243 Ipqa Jobs - Page 6

Job Summary Roles & Responsibilities Review and approval of all analytical test data of Quality control. Review and usage decision of analytical reports in LIMS, Empower and SAP. Electronic signatures level-2 for chromatography data station (CDS) and standalone instruments. Review the Analytical test report in LIMS. Review the reported results against specification and trends. Review the method validation and method transfer documents. Review the instrument calibrations and working standard qualification records. Handling the Incidents/ Deviations, Out of Trends, Out of Specification including investigations, Corrective and Preventive actions follow up and closure. Monitoring of analytical activities in Quality control laboratory. Verification of Specifications/standard test Procedures/Worksheets/Analytical Reports before Approval. Verification and review of the audit trails for Standalone, Empower and LIMS. Ensure cGMP / cGLP compliance. To follow Safety, Health and Environmental procedures and practices. Review and approval of excel sheet validations. Review results acceptance for API and Excipients and Packing material. Review of compiled of Stability Data and its verification/ Exhibit batch sampling protocols. Handling of Robotic Process Automation of Chromatography Data review (RPACD) To carry any other activities assigned by upward reporting staff. Qualification Educational qualification: A Bachelor’s/Master's degree in Pharmacy, Chemistry, Chemical Engineering, or a related field Minimum work experience : 3 to 7 years of experience in QC or AQA department is mandatory. Additional Information About the Department Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Inspection and verification of In-process activity in Manufacturing Area. Monitoring of Handover Activity of ARM/Bulk. Verification of Packing and Dispatch activity for Final ARM/Bulk. Issuance of Cell Bank / Issuance of Reference standard.

Position Deputy Manager - Quality Assurance Experience: 7 - 14 Yrs Function: Product & Technology Development Primary Responsibilities: The incumbent will be responsible for the design, implementation, and verification of quality systems across food manufacturing units. Key duties include centralized monitoring of key process and quality performance indicators and reporting through the Management Information System (MIS). The role also involves preparing detailed product trial quality reports and compiling comprehensive documentation (dockets) to facilitate technology transfer to production units. Requirements: Proven knowledge and experience in food quality system design, implementation, and verification. Strong understanding of process control validations in relation to product performance. Familiarity with food safety standards and protocols, including HACCP, ISO, GMP, and related frameworks. Exposure to process automation and quality automation systems is highly desirable. Proficiency in preparing and managing documentation related to quality systems and food safety plans, including procedures and standardized formats. Prior experience in a production environment will be considered an advantage. Competency in using software applications for effective MIS reporting is essential.

Job Description 1 Should have knowledge of dispending of RAW materials. 2. Should have exposure to SAP system. 3. Should have exposure to regulatory plant. 4. Should be able to read & write English. Work Experience 3- 6 year Education Graduation in Arts Competencies

Responsibilities: * Ensure compliance with regulatory requirements through quality control measures * Conduct process validations, cleaning verifications & change controls * Prepare validation protocols & reports

Job Description Candidate should the exposure for handling the Bottle packing line. Should have the work experience in Regulatory plant. Faced the USFDA, MHRA,TGA inspection. Good Communication skill. Having the SAP knowledge. Work Experience 3 to 05 years' Experience. Education Graduation in Pharmacy Competencies

03 - 06 years experience of external preparations, Ointment and OSD IPQA activities Job Responsibilities - - Totrack batches for process validation, packing validation and hold time study. Certificationof Appropriate and timely Line-Clearance for Manufacturing, Packing, Dispensing Tocarry out the online checks& to take on line SAP entries. - ToWithdraw & Submit the Samples (Analysis SFG and FG & Control samples,Validation, Regulatory, R&D, Hold time study & Micro samples) toConcern Dept. as & when required. - Toensure the cGMP on the shop floor and to highlightthe on line Problems / Non Conformances with the respect to Procedures,Specifications, SOPs, cGMP etc. on day to day basis Numbers ofcritical/major nonconformance noticed. OnlineBPR, Logbooks completion & Review of documents like Preventive calibrationrecords, daily/weekly quarantineregister etc. in the Concerned dept. - Issuanceof Batch Manufacturing Records and Batch Packing Records to productiondepartment. - Reviewof Executed Batch Manufacturing Records and Batch Packing Records Toverify online finished goods before transfer to BSR.

