1062 Ipqa Jobs - Page 18

Role & responsibilities Ensure compliance with cGMP, regulatory, and internal quality standards. Manage QMS activities deviations, change controls, CAPA, OOS/OOT, document control, etc. Handle Analytical Quality Assurance (AQA) activities data review, audit readiness, and compliance monitoring. Oversee In-process Quality Assurance (IPQA) – batch manufacturing records review, shop floor monitoring, line clearance, process compliance. Conduct internal audits, support external audits (regulatory and customer), and ensure timely closure of audit observations. Drive new initiatives in digitalization, automation, and process improvement in QA systems. Training and mentoring of team members to stre...

Job Descriptions ( Papier Creations, Bangalore Role : JOB DESCRIPTION QA QC Execuitve 1. Production Area Testing of all new supplier samples before finalising (inhouse) In case inhouse facility not available, sent for external testing and analyse Prepare the complete files for application of new licenses to the department Ask for COA and relevant reports from all suppliers Do spot checks for Finished Goods in hand 2 . Finished Goods tests Check for the quality of each batch before material is handed over for dispatch Maintain Quality Control Samples for the expiry period (2 packs per batch) 3 Records Maintenance Sales, Purchase, Expense files, E way bills, Debit Notes etc Purchase Orders, Pr...

Role Purpose 1) Support all documentation and regulatory requirements for international markets 2) Application management with FDA for license 3) Co-ordinate for Export Orders 4) Technical support for Plant / IPQC Key Responsibilities 1) Product Registration and Company Registration in International Market 2) Applications for domestic & Export licenses to FDA 3) Co-ordination for Export orders 4) Support plant with technical information when needed Key Activities 1) Documentation for application filing for licenses to FDA 2) Work with FDA/CDSCO as required during the filing of paper work for licenses, etc. 3) Art work approvals 4) Finalizing export orders with regards to packing, packaging m...

As a Production Area Handling Specialist, you will be responsible for overseeing the manufacturing processes of tablets and capsules. This includes ensuring smooth operations, monitoring equipment performance, and maintaining quality standards. Your duties will also involve the preparation and filing of Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) in compliance with regulatory guidelines. Attention to detail and accuracy are crucial in this aspect of the role. In addition, you will be tasked with managing the manpower within the production area, ensuring optimal utilization of resources and manpower efficiency. Effective communication and leadership skills will be essent...

As an Assistant Manager in the Contracts_WMEL team, you will be responsible for managing and overseeing all aspects of contract administration within the organization. This includes but is not limited to drafting, reviewing, and negotiating contracts, ensuring compliance with labor laws and statutory requirements, and managing relationships with stakeholders. You will also be responsible for preparing and maintaining all necessary documentation and reports related to contracts.

Role & responsibilities To supervise all IPQA/QMS function activity on daily basis and update to Section Manager. To conduct and participate in CAPA meetings and review summary report of the same within defined time period monthly. To ensure the implementation of GMP, GDP practices and review of issues and impact of the same, if any, and take corrective actions. To ensure the investigation for complaints and deviations and CAPA after reviewing instruments. To prepare, review, Implement and update SOPs according to current regulations systems. To review Master Batch Document (MBD) / Master Packing Document (MPD) and get approval in advance from Head of Department of Production & QA. To train/...

Lead UNIT QA focusing on QA PROCESSES, REJECTION ANALYSIS, QUALITY COSTING, CALIBRATIONS, PROCESS AUDIT, PRODUCT AUDIT, LAYOUT INSPECTION, FINAL INSPECTION, CUSTOMER QA, CUSTOMER COMPLAINTS HANDLING, QUALITY COMPLIANCES etc INJECTION MOLDING QA must Required Candidate profile DME/BE/CIPET 10+yrs exp with any PLASTIC / IM Unit into QA having strong exposure in IPQA, CQC, SQA, QMS etc Apply only if u hv exp in INJECTION MOLDING for CONSUMER DURABLES/AUTOMOTIVE applications Perks and benefits Excellent Perks. Send CV to jobs@adonisstaff.in

You will be responsible for conducting In-Process Quality Assurance (IPQA) activities on the shop floor throughout the various stages of sterile manufacturing and packing process. This includes performing sampling at each stage or when necessary during product manufacturing, filling, and packaging activities. Your duties will also involve conducting in-process checks of manufacturing, filling, and packaging processes. You will be required to perform Acceptable Quality Level (AQL) checks after completing visual inspection of products. Additionally, you will need to carry out audit trail and electronic data reviews batch-wise and as per the designated schedule. Furthermore, you will be tasked ...

