1062 Ipqa Jobs - Page 16

As a QA (Quality Assurance) /Test Developer you will be designing better ways to identify potential weak spots, inefficiencies, and issues within software systems. This position will work closely with development teams and other test engineers in the implementation and delivery of software products that meet rigorous quality standards, budgets, and timelines. The role seeks good levels of personal organization, and the ability to work well with a distributed global team in a fast paced and exciting environment. You will play a key role by delivering quality functions for development teams within test driven framework. Your scope will include Test Plan Development, Test Case Execution, Automa...

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office Job Description At Thermo Fisher Scientific Inc., we are seeking an ambitious and dedicated QA professional for the position of band 3 (direct labour). This role is pivotal in our mission to maintain world-class quality standards and ensure flawless operations. Join us and be part of a team that is determined to make a difference! Responsibilities Manage material receiving, destruction, in-process quality assurance (IPQA), and return activities Perform and conduct quality checks (IPQA) at decided intervals during packaging production Maintain the Archival Are...

Walk In Drive Quality Assurance Department In Formulation Division @ Kothur Department :- Quality Assurance OSD Qualification :- B Sc | B Pharmacy | M Pharmacy | MSC Experience :- 2 to 8 Years Skills:- AQA | IPQA|CQA| IPQA MFG|IPQA Packing Division :- Formulation Interview Date:- 13-09-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location:- MSN Laboratories Pvt Ltd,. Formulation Unit-02,Kothur, Nandigama. Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume ,Increment Letter,Payslips, Bank Statement, Certificates,Aadhar Card & Pan Card We are looking for candidates those who have experience in QA OSD (IPQA,AQA,Packing,Documentation,Valid...

Core expertise in IPQA, 21 CFR compliance, validation & qualification, E-BMR/E-Log, QMS, risk assessment; skilled in audits, regulatory compliance, team management, training, and digital quality systems. Required Candidate profile B/MPharma 7 - 10 years of experience

Job Description 1. Preparation and review of operational packing materials list, Packaging materials specifications, Packaging materials specifications base documents, BOM, BPR (PAS X and SAP), In House Labels for Exhibit Batches, Pack Split Up and Pallet Matrix. 2. To provided technical support to Production, QA, QC and RA. 3. Review of Artwork, Shade cards and print proof etc. Initiate Change controls, Deviation and CAPA and close all action item of change control, CAPA and deviation within time frame preparation of investigation report of deviation. Coordinate with R&D and QA for Primary Packaging Materials Specifications, Primary Pack Specification and Standard Test Procedures. 4. Prepar...

Exp. in IPQA, line clearance & digital documentation w/ E-BMR & E-Log. Equipment qualification & process validation, w/ an understanding of 21 CFR Pt. 11 & audits. Risk assessment, CAPA management & conducting internal & vendor audits. Tech Transfer Required Candidate profile 10-15 Yrs B. Pharma / M. Pharma

Exp. in IPQA, line clearance & digital documentation w/ E-BMR & E-Log. Equipment qualification & process validation, w/ an understanding of 21 CFR Pt. 11 & audits. Risk assessment, CAPA management & conducting internal & vendor audits. Tech Transfer Required Candidate profile 10-15 Yrs B. Pharma / M. Pharma

Job Description Join Lupin Limited's dynamic Quality division as an Officer within our Validation department based in Pithampur. In this pivotal role, you will take charge of the cleaning validation activities for our API and Formulation facilities. Your responsibilities will encompass comprehensive management and execution of validation protocols supporting our commitment to the highest quality manufacturing standards. Your core duties will include ensuring rigorous residue cleaning validation processes to maintain contamination-free production environments. You will manage and evaluate nitrosamine and genotoxic cleaning validation activities, essential to safeguarding product safety and re...

General Summary: Job Overview This is a unique opportunity to join Qualcomms finance and accounting organization based in Hyderabad in the Corporate Internal Audit & Advisory Services (IA & AS) team. The department focuses on assisting the Audit Committee and management teams in the improvement of processes that manage risks related to achieving Qualcomms business objectives. Using Qualcomms risk-based audit methodology, the senior auditor will assist in the execution of internal audits. Specifically, the responsibilities include: Providing U.S. based time zone coverage as needed (up to 50% of time) Supporting the creation of initial planning memos and process flowcharts Identifying and asse...

Responsible for IPQA, line clearance, preventive maintenance checks, BMR/BPR review, vendor qualification, audit support, QAMS documentation, APQR preparation, and compliance verification across departments. Required Candidate profile M.Sc or M.Pharm or BSc or BPharm 2-3 Years 2.5 to 3.5 LPA

1. Monitor raw material dispensing activity. 2. Perform daily IPQA activities as per SOP-defined frequency and ensure timely closure of IPQA observations. 3. Conduct validation sampling as per approved validation protocols. 4. Review BMR (Batch Manufacturing Record) and BPR (Batch Packing Record) for accuracy and compliance. 5. Perform ERP-related transactions of IPQA. 6. Check BSR (Batch Summary Record) and Shipper inspection as per SOP. 7. Manage issuance, review, and reconciliation of formats across all departments. 8. Conduct IPQA rounds and share observations with concerned HODs for corrective action and compliance. 9. Ensure cleaning, sanitation, and hygiene in all departments to maint...

Line Clearance for Dispensing, Manufacturing & Packing activities Dispensing of RM/PM for batch Mfg Monitoring of IPQA activities (Granulation, Blending, Capsulation, Compression, Coating, Packing Sampling of IP and FP Samples Batch documents review

Nexdigm (SKP) is looking for Senior Executive - FDD 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 implementi...

