1072 Ipqa Jobs - Page 43

Roles and Responsibilities Conduct quality audits, inspections, and IPQA activities to ensure compliance with GMP regulations. Perform BMR reviews, CAPAs implementation, and participate in process validation activities. Ensure timely completion of documentation related to quality control processes. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Maintain accurate records of all quality-related documents and reports. Desired Candidate Profile 1-2 years of experience in Quality Assurance/Quality Control or Regulatory Affairs department. Bachelor's degree in Chemistry (B.Sc) or Dairy Technology (B.Tech). Strong understanding of Good Manufactur...

Reporting To Service Manager Job Description Onsite Customer visit for Installation & Support to resolve all technical issues Coordination with technical/software team for removing Bugs Coordination with sales and coordination team for all supply issues Resolve all the technical & non technical issue onsite. Provide solution to software/hardware issue in consultation with Software / Embedded / CCD team Discussion with customer and resolve all issues Preparation of Service Reports and Issue wise MOM Completion of RMA in coordination with CCD, Sales & Dispatch for proper handling of returnable and non-returnable material Regular training program at customer end in order to educate regarding Je...

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

Job Receiving user indents, verifying with approved budget, and floating RFQ to the vendor (minimum 2 to 3 vendors). Preparing a worksheet to validate supplier quotes based on cost, quality, OEM, and delivery lead time Knowledge of SAP for PO release. Create PSR and follow the PSR approvals stage-wise. PO release. Monitoring material delivery against committed vendor dates. Coordinating with the maintenance team for installation and commissioning. Coordinating with the logistics team. Coordinating material in warding and acceptance, and vendor payment. Asset management and handling the Audits Generating and circulating reports to management. Relevant Experience: Mechanical and Electrical, Co...

As a Solution Tester, you will be responsible for: 1. Designing and automating test suites to ensure reliability of the system z(s390x) platform technology 2. Having a client-first mindset to test at scale and imitate customer-like environments 3. Creating strategies and scripts to test new features and functionalities 4. Contributing and reviewing code for internal and external repositories 5. Documenting processes (Test plans) and procedures for clarity and reproducibility 6. Interacting with counterparts in US/Germany teams and Red Hat Required education Bachelor's Degree Required technical and professional expertise Required Technical and Professional Expertise with relevant experience o...

Novo Nordisk Global Business Services (GBS) India Department: GCM DP RoW Location Hyderabad, India Are you an experienced aseptic manufacturing project manager with a strong technical background and a passion for making a direct impact on patients'' livesDo you thrive in an international environment where cultural awareness is key to your successIf so, this could be your dream role! ApplyNow! The Position As a Project Manager in Aseptic Manufacturing, you will lead and mentor cross-functional teams, including both Novo Nordisk and our Contract Manufacturing Organisation (CMO) partners. It includes, Ensure the seamless Technology Transfer and manufacturing of our commercial products, always u...

Novo Nordisk Global Business Services (GBS) India Department GCM DP RoW Job Location Hyderabad Are you an expert in aseptic manufacturing with a strong quality mindset and a desire to make a tangible impact on global healthNovo Nordisk is seeking a dedicated Manufacturing Specialist to join our Global Contract Manufacturing Drug Product (GCM DP) team in Hyderabad, India. In this role, you''ll be crucial in ensuring the high-quality production of life-saving insulin and GLP-1 products through our Contract Manufacturing Organizations (CMOs). ! The Position As a Manufacturing Specialist (SME), you''ll be the go-to expert driving Technology Transfer projects for commercial products, ensuring top...

JD: 1) To be prepared document related to audit as per audit agenda. 2) Filled vendor questionnaires & prepared related documents. 3) Keeping record of key Customer. 4) To be prepared process validation protocol and report as per seniors guidance. 5) To be prepare cleaning validation protocol and report as per seniors guidance. 7) To be prepared master, controlled, uncontrolled, reference, obsolete & distribute documents as per SOPs and formats requirement. 8) To help the senior for preparation of CAPA according to audit report. 9) Issuance of Change control, OOS, deviation & other QMS formats whenever required from respective department and retained record in logbook. 10) To be prepared BPC...