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

Dear Candidates, Greetings from KEYBIZ DASHBOARDS, We are looking for Quality Assurance Executive & Sr.Executive injectables&OSD for one of our reputed pharmaceutical client, based at Hyderabad & Vizag location. Please find below openings list. 1.IPQA 2.QMS 3.AQA 4.Validation 5.Equipment Qualification 6.CSV 7.Market Complaints. The above positions we are looking for Hyderabad & Vizag locations, interested please share us updated cv to prasanthi@mydashboards.in or feel free to call on 6305391924 Thanks and Regards Prasanthi - Dashboards Team HR

Roles and Responsibilities QA 1. Well knowledge about cGMP. 2. Strong knowledge in IPQA Production as well as packing. QC 1. CANDIDATE SHOULD HAVE KNOWLEDGE OF GLP 2. REQUIRE KNOWLEDGE IN HPLC. 4. MAINTENANCE OF STABILITY CHAMBERS, STABILITY SAMPLES, STABILITY SCHEDULES, STABILITY REPORTS. 4. ANALYSIS OF RAW MATERIALS,PACKING MATERIAL, CLEANING VALIDATION, CLEANING VERIFICATION, INTERMEDIATES, BULK, FINISHED, STABILITY SAMPLES AND OTHERS AS REQUIRED. 5. PERFORM THE DAILY CALIBRATION OF THE BALANCE, PH METERS AND OTHER INSTRUMENTS AND ENSURE THE RECORDS ARE UPDATED. 6. PREPARATION OF SPECIFICATION, STANDARD TESTING PROCEDURES, ANALYTICAL PROTOCOLS AND REPORTS. Desired Candidate Profile 3-10 Year Experience with B.Pharm and Podicherry.

API -QA

Job Summary Roles & Responsibilities Review and approval of all analytical test data of Quality control. Review and usage decision of analytical reports in LIMS, Empower and SAP. Electronic signatures level-2 for chromatography data station (CDS) and standalone instruments. Review the Analytical test report in LIMS. Review the reported results against specification and trends. Review the method validation and method transfer documents. Review the instrument calibrations and working standard qualification records. Handling the Incidents/ Deviations, Out of Trends, Out of Specification including investigations, Corrective and Preventive actions follow up and closure. Monitoring of analytical activities in Quality control laboratory. Verification of Specifications/standard test Procedures/Worksheets/Analytical Reports before Approval. Verification and review of the audit trails for Standalone, Empower and LIMS. Ensure cGMP / cGLP compliance. To follow Safety, Health and Environmental procedures and practices. Review and approval of excel sheet validations. Review results acceptance for API and Excipients and Packing material. Review of compiled of Stability Data and its verification/ Exhibit batch sampling protocols. Handling of Robotic Process Automation of Chromatography Data review (RPACD) To carry any other activities assigned by upward reporting staff. Qualification Educational qualification: A Bachelor’s/Master's degree in Pharmacy, Chemistry, Chemical Engineering, or a related field Minimum work experience : 3 to 7 years of experience in QC or AQA department is mandatory. Additional Information About the Department Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Company Details Job Title Job Description Competencies Over all personality Awareness about the changing business environment and the demand on performance. Communication Interactive Skills Team spirit and Cohesiveness Learning, Self-Development and Achievement Orientation Visible energy level, capability to stretch and adaptability to company culture. Academic/Professional Qualifications Work experience in the functional area Job Knowledge specific to the position Planning, Organizing and Problem Solving

To prepare and issue SOPs. BMR / BPR verification. Verification of Rejected Material in Stores. To check calibration status of production instruments/ equipments periodically. To perform the in process analysis. Required Candidate profile To give line clearance during product change over. To supervise the dispensing of raw materials. To organize and collect the ln process, intermediate and Finished Product samples during Manufacturing.

