quality assurance activities as directed in approved protocols, quality systems or Procedures. Identify and implement solution for improving existing site quality assurance systems and processes Involvement in co-ordination of activities for software like SAP HANA at plant Responsible for review and Approval of...

Position: IPQA OFFICER Education: BSc. in chemistry, MSc. in chemistry or B.pharma / M.Pharma Experience: minimum 10 year in API pharmaceutical industries. Salary: 50 to 70 K per month Mo No : +91 90816 99400 / +91 90816 88100 / 90816 99600 Required Candidate profile Coordinate with regulatory authorities for inspections, licensing, and compliance documentation. Investigate quality incidents, deviations, and complaints, ensuring timely resolutions

Seeking a IPQA Executive to ensure skincare products meet regulatory, safety, and quality standards. Work closely with manufacturing, R&D, and QC teams. Requirement: 2+ years of QA experience, preferably in cosmetics or pharma manufacturing. Required Candidate profile Skincare manufacturing & QC expertise Knowledge of FDA, GMP, ISO regulations Attention to detail & procedural compliance Strong analytical, problem-solving & com skills Ability to work with GMP proces

Core Responsibilities: o Download data from Systems and mapping the same as per the requirement, co-ordinating with different teams for the data and checking its accuracy o Preparing Daily, Weekly & Monthly MIS reports o Preparing presentations,dash board, Graphs and analytical reports o Co-ordinating with the branches for feedback and any query related to customer handling. Support the manager in rolling out the new projects and initiatives and also updating on the progress and its impacts Desired Experience: Minimum 0-3 years in the field. Graduate : Yes Masters/Postgraduate: Optional Location - mumbai,delhi,pune,bangalore,hyderabad,chennai

Set up and operate blister packing machines, Load materials, Monitor line performance & adjust settings as needed. Inspect packs, complete logs, checklists, and deviation reports.

Job Description Preparation & Review of SOP’s of QA system and review / approval of SOP’s of other departments. Review of master BMR/BPR of commercial and exhibit batches. Review of BMR / BPR, scale-up and placebo batches. Review of executed BMR/BPR of commercial and exhibit batches for batch release. Issuance, Retrieval & Destruction of SOP’s, STP, specification, BMR/BPR, annexures & other formats. Login and review of quality system documents such as Deviation and IPOOS. In-process Quality Assurance during Production / Packing activities. Sampling at different stages of manufacturing / packing as per the requirement (In-process, BU, CU, finished, control, QP, Hold Time & stability etc.) Rev...

Tool Box Meeting Conducting daily toolbox meeting befor the shift starts Timeliness , No.of meetings conducted Manpower Allocation Allocating contract manpower in such a way that they would generate productivity of more than 60 MT/ group Standard v/s Actual Productivity Shift management Ensure loading & stabilization of material as per SOP SOP v/s Actual Reporting of breakages,cullet& not found material during the shift No.of times stock not updated Ensuring loading of correct material in truck as per Loading slip No.of Trucks wrong loaded Avoiding loose box generation in warehouse by closely monitoring the loading point & warehouse to reduce breakages No of breakages due to loose box Collec...

Key Responsibilities: Assist in developing and implementing quality assurance policies, procedures, and standards. Oversee day-to-day QA operations to ensure compliance with internal and external quality standards. Lead and mentor the QA team to enhance skills and ensure productivity. Conduct audits and inspections of processes, products, and documentation to identify non-conformances. Analyze quality data and prepare reports for management review. Collaborate with production, R&D, and other departments to address quality issues and implement corrective actions. Manage customer complaints related to quality and ensure timely resolution. Participate in the selection, validation, and qualifica...

Safety Management SystemOf Manpower:- To follow SOP's for safety so as to build safe working environment in shift. No. of First aid cases/nearmiss. No. of time PPE not used by subordinates. No. of time PTW system not followed.Operation & Schedule Management To follow the Operation scheduled activities in order to provide & to ensure smooth operation of equipment & machine. No. of instance motor changeover schedule not followed. No. of instance of utilities failure. No. of times Reading not taken as per schedule. Report generation of Daily utilities consumption. No. of times Report is not generated on time.Daily routine Patrol checking as per schedule.No. of instance patrol checking not done ...

Department: Quality AssuranceReporting To: Quality Assurance Manager / Head of QualityJob Summary: We are seeking a diligent and detail-oriented Deputy Manager Quality Assurance to join our team. The ideal candidate will support the QA Manager in ensuring that products, processes, and services meet the highest quality standards and comply with regulatory requirements. You will play a key role in developing, implementing, and monitoring quality assurance processes to drive continuous improvement. Key Responsibilities: Assist in designing, implementing, and maintaining quality assurance policies, procedures, and standards aligned with company and industry best practices. Lead and coordinate qu...

Department: Quality AssuranceReporting To: Quality Assurance Manager / Team LeadJob Summary: We are looking for a detail-oriented and proactive Senior Executive Quality Assurance to ensure our products and processes consistently meet quality standards. The role involves conducting inspections, supporting quality control processes, identifying defects, and assisting in continuous improvement initiatives. Key Responsibilities: Perform quality inspections and tests to ensure products and processes meet defined standards. Monitor production processes for compliance with quality specifications and identify areas for improvement. Document and report non-conformities and assist in root cause analys...

