1357 Ipqa Jobs - Page 12

• To maintain and adherence of the GLP and safety procedures in laboratory. • To perform the analysis as per work allocation and records the results in work sheet (Protocols) for raw material / packing materials/intermediates /APIs/ Stability and etc.. as per current specification and method of analysis. • To work as Analyst and maintain the CFR 21 part -11 compliance by following laid down procedures. • To perform all the HPLC related analysis and perform the online documentation for In-process, intermediate, finished products & returned goods / raw materials Hold time / Stability study / working standard analysis as per laid down specification & test procedures , SOPs, as per work allocati...

• To plan and provide the analysis support as per approved specification & test procedure and standard operating procedures. • Ensure that, all the analysis as per customer specification is done (for dispatch) as per the planning (planning to be taken as per delivery instruction). To review and monitor daily activity of dispatches and report to Quality Control Head • To approve/reject raw material/packing material based on the analysis data. • To approve / reject the intermediate and finished product based on the analysis data. • Review and approval of certificate of analysis for raw material, packing materials, intermediates and APIs. • To plan for Joint analysis with R& D personnel during ...

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 Maintece 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. 6.To review Batch Manufacturing Records / Batch Packing records. 7.To participate Training programs of various cross linked SOPs and effectively ensure its implementation.

WALK-IN INTERVIEW | ZYDUS LIFESCIENCES LIMITED API Plant Dabhasa | Production & Quality Assurance Dear Candidate, Greetings from Zydus HR team!! Zydus Lifesciences Limited, The Zydus Group with an overarching purpose of empowering people with freedom to live healthier and more fulfilled lives, is an innovative, global life-sciences company that discovers, develops, manufactures, and markets a broad range of healthcare therapies. The group employs over 26,000 people worldwide and is driven by its mission to unlock new possibilities in life-sciences through quality healthcare solutions that impact lives. The group aspires to become a global life-sciences company transforming lives through path...

Dear Applicants, Greeting from Biophore India pharmaceutical Pvt Ltd, We have opening for Formulation - DQA Department(OSD/Injectable) Job Description: 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, BDR’s, PDR’s, MFR’s and MPR’) SOP’s and Guidelines Preparation and Review and Approval of SOP’s. Responsible for conducting Internal Audits/External Audi...

Role & responsibilities 1. Follow the instruction & procedure given in Entry-Exit SOP (Standard Operating Procedure) of production area. 2. Follow the personnel hygiene practices in factory premises. 3. Responsible for monitoring of temperature, relative humidity and differential pressure of laminar air flow units and pass boxes. 4. Responsible for handling of material movement in production area. 5. Responsible to maintain the document as per Good Documentation Practices and area as per Good Manufacturing Practice. 6. Responsible for training to trainee chemist, operator, cleaning persons and workers on their respective job. 7. Responsible to maintain the day to day activity. 8. Responsible...

Role & responsibilities : 1. Perform IPQA activities at the shop floor during the manufacturing and packing processes. 2. Conduct QA overview for cleanroom behaviour and personnel hygiene compliance. 3. Review batch processing records for accuracy and compliance with standard operating procedures. 4. Review all manufacturing, packaging, and analysis-related documents to ensure completeness and adherence to regulatory requirements. 5. Familiarity with Annual Product Quality Review (APQR) and Continued Process Verification (CPV) processes. 6. Review documents and logbooks of respective areas to ensure adequacy and completeness. 7. Collaborate with cross-functional teams to address any quality-...

QMS, Deviation, CAPA, knowledge of regulatory audits, Validation, APQR, IPQA. Process validation. Review of protocols for qualification and validation of facility/ equipment / product / process. Review of validation reports. Required Candidate profile 4 years plus experience preferably in injection manufacturing plant.

Interview on 11-11 in Bharuch for QA - Male/Feamle Bsc/Msc Chemistry 3 to 10yr exp 5.5 LPA Apply : sdpbharuch@gamil.com sub : QA Dahej Inetrview Date : 11-11-2025 Time : 9 to 4 Job Location : Dahej . Required Candidate profile OUR BHARUCH OFFICE FOR CALL LETTER SDP HR SOLUTION 610,GOLDEN SQUARE OPP HOTEL REGENTA ABC CIRCLE BHARUCH We Provide Best Jobs in Gujarat Free Requirement !!

Roles and Responsibilities Develop and implement quality management systems (QMS) to ensure compliance with regulatory requirements. Conduct process validation, IPQA, and validation testing to ensure product quality. Collaborate with cross-functional teams to identify areas for improvement and implement changes. Ensure effective communication of quality policies, procedures, and expectations throughout the organization. Provide training on QMS principles and best practices to employees. Desired Candidate Profile 10-19 years of experience in pharmaceutical industry with expertise in Quality Assurance/Quality Management Strong understanding of GMP regulations Experience in developing and imple...