Open Positions: Officer / Executive / Sr Executive Quality Assurance & Quality Control : Analytical Skill on HPLC, Electrophoresis, Microbiology, Document Review, IPQA, Quality Systems, GMP Compliance, QA-QMS Biosimilars Manufacturing: Downstream (Operation of Chromatography systems) & Upstream (Handling of Single use and Stainless-steel bioreactors) Experience: 2 to 10 years of relevant experience in Biopharmaceutical Qualification: B Sc / B. Pharm/B Tech / M Sc in Microbiology / Biotechnology / Chemistry/M. Pharm Date : 01st June 2025, Sunday Time : 08:30 AM to 06:00 PM (Registration will be closed by 12:00 PM) Venue : Hotel Pride , 5, University Rd, Narveer Tanaji Wadi, Shivajinagar, Pune, Maharashtra 411005, India Note: All positions are based out at Pune, Gotawade.

Roles and Responsibilities Conduct quality control tests on raw materials, intermediates, and finished products using techniques such as HPLC, GC, FP, IP, Stability studies. Ensure compliance with cGMP guidelines and maintain accurate records of testing results. Investigate market complaints and perform microbiological analysis to identify root causes. Develop and implement quality assurance procedures for OSD formulations. Collaborate with cross-functional teams to resolve issues related to dissolution testing.

WALK-IN INTERVIEW ALERT JD Join the growth journey with Opes Healthcare Location: 3rd Floor,Tulsi Plaza, Changodar, Ahmedabad. Date: 25th May 2025 (Sunday) Time: 09:00 AM to 02:00 PM Multiple Job Openings at Opes Healthcare-Ahmedabad. Were hiring passionate and dynamic individuals across multiple departments! Open Positions: 1. IPQA :Monitor all process check/Line Clearance/cGMP/Documentation Officer to Sr. Executive. B.Pharm/ M.Pharm | 02–07 yrs 2. Quality Control: RM Testing/HPLC/GLP/Documentation – Officer to Sr. Executive. B.sc/M.sc/B.Pharm/ M.Pharm | 02–07 yrs 3. F&D: Design & Develop formulation/Process Optimization/cGMP/Documentation/ – Officer to Sr. Executive. B.Pharm/ M.Pharm | 02–07 yrs 4. ADL: Stability Studies/HPLC/GLP/Documentation/Method Development – Officer to Sr. Executive. B.Sc/M.Sc/B.Pharm/M.pharm | 02–07 yrs 5. Production(Third party operation): Audit to Other company/Production planning/Material control/QMS-Officer to Sr. Executive. B.Pharm/M.pharm | 02–07 yrs 6. Purchase: Vendor management/ RM,PM,CAPEX,/Documentation/Market Analysis – Manager Any Graduate | 08–15 yrs 7. PDC(Packaging Development Cell): Review & Approved Artwork/Product packaging/cGMP/DGFT Guideline/Change control/Vendor Communication/Master Packaging card Preparation- Officer to Sr. Executive. B.sc/M.sc/D. Pharm/B.Pharm/Diploma in Packaging Technology| 03–07 yrs 8. Logistic: Pre & Post Documentation | Preparing Export Invoice | Tracking Shipment | Coordination with CHA - Officer to Sr. Executive Any Graduate| 01–05 yrs 9.PPMC: Production Scheduling | Material Requirement Planning | Inventory Management | Demand Forecasting - Officer Any Graduate| 01–02 yrs Contact Us: +91 8511849377 | +91 7486829377 career@opeshealthcare.com Let your career thrive with Opes Healthcare Employee Benefits: Employee Health Insurance| Employee Accidental Insurance|2nd & 4th Saturday Off| Attractive HR Policies| AC- Transportation Facility. Be a part of something impactful. See you at the interview!

To prepare and issue SOPs. BMR / BPR verification. Verification of Rejected Material in Stores. To check calibration status of production instruments/ equipments periodically. To perform the in process analysis. Required Candidate profile To give line clearance during product change over. To supervise the dispensing of raw materials. To organize and collect the ln process, intermediate and Finished Product samples during Manufacturing.