Responsibilities: Participate in management review meetings. Review of department trend analysis reports and internal studies or investigations. Ensure corrective action is initiated when required. Provide complete analysis of test results, investigation or information studies. Be capable of assuming study director responsibilities for all routine testing as well as certain advanced or specialized studies as requested by clients. Duties may include test scheduling, test preparation, proper application of test method(s), data collection, data review, and approval of final report of analysis. Maintain thorough knowledge and understanding of all SOPs pertaining to microbiology/sterility assuran...

Responsibilities: Preparation, Review and Issuance of Departmental Sops, Guidelines and Policies. LNB's and Logbooks Issuance and Checking for daily entries in Logbooks. To Review various Documents like Change controls, Incident Reports, CAPA, OOS Results, Deviations, Issuance Records and Internal Audit Reports. Prepare, Review and Maintain Qualification Documents, Review Instrument Calibration Reports QMS activities Training of New Employees, Preparation of Job Description, maintaining Training Files. Issuance of various documents like LNBS, Logbooks, Formats, Register, Sops, Lists, Job Descriptions etc. Allocation of Equipments /Instrument Numbers, Product and employees Code, Register and ...

Urgently hiring for IPQA Assist. Engineer - Offroll Company Name - EMS Manufacturing - Payroll - Adecco Address - Oragadam, Chennai, Tamil Nadu Position Title - IPQA Assist. Engineer Department - In process Quality Salary 20 K to 25 K + PF + Food +Transport Key Responsibilities: Prepare, update, and maintain Work Instructions, FPI/FAR reports, and other line documentation. Monitor line yield, participate in daily reviews, and work with CFT to implement corrective and preventive actions. Prepare FMEA and Control Plans to identify and mitigate risks. Conduct process and ESD audits to ensure adherence to QMS and product requirements. Manage quality control at various stages, including special p...

Urgently hiring for IPQA Assist. Engineer - Offroll Company Name - EMS Manufacturing - Payroll - Adecco Address - Oragadam, Chennai, Tamil Nadu Position Title - IPQA Assist. Engineer Department - In process Quality Salary 20 K to 25 K + PF + Food +Transport Key Responsibilities: Prepare, update, and maintain Work Instructions, FPI/FAR reports, and other line documentation. Monitor line yield, participate in daily reviews, and work with CFT to implement corrective and preventive actions. Prepare FMEA and Control Plans to identify and mitigate risks. Conduct process and ESD audits to ensure adherence to QMS and product requirements. Manage quality control at various stages, including special p...

KRA: Develop, implement, monitor QC procedures Inspect products at various stages of production Analyze data to identify areas for improvement Handle customer complaints, Customer/ ISO/ 3rd party audits Supplier quality management Root cause analysis Required Candidate profile Degree/ Diploma/ PG Diploma in mechanical 5+ years' experience in quality in technical textiles/ abrasives/ auto component industry Ready to travel or relocate to Murbad, Kalyan, MH

Corona Remedies Pvt. Ltd., is looking for Sr. Executive to join our dynamic team and embark on a rewarding career journey Leading the full audit cycle by checking tax compliance, verifying financial records, and inspecting accounts. Analyzing the results of the audit and presenting possible solutions for ineffective financial practices to management. Evaluating company accounting procedures, payroll, inventory, and tax statements to guide financial policymaking. Conducting risk assessments to recommend aversion measures and cost savings. Following up with management to ensure remediations are implemented into the company's financial practices. Supervising junior auditing personnel and implem...