To execute of Production activities machine wise in Granulation Area. Online Checking of in process parameters & completion of the Log book and BMR of Granulation Area To check and make availability of machine as per PM Schedule. Co-ordination with IPQA/QC/Engineering department for smooth functioning of Production activities. Handling of SAP related work in Production To fill documentation as per cGMP practice in Production area. To do calibration of balances in Production area. Proper shift handover to the next shift officers to fulfill the production monthly target. Manpower utilization in the Production Department Imparting various training to officers and workers To fill the daily asses...

To execute of Production activities machine wise in Granulation Area. Online Checking of in process parameters & completion of the Log book and BMR of Granulation Area To check and make availability of machine as per PM Schedule. Co-ordination with IPQA/QC/Engineering department for smooth functioning of Production activities. Handling of SAP related work in Production To fill documentation as per cGMP practice in Production area. To do calibration of balances in Production area. Proper shift handover to the next shift officers to fulfill the production monthly target. Manpower utilization in the Production Department Imparting various training to officers and workers To fill the daily asses...

Esskay Compu Services 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 and ...

IPQA, IPQA Officer, IPQA Chemist ,GPM,BMR SOP, Pharma Process, FDA Approval, COsmetic Healthcare Industry, Direct Call:9974756637 whatsapp Resume:9974756637

Job Description Department: Production Designation: Jr. Officer - Production (E0) Working Section: Granulation / Compression / Coating Comply with all cGMP, GxP and any other applicable regulatory requirement, including EH&S requirements. Complete training on relevant SOPs and develop an understanding of the activities to be conducted prior to undertaking any task. Conduct all tasks/activities as per the applicable SOPs. Report any difficulty or deviation in following the procedure/instruction to immediate supervisor/managers. Report any quality concern or suggestion for improvement to supervisors/ managers. Manufacturing / processing of batches of assigned products under supervision as per ...

Line Clearance for Dispensing, Manufacturing & Packing activities Dispensing of RM/PM for batch Mfg Monitoring of IPQA activities (Granulation, Blending, Capsulation, Compression, Coating, Packing Sampling of IP and FP Samples Batch documents review

Working Hours - 8 Hrs Role & responsibilities Dispensing, Manufacturing, Packaging and Dispatch activities. -Review and control of SOPs, BPR Issuance,Cleaning Validation,Line Clearance. -Master Formulae and records. -Good Documentation as per GLP,Preparation. -Review of process validation protocols and reports. -Familiar with Production machinery, Production floor working, pH meter, Refractometer, and GLP.

Job Description Key Responsibilities 1. Monitoring of IPQA activities in all functional departments. 2. Responsible for BMR correction/ quantity verification before batch execution along with QC. 3. Responsible for area and line clearance in production area. 4. Responsible for BMR verification for the completion and online inspection of batch execution at site. 5. Responsible for dispatch verification along with dispatch checklist, BMR, labels (at site and godown) 6. Site inspection for any abnormalities with respect to Raw materials, Packing materials, Products, labels, BMR, Dispatch. 7. Responsible for implementation of 5S at site. 8. Handling of Deviations, failure investigation, Change m...

Global Study Centre (GSC) is looking for Documentation Assistant to join our dynamic team and embark on a rewarding career journey Prepare, organize, and manage company documentation and records. Ensure documents are properly filed, easily accessible, and securely stored. Assist in the creation and revision of company policies, procedures, and manuals. Coordinate with various departments to gather and verify documentation. Maintain documentation databases and ensure data integrity. Prepare reports and summaries as needed for management review. Candidates of with proficiency in English and work experience are preferred. Freshers can be applied for the post of trainees.

Walk-in Drive @ Sanand, Ahmedabad location for Quality department (EM, Micro Testing & IPQA) for Injectable plant on 7thSep25 (Sunday). We are looking for suitable candidates for injectable/ sterile manufacturing plant for Ahmedabad location. Interview Venue Details: Date: 7thSep25 (Sunday) Time: - 9:00 AM to 2:00 PM Venue : Amneal Pharmaceuticals Pvt. Ltd. Plot No: 161/1, Sanand Bavla Highway Road, Village : Pipan, Sanand, Ahmedabad, Gujarat 382110 JOB LOCATION: Sanand, Ahmedabad 1. Quality Assurance - Environmental Monitoring (Microbiologist) Designation : Trainee/ Officer/ Sr. Officer / Executive Department : EM (Environmental Monitoring) Qualification : B.Sc. (Micro) / M. Sc (Micro) / B....

Job Title: Assistant Manager In-Process Quality Assurance (IPQA) Department: Quality Assurance Location: Hyderabad, Jeedimetla Reporting To: Manager Quality Assurance / Head Quality Job Purpose: To ensure that all in-process operations are monitored and compliant with applicable cGMP, SOPs, and regulatory requirements. The IPQA Assistant Manager is responsible for in-line quality checks, deviation control, batch record review, and timely escalation of non-conformities during manufacturing and packaging processes. 1. In-Process Quality Monitoring Supervise and execute IPQA activities during manufacturing and packaging. Perform real-time line clearance, process checks, and verification. Ensure...

Sr. Executive- Talent Acquisition is responsible for driving the recruitment team to meet and exceed hiring targets within defined timelines while ensuring process adherence, data accuracy, and high-quality delivery. The role demands strong leadership to manage team productivity, skill development, and performance enhancement. This individual will work closely with TA vertical leads to execute strategic hiring plans, foster diversity hiring, and streamline recruitment processes for better efficiency and stakeholder experience. Key responsibilities include monitoring and reporting performance metrics (SLA, source mix, compliance, quality), promoting effective communication within the team, en...