Purpose of Job 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 Skill Required Participate in the creation and execution of the risk-based audit plan, reporting results to Intas Leadership and the Audit Committee of the Board of Directors. Conduct a wide-ranging scope of audits with an emphasis on assessing emerging areas of risk including revenue recognition, contract accounting, compliance, fraud, operations and o...

Skill Required Chartered Accountant with 3 - 5 years of post-qualification experience (Assistant Manager), 1-3 years of post-qualification experience (Senior Executive) in external or internal auditing. Experience in Big 4 or a global organization will be preferred. Highly motivated and self-driven with limited guidance from the supervisor. Experience in data analytics in audit lifecycle. Strong working knowledge of financial, operational, compliance, and systems auditing techniques. Strong verbal and written communication, report drafting, and presentation skills, and proficiency with the English language. Ability to think outside the box and challenge the status quo. Must be able to work i...

Skill Required Roles and Responsibilites 1. Media fill and qualification summary preparation knowledge. 2. To maintain track of qualification and validation activities. 3. To prepare and review the protocols and reports. Execution of various qualification / validation activities. 4. To review correctness of the technical documents received from the supplier (DQ/OQ/IQ/PQ,FAT). 5. Co-ordinate with production and other user department for qualification/validation activities 6. Timely compile and review of qualification validation reports. 7. To review the equipment documents like calibration reports and ensure correctness of documents. 8. To perform FAT. 9. To co-ordinate with outside agencies ...

Purpose of Job 1. Preparation and Review of PQR. 2. Statistical evaluation of identiifed CPP & CQA at Manufactuirng and Quality Control stage using Minitab software. Skill Required 1. Having basic knowledge on Microsoft Word and Microsoft Excell 2. Have knowledge of Minitab software for statstical evaluation of data. Roles and Responsibilites 1. Preparation and review of PQR schedule. 2. Planining of PQR compilation as per PQR schedule. 3. Collection of data from all the CFT teams for compilation of PQR. 4. Statistical evaluation of identiifed CPP & CQA at Manufactuirng and Quality Control stage using Minitab software. 5. Based of the PQR data recommendation to be recommended to concern depa...

Purpose of Job 1. Preparation of PQR. 2. Statistical evaluation of identiifed CPP & CQA at Manufactuirng and Quality Control stage using Minitab software. Skill Required 1. Utilization of Microsoft Word and Microsoft Excell 2. Using of Minitab software for statstical evaluation. Roles and Responsibilites 1. Preparation of PQR schedule. 2. Planining of PQR compilation as per PQR schedule. 3. Collection of data from all the CFT teams for compilation of PQR. 4. Statistical evaluation of identiifed CPP & CQA at Manufactuirng and Quality Control stage using Minitab software. 5. Based of the PQR data recommendation to be recommended to concern department and ensure implemenation of the same. Quali...

Roles and Responsibilites 1.In process Quality Assurance activity in Production and warehouse area 2.Provide line clearance as per SOP 3.Monitoring and QA rounds in production and Warehouse 4.Sample verification against TRF / BPCR 5.Carry out Semi-finished / finished product sampling for release, stability study and control samples 6.To send samples along with TRF to Quality control laboratory 7.Participate in media fill, process validation, cleaning validation activities as per requirement 8.Timely communication and co-ordination with all the stake holders 9.Participation in Change control, Deviation & Investigations as per requirement 10.Preparation / review of documents like; SOPs, risk a...

