1062 Ipqa Jobs - Page 14

Walk-in Interview for Zydus Lifesciences Limited at Ahmedabad| 28th September 2025|Sunday We are recruiting for our Moriaya, Ahmedabad Unit . Walk-in Interview Details Interview Date : 28th September 2025 Interview Timings: 9:00 AM 4:00 PM Interview Location: Zydus Healthcare Ltd, Block 2, 3, 4, 5, Sigma Commerce Zone, Nr. Iskon Mandir BRTS Bus Stand, Ambli Bopal Road, Ahmedabad 380015. Job Location: Moraiya, Ahmedabad Education Qualification: ITI / Diploma / BE / B.Sc / M.Sc / B.Pharma / M.Pharma Experience: 2 – 8 Years Quality Assurance (IPQA) : Officer to Sr. Executive: IPQA in process (Mfg. & Pkg.) Engineering: Executive/Sr. Executive: Process Equipment (Mechanical/Electrical/Instrumenta...

About The Role : Job TitleTrading Enabler - VP LocationMumbai, India Role Description The candidate will be part of the Asset & Liability Management (ALM) function and responsible for reducing model risk associated with interest rate risk in the banking book (IRRBB) measurements. The team acts as an intermediary in treasury itself and between the business units and other central functions like Market Risk Management and Model Risk Management. This gives you a unique view into many exciting and important topics. Treasury Treasury at Deutsche Bank is responsible for sourcing, managing, and optimizing Deutsche Bank's financial resources and providing high-quality steering to the Bank on financi...

Responsibilities: Conduct process validation studies Ensure compliance with regulatory requirements Manage vendor qualifications Lead cleaning validation processes Oversee IPQA activities Flexi working

Role & responsibilities Responsible for Batch release Responsible for ERP Approvals. Verification of Instrument/Equipment log books for their online entries Deliver the responsibilities assigned by HOD / designee. Review of calibration of analytical instruments and equipment. Review of audit trails and participation in internal Audits. Review of IQ, OQ, PQ of Analytical instruments and equipment. Review of volumetric Solutions, Reagents and Buffers preparation records. Responsible for review the failure investigation reports of root cause analysis. Responsible for Handling of QMS elements through Agile PLM system Responsible for cleaning verification and line clearance of dispensing booths l...

We are looking for a detail-oriented QA to ensure the delivery of high-quality products, services, or processes. The QA will be responsible for evaluating performance, Areas for improvement & ensuring compliance with internal and client expectations. Required Candidate profile GMP BOM Quality assurance BMR

1 Responsible for the Handling of market complaint at site. 2 Responsible for the Handling of Deviation management at site. 3 Responsible for the Handling of CAPA and Global CAPA management and effectiveness checking at site. 4 Responsible to co-ordinate the execution of mock recall and market recall. 5 Responsible to review and tracking of Audit Responses. 6 Responsible to raise, review and tracking of Quality Alert. 7 Responsible to ensure timely closure of QMS documents. 8 To perform activity as per authorization in EDMS, LMS and TRACKWISE software. 9 Responsible for performing IPQA activities. 10 To perform process validation and cleaning validation sampling activity in shop floor. 11 To...

About The Role Job Title - Internal Audit Analyst Management Level :11 Analyst Location:Bangalore Must have skills: Chartered Accountant with 2 - 3 years of post-qualification experience in external or internal auditing, preferably in Big 4 or a global organization. Good to have skills: Internal Audit experience with Big 4 or a global organization Job Summary : An agile, highly motivated, innovative thinker with a background in audit, risk, or compliance looking to join a fast-paced, global Internal Audit department that has embraced transformative capabilities including advanced analytics, dynamic risk assessment, and automation to retain its role as a trusted advisor to the business. You a...

To ensure and carry out the analysis of stability sample and all other activities as per Standard Operating Procedure (SOP). To get involve and support in investigation of failure of any material or product in case of any out of specification (OOS) or Out of trend (OOT) or laboratory incident or non-conformity and take corrective and preventive actions. To raise and implement change control or document change request wherever necessary. To follow and ensure Good Laboratory Practices (GLP), Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) inside Stability lab. To ensure availability of the working & impurities standards as per various pharmacopoeia. To assist Supervis...

QA role in API manufacturing. Responsibilities: Documentation, internal/vendor/regulatory audits (USFDA, WHO, EU), deviation handling, validation, CAPA, QMS compliance, and conducting training to promote quality culture. Office cab/shuttle Provident fund

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

Roles and Responsibilities Ensure compliance with cGMP guidelines during line clearance activities. Conduct BMR reviews, BPR reviews, and stability analysis reports. Review SOPs, protocols, and reports related to quality assurance. Perform material release and batch release tasks. Verify documents such as BMR, BPR, Stability Analysis Report, etc.

Role Overview: As a Team Member in IPQA for Injectables/OSD, you will be a skilled professional with over 5 years of experience in real-time monitoring of manufacturing and packaging processes. Your responsibilities will include line clearance, in-process checks, and reviewing Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) to ensure compliance with GMP and regulatory standards. You will also be involved in deviation handling, documentation, and providing audit support for injectable and oral solid dosage forms. Key Responsibilities: - Real-time monitoring of manufacturing and packaging processes - Conducting line clearance and in-process checks - Reviewing Batch Manufactur...

To carry out IPQC/IPQA during the manufacturing stages. To conduct various LAB TEST as and when required. To give proper reports of TEST to Higher Authorities as and when asked. To prepare/maintain reports of QA department as per ISO guidelines.