Infinite Computer Solutions India Pvt. Ltd. is looking for Senior Executive to join our dynamic team and embark on a rewarding career journey Leading the full audit cycle by checking tax compliance, verifying financial records, and inspecting accounts. Analyzing the results of the audit and presenting possible solutions for ineffective financial practices to management. Evaluating company accounting procedures, payroll, inventory, and tax statements to guide financial policymaking. Conducting risk assessments to recommend aversion measures and cost savings. Following up with management to ensure remediations are implemented into the company's financial practices. Supervising junior auditing ...

Job Responsibilities: To ensure implementation of cGMP norms in manufacturing areas To give line clearance in dispensing, manufacturing and packaging To monitor dispensing, manufacturing and packaging Sampling of In-process, finished stage and process validation batches and forwarding the same to Quality Control department for analysis To ensure that gowning and entry/ exit procedures are followed as per standard procedures Monitoring of environmental conditions (temperature, humidity & pressure differential) in manufacturing areas To carry out IPQA checks in manufacturing and packaging areas To ensure online documentation To verify that the appropriate qualification, calibration and prevent...

Senior QA Executive (OSD plant experience preferred, first priority). Experience: 5 To 7 years in QA, with minimum 1 years in managerial role. Education Qualification: B.Pharm | M.Pharm | M.Sc. Department: Quality Assurance. Location: Santej Ahmedabad. Industry: Pharmaceutical. Facilities Provided: Transportation Facility Available (As Per Circumference Of Sunrise Remedies)* Mediclaim and Food Facility provide By Company.* Key Responsibilities: Strong knowledge of IPQA, documentation control, and QMS. Good understanding of WHO-GMP, cGMP, and international regulatory requirements. Excellent problem-solving, and decision-making skills. Good communication and leadership skills. Allocate respons...

Qualification: Post-graduate in Pharmacy or Pharmaceutical Engineering Experience: 15 to 20 years in sterile manufacturing plant operations, with a minimum of 10 years in a leadership role and at least 7 years in a regulated sterile manufacturing environment. About The Company Fresenius Kabi Oncology Limited, a wholly owned subsidiary of Fresenius Kabi, is a leading player in the oncology generics market with a broad portfolio that includes injectables, cytotoxic, and APIs. Its state-of-the-art production facility in Baddi features dedicated units for cytotoxic and non-cytotoxic products, including liquid and lyophilized injectables. The facility is approved by global regulatory authorities ...

Infinite Computer Solutions India Pvt. Ltd. is looking for Senior Executive to join our dynamic team and embark on a rewarding career journey Leading the full audit cycle by checking tax compliance, verifying financial records, and inspecting accounts. Analyzing the results of the audit and presenting possible solutions for ineffective financial practices to management. Evaluating company accounting procedures, payroll, inventory, and tax statements to guide financial policymaking. Conducting risk assessments to recommend aversion measures and cost savings. Following up with management to ensure remediations are implemented into the company's financial practices. Supervising junior auditing ...

1.To Initiation , review and conduct Calibration of IPQA Instruments. 2.To review all usage logs of Manufacturing and Packing Area. 3.To review and follow up for Annual Maintenance Activity of IPQA Instruments. 4.To fill and review IPQA instruments log books. 5.To review and provide Line Clearance for Manufacturing Equipments / Packing Equipments.

Handling of Manufacturing Compliance i.e. IPQA Activity Handling of QMS Documents like CAPA, and OOS and Change control Handling of APQR Handling of Batch release activity Good in communication skills Exposure of audit

Aster Medcity is looking for Senior Executive.Information Technology.MIMS Hospital Kottakkal to join our dynamic team and embark on a rewarding career journey Leading the full audit cycle by checking tax compliance, verifying financial records, and inspecting accounts. Analyzing the results of the audit and presenting possible solutions for ineffective financial practices to management. Evaluating company accounting procedures, payroll, inventory, and tax statements to guide financial policymaking. Conducting risk assessments to recommend aversion measures and cost savings. Following up with management to ensure remediations are implemented into the company's financial practices. Supervising...