Requirement of following candidates: 1) B. Pharm/ M. Pharm - for production, QA (male candidates preferred) 2) B.Sc/ M.sc - for QC (male/ female both preferred ) 3) B. tech/ M. Tech - for engineering (only male candidates)

Production - Senior Officer -Fermentation upstream opertor. Should have experience in Aseptic practices, Handling of Fermenter, Process vessels, Homogenizer, TFF systems, Filtration, Biosafety cabinet. Microbial fermentation experience. Manufacturing activities according to effective SOPs. Batch related documents in manufacturing area. Readiness related to batch manufacturing. Execution of activities in compliance to cGMP. Execution of activities during campaign change. Decontamination and disposable of bio waste. Preparation of URS for the equipment. Preparation of MCB/WCB. Automated or manual CIP of all the equipment in the manufacturing area. Follow safety norms in the manufacturing depar...

Location - Parwanoo, Himachal Pradesh Job Description: We are seeking an experienced Assistant Manager SQA to manage and improve supplier quality performance. The role involves conducting supplier audits, evaluating processes, and ensuring compliance with ISO/IATF standards. The ideal candidate should have strong knowledge of forging processes, core quality tools, and supplier development methodologies to ensure consistent quality and on-time delivery from vendors. Key Responsibilities: Conduct supplier process, system, and product audits (PPAP) and ensure timely closure of non-conformities. Implement and monitor supplier quality improvement plans. Evaluate supplier performance and provide f...

Role & responsibilities Quality Documentation & Compliance: Handling and preparation of GMP-related documents including Change Controls, Deviations, OOS, CAPA, Lab Incidents, APQR, and Investigations, with diligent follow-up to ensure timely closure. Document Management: Management and handling of Cell Bank documentation and Technology Transfer documents to support regulatory and operational compliance. Validation & Review Activities: Review of Process Validation and Cleaning Validation protocols and reports, Batch Manufacturing Records (BMR), and Continued Process Verification (CPV) data to ensure accuracy and alignment with regulatory expectations. CPV & PQR Analysis: Handling of JMP softw...

Hikal Ltd is looking for Officer to join our dynamic team and embark on a rewarding career journey Ensure smooth execution of operational and administrative tasks Support management in compliance, reporting, and daily operations Monitor work processes and suggest efficiency improvements Maintain accurate documentation and uphold company policies Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before

QA Documentation Validation / Qualification Documents Control and Archival of documents Retain Sample Handling and Observation SOP Preparation and Revision related Activities BMR Preparation and Review Monitoring of all the QA activities, test results, leaked defects, and identifying areas of improvement. Handling of QMS Related Activities (change control, deviation, Market Complaint, incident, OOS). Knowledge of regulatory guidelines and requirements, such as FDA, MHRA, and ICH & ISO Standard.

To check documents like equipment log books, temperature & humidity records, Collect in-process and Finished sample as per Specifications and Protocol. Supervision of RM/PM Sampling and dispensing procedure. Machine Line clearance of Production Area. Area Line Clearance of Production area Checking online tablet weight variation, hardness, friability, thickness & DT Time & check informality of weight. Verification of granulation, Compression, Coating, & Packing process & also release for same. Able to fill And Check BMR. Able to Give Batch Approval, verify various Documents. Able to finalize Quality of Finished goods. DOCUMENTATION

To ensure implementation of QMS in the plant, handling QA(IPQA), prepare & review all documents, SOP’s, BMR, BPR, qualification & validation protocol, carryout details Investigation, Change control, Deviation, OOS.

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...

Manage day-to-day office operations, including administrative tasks and employee coordination. Handle communications, both internal and external, ensuring timely responses and follow-ups. Organize meetings, prepare agendas, and take minutes for effective documentation. Maintain office supplies and ensure all equipment is in working order. Assist with budgeting, invoicing, and other financial tasks as needed.

shall be responsible for maintaining and improving all QMS activity, GMP and GLP across the company Handling QMS activities like change control, validations, stability, qualifications, APQR and Risk assessment etc Label artwork review and management Required Candidate profile Assisting HOD in customer complaint analysis and preparation of customer complaint report. Investigation of incidents, deviations, OOS and ensure corrective actions in place.

We are seeking an experienced and skilled IPQA personnel to join our pellet manufacturing facility. The ideal candidate will possess a thorough understanding of process LC activities analytical review doc. related to pharmaceutical OSD formulations

Roles and Responsibilities Ensure compliance with BMR, SOPs, and quality standards through regular audits and inspections. Develop and maintain documentation for QA procedures, protocols, and reports. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Maintain accurate records of batch manufacturing processes, including BPR reviews.

Hikal Ltd is looking for Officer to join our dynamic team and embark on a rewarding career journey Ensure smooth execution of operational and administrative tasks Support management in compliance, reporting, and daily operations Monitor work processes and suggest efficiency improvements Maintain accurate documentation and uphold company policies Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before

Kotak Mahindra Bank Limited is looking for 811-CEC Officer-Outbound-Digital Banking Kotak 811-Contact Centre Outbound to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to achieve strategic outcomes Apply subject expertise to support operations, planning, and decision-making Utilize tools, analytics, or platforms relevant to the job domain Ensure compliance with policies while improving efficiency and outcomes Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their o...