Job Description Required for IPQA acitities. Required for Batch manufacturing record review. Required for line clearnace and other shop floor related activity of QA. Work Experience 3 to 8 years. Education Graduation in Pharmacy Competencies

SKS Enterpprises is looking for Portfolio Review Analyst to join our dynamic team and embark on a rewarding career journey Analyst plays a crucial role in driving data-driven decision-making processes within the organization This position involves analyzing complex data sets, generating actionable insights, and providing strategic recommendations to support key business initiatives Key Responsibilities:Data Analysis:Conduct in-depth analysis of large and complex datasets to extract meaningful insights Utilize statistical and data visualization tools to present findings in a clear and concise manner Strategic Planning:Collaborate with cross-functional teams to understand business objectives a...

Perform in-process quality checks during manufacturing and packaging stages Ensure compliance with GMP, ISO, and regulatory standards Review and verify batch manufacturing and packing records Identify and report non-conformances, and implement corrective and preventive actions (CAPA) Conduct line clearance, sampling, and documentation as per SOPs Coordinate with production, QC, and warehouse departments to ensure product quality Maintain documentation for internal audits and regulatory inspections Provide on-the-floor training to production staff on quality protocols Help maintain quality-related documents and SOPs. Support in internal audits and regulatory inspections.

In Process Monitoring, GMP Compliance, Verfication of Online Documentation

Job Responsibilities : Planning: Plan for Immediate response to all emergency calls including mock drills Fire safety inspection round of the plant as per schedule, Assurance: Apply Incident Command & Control technique for emergency control & mitigation, Response to emergency and actively participate in Fire Fighting/rescue operation, Carryout ITM of all firefighting equipment/systems & performance stand by duty during critical jobs, Check and maintain the fire vehicles and jeeps, Compliance: Ensure compliance with fire safety standards, procedures and checklist Maintain Log book, Occurrence book and other shift related documentation, Good discipline and conduct in fire station Education Req...

Intermediate batches release in SAP. All SAP related changes are tested on development server, quality server and then implmeneted on Production server e.g. MQC testing and implementation, preparation of test scripts for all SAP changes, updation of master documents numnbers in SAP, updation of overages symbols in SAP, MSCN2 changes in SAP. Food control sample review. Issuance of packing material COfA for all interlocations transfers. For Raw materials also this activity will start now. Checking of goods during dispatch of product at BSR level after repeated complaints from Vietnam of theft. Shipper weight checking before transfer to FG BSR. Measuring cylinder calibration. 8. Micro sample fo...

Seeking a IPQA Executive to ensure skincare products meet regulatory, safety & 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

Dear Applicants, Greeting from Biophore India pharmaceutical Pvt Ltd, We have opening for Formulation DQA Department Development Quality Assurance / Formulation Quality Assurance R&D: Handling of QMS documents and Ensure the SOP compliance Review of Formulation Analytical Development Documents & Formulation Product Development Documents. Method Validation and Transfer Protocols and Reports Product development with QbD approach Responsible for ensuring GMP/GLP/GDP compliance in the Formulation and Analytical areas as per the respective SOPs. Review of FRD activities (LNBs, BDRs, PDRs, MFRs and MPR) SOPs and Guidelines Preparation and Review and Approval of SOPs. Responsible for conducting Int...

Hi we are hiring Position ;- Sr. Executive IPQA Experience- 5-10 years Salary Package- 5-8 LPA Should have worked in Injectable Unit Need to handled the whole IPQA Team

MetLife is looking for Software Dev Engineer Test II to join our dynamic team and embark on a rewarding career journey Analyzing customer needs to determine appropriate solutions for complex technical issues Creating technical diagrams, flowcharts, formulas, and other written documentation to support projects Providing guidance to junior engineers on projects within their areas of expertise Conducting research on new technologies and products in order to recommend improvements to current processes Developing designs for new products or systems based on customer specifications Researching existing technologies to determine how they could be applied in new ways to solve problems Reviewing exis...

EXL Services.com ( I ) 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 personnel a...