Office Administration HO Asset Tracking, asset allocation and Records1) 0 Gap 2) No Policy Violation 3) No Customer GrievanceCheck all AIS Admin on-line portals as a checker and escalate deviations to Sr Executive Admin1) No Gap 2) Maximum 1 working day to escalate gapsBooking of Hotels, Guest House, Taxi for outstation employees, expats etc1) 0 Gap 2) No Policy Violation 3) No Customer GrievanceVehicle Fuel, R&M and Trackers1) 0 Grievance 2) No SOP violation 3) Within budgeted costMISAll Corp Admin MIS except MIS handled by Unit Head Admin for specific office1) Maximum 3 working days gap to updatation 2) No Policy Violation Location Issue Logs- Plan, execute, Record and share MoM1) No Gap 2...

Develop thorough test plans and document the results and progress Develop in-depth functionality and stability automatic tests that will map customer use cases Research the right set of workloads and benchmarks Develop automated test scenarios and environments for End2End automatic evaluation Collect test evidence measurements to ensure system functionality, stability and scalability Establish automatic measures to assess the accuracy Analyze results to find ways to improve functionality coverage Analyze root causes and identify areas for improvement Collaborate with development teams to drive resolution for issues and improvement Generate test automation summary reports for stakeholders rev...

Job Description QA-Qualification Injectable /Parenteral (Officer/Senior Officer/ Executive) Job Location Sanand, Ahmedabad (Injectable Facility) No of Position - 03 Total Experience - 2-7 Years in Injectable Manufacturing Education B. Pharmacy/M. Pharmacy Will appreciate immediate joiner for this role Oversight and Governance QA ensures that all qualification activities (DQ, IQ, OQ, PQ) follow Good Manufacturing Practices (GMP) and regulatory guidelines (e.g., US FDA, EU GMP, WHO). Participates in project planning for qualification activities. Reviews and approves Qualification Master Plan (QMP). Document Review and Approval: QA is responsible for reviewing and approving all qualification do...

Set up bolus compression machines acc. to production specifications, Adjust machine settings, Identify & report mechanical issue, Load raw materials (powder/granules) into the machine hoppers, Maintain accurate production logs.

Vibonum Technologies Private Limited conducting a Walk-in interview in Quality Assurance department for its OSD Plant at Nanjangud, Mysore. Kindly carry your, latest 3 Months salary slip, appointment letter with CTC breakup and previous company relieving letters. ----------------------------------------------------------------------------------------------------------- Open vacancies in Quality Assurance for: IPQA Manufacturing : Exe > 08-10 Yrs IPQA Packing & Warehouse : Exp > 8 - 16 Yrs QMS: Exe / Sr. Exe : Exp > 08-10 Yrs CSV / ITQA/ Electronic DI compliance : Exp > 10-12 Yrs Process Validation : Exp > 08-10 Yrs AQA / Lab QA : Exp > 08-10 Yrs Documentation Cell : Exp > 04-08 Yrs AM/DM/Man...

Post- Junior Engineer Quality Assurance Email - jobpune12@gmail.com Contact - 9356395439 Experience - 04-08 yrs Edu - DME / BE Mechanical Location - Pune Pirangut Industry - Automotive JD Conduct in-process inspection of machined parts Manufacturing QA to ensure in-process quality, maintain compliance . Maintain IATF 16949, ISO 9001 & PPAP documentation and support audits. Prepare PDIR, 8D/RCA methodology QC tools, gauges, control plans, PPAP, ERP, and machining component Handle customer quality interactions .

Documentation Management Creation, revision, upgradation, and review of SOPs, protocols, and reports. ERP Management – Updating, modifying, and approving ERP entries for QA processes. Validation & Qualification – Execution and review of validation and qualification activities. Calibration & Mapping – Ensuring timely calibration and mapping of instruments and equipment. Quality Management System (QMS) – Handling deviations, investigations, CAPA, and change control. In-Process Quality Assurance (IPQA) – Performing line clearance, sampling, and dispensing checks. Audit Management – Planning, execution, and ensuring compliance for internal and external audits. Sample Management – Stability and r...

Opening for Pharma company Location : Mahemdabad Role & responsibilities : Continuous process Monitoring Batch Release of Finished product Collection of Sample ie in-process, Finished Product , Control, Stability and Tendor Knowledge of Collection of Validation samples i.e process validation, cleaning and hold time validation. Knowledge of review of Master and executed MFR/BMR and MPR/BPR Adequate knowledge of Inprocess checks of Tablet ,Capsule ,Liquid and Ointment. Adequate knowledge of Shop floor related Non-compliance ,its root cause and compliance. Adequate knowledge of calibration of instruments ie weighing balance , friabilator, DT apparatus, hardness tester, Vernier calliper, Moistur...

Interview For QA & QC Department for MNC Formulation Company in Navsari Qualification : Bsc / Msc Chemistry/ B.pharma/M.Pharma Experience : 3 to 8 Years CTC : Up to 8 LPA Send CV on sdpbharuch@gmail.com with Subject: Navsari QA & QC Navsari