About Company Founded in 2011, ReNew, is one of the largest renewable energy companies globally, with a leadership position in India. Listed on Nasdaq under the ticker RNW, ReNew develops, builds, owns, and operates utility-scale wind energy projects, utility-scale solar energy projects, utility-scale firm power projects, and distributed solar energy projects. In addition to being a major independent power producer in India, ReNew is evolving to become an end-to-end decarbonization partner providing solutions in a just and inclusive manner in the areas of clean energy, green hydrogen, value-added energy offerings through digitalisation, storage, and carbon markets that increasingly are integ...

Role & responsibilities To ensure GMP practices are followed during various stages of production activities of finished drug product. To perform in process checks in Tablets/Capsule/Ointment/ Liquid/Dry powder To ensure various operations are complying as per SOP. Daily & Monthly calibration of IPQC instruments. Sampling of Control and Stability samples. To ensure that the facility is maintained in a clean and sanitary conditions. In-process checks during dispensing & secondary packing activities. To ensure timely sampling of finished products, control samples, validation samples & stability samples. To monitor Dispensing of raw material and packing material required for the manufacturing of...

Role & responsibilities Exciting opportunity for IPQA Executive at our USFDA approved OSD Manufacturing facility Company : Apothecon Pharmaceuticals Pvt Ltd Website : www.apotheconpharma.com Location : Vadodara Experience : 4 - 9 Years Dept. & Sub Dept. : QA - IPQA - OSD MFG Designation : Executives 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. Preferred candidate profile Dynamic work environment Career development opportunities Work-life balance Free transportation Canteen facility Free insurance cover...

Preferred candidate profile Candidate must be from API/Bulk Drugs/ Chemical Industry. Role & responsibilities Quality System Management: Develop, implement, and maintain quality assurance policies and procedures in line with cGMP, ISO, and other relevant regulatory standards. Team Leadership & Mentoring: Lead, manage, and train the QA team, fostering a culture of quality and continuous improvement. Process & Product Quality: Oversee quality testing activities, analyze quality trends, identify non-conformities, and ensure the final API product meets high-quality standards. Supplier Quality Management: Provide Quality oversight of external vendors, assess supplier qualifications, and manage AP...

Develop and implement a strategic vision for the QA function aligned with the company's overall business goals. Provide leadership and direction to the QA team, ensuring a consistent and integrated approach to quality management. Develop, implement, manage, audit and maintain GMP quality systems. Coordinate and perform all vendor qualification and compliance Should have well versed with handling of Regulatory Audits, APQR, OOS, OOT, Investigation, Laboratory Compliances, HVAC & Water Qualification & Validation, IPQA, Lab QA, Validation & Qualification and QMS. Develop, manage and maintain a GMP compliant document control system. Oversee investigations of all non-conformances (deviations, err...

Role & responsibilities (1) To perform the daily IPQA related activity and line clearance related activity.. (2) To monitor the plant critical areas like clean room (Manufacturing / Filling), Packing, labelling, OBD verification, water system, utility supply area etc. for the GMP compliance. (3) To ensure the End to End Control in Manufacturing, packing and material storage activity (4) To prepare and review GMP documents such as SOPs, protocol and other relevant documents. (5) To review the executed batch manufacturing / packing records and review of COA & analytical data. (6) Handling of Control sample management and review of stability sample management procedure and its compliance. (7) T...

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.

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities Injectable Manufacturing (Executive/Senior Officer / Officer) Experience - 02 to 08 Years Qualification - B. Pharmacy/ M Pharmacy / Msc / Bsc / Engineering - (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification BE / B Tech QUALITY ASSURANCE IPQA (injectable) / QMS / Documentation (Officer / Senior Officer /...

Dishman Group 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 personnel and implementing th...

Role & responsibilities Quality Control: Perform High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), and various wet chemical analyses to ensure product quality. Analyze raw materials, intermediates, and finished products as per established quality standards. Prepare SOPs in line with regulatory requirements, including stability studies and market sample analysis. Ensure GLP-oriented documentation and maintain accurate records for audits and compliance. Work proficiently on multiple laboratory software platforms to support analytical testing and reporting. Quality Assurance: Ensure cGMP and regulatory compliance across all QA operations. Manage AQA, IPQA, batch release, d...

Roles and Responsibilities For IPQA BMR review. To ensure the line clearance to the production unit. To ensure all QA activities are carried out as per the Standard operating procedure. Issuance, Retrieval, Approval & Controlling of all Quality related Documents (i.e. CSOP, SOP, STP, GTP, Protocol, etc.) Preparation, Review, and Retrieval of SOP. Candidate must have relevant experience in IPQA API Industries. Should have good communication and interpersonal skills. For QMS Direct involvement in Deviation and Process Investigation. Handling of Change Control, Process Validation, Qualification, APQR, and Trend Report. Handling Market Complaints, Audit Compliance Reports & QMS-related activitie...

Works independenly on creating test plans, executing tests, troubleshooting the issues, automating test cases, reporting bugs with all the required details, reviewing the tests, providing the test reports, analyzing test failures Capable of analyzing moderately complex challenges using analytical tools and data interpretation. Applies critical thinking to assess problems with relevant data independently to evaluate potential solutions after considering various possibilities. Engages in independent analysis and collaborates with others to gather insights and develop recommendations including challenging existing processes. Capable of working independently while actively contributing to team a...