Exciting Career Opportunity at Hetero (Annora Pharma) Pvt Ltd! We are conducting a MEGA Walk-in Drive @GOA for our Formulation Units in Hyderabad. If youre looking to grow your career in the pharmaceutical industry, dont miss this chance to join one of India’s leading pharma companies! Open Positions: 1. Production • Qualification: ITI / Diploma / B.Sc / B. Tech / B Pharm • Experience: 1–6 years • Designation: Operator / Jr. Officer / Officer / Jr. Executive / Executive • Areas: Granulation, Compression, Coating, FBP, QMS, Capsule filling 2. Quality Control • Qualification: M Pharm / B Pharm / MSc • Experience: 1–6 years • Designation: Jr. Officer / Officer / Jr. Executive / Executive • Areas: Stability, HPLC, GC, Wet Analysis, IP/FP, RM, LIMS, Microbiology 3. Quality Assurance • Qualification: M Pharm / B Pharm / MSc • Experience: 1–6 years • Designation: Jr. Officer / Officer / Jr. Executive / Executive • Areas: IPQA, QMS, Market Complaints, AQA, Qualifications, APQR Walk-in Interview Details: Date 1: 24th May 2025 (Saturday) Venue: The Fern Kesarval Hotel & Spa, Verna, Goa Date 2: 25th May 2025 (Sunday) Venue: Boshan Hotels, Mapusa, Goa Job Location: Hyderabad Timings: 09:30 A.M. to 04:30 P.M. Please Bring: • Updated Resume • Education Documents • Last 3 Months’ Payslips • Appointment Letters, CTC Breakup, ID Proof (Aadhar/PAN) For more info, contact: chandrasekhar.r@hetero.com | pavani.ar@hetero.com Cell 9010203989 We look forward to seeing you there!

Raw material, in process & finished goods inspection, 8D report, IATF Handling Customer complaints, Audits, documentation Product Knowledge: UL Cables, special Cables, fire survival cables, Control & instrumentation cables up to 33 KV Team Size: 20 Required Candidate profile B. Tech/ B.E. Electrical/Electronics/Mechanical 10+ years' experience in an electrical cable mfg. co. in quality Significant experience in a managerial capacity Knowledge of IS-694, IS-7098 standards

Job Overview The incumbent will be responsible to ensure that all external and internal processes and systems are followed before our product reaches our customers. You will be responsible for inspecting procedures and outputs and identifying mistakes or non-conformity issues. Qualification: B. Sc. / B. Pharm + M. Sc. /M. Pharm Experience: • 8 to 12 years in Quality Assurance • Thorough knowledge of methodologies of quality assurance and standards • Maintaining cGMP quality standards, ensuring stringent adherence to quality standards, norms & practices, identifying gaps & taking corrective actions. • Excellent numerical, communication skills and understanding of data analysis/statistical methods • Attention to details and Stake Holder management Roles & Responsibilities Process Documentation & Review • Ensure and review adherence to the processes and product quality through site documentation review -BMR/BPR -APQR -Monthly reports -IPQC data -Stability data - Validation Protocol/ Report • Preparing QA SOPs as applicable for TP sites and PEL CPD business and their effective implementation • To design, implement and ensure adherence to Quality Technical Agreement at Third Party Level • Review of Specifications and STPs applicable for Contract manufacturing sites. • Batch release, Ensuring timely analysis of batches and quality of products. • Review of Change control and Deviation at TP sites. • Handling Market complaints and carry out investigation and review, to find out the root cause for the complaint. • Handling of OOS results at contract manufacturing sites and carry out investigation to find out the root cause for the OOS observed. • Departmental SOPs preparation, implementation and Training of SOPs at Head Office. • Review of Specifications and STPs applicable for Contract manufacturing sites. • Review of Annual Product Quality Review of contract manufacturing products and improvement based on the identified Gaps. Process, System and Product Maintenance & Upgradation • Experience in quality standards and regulatory compliance: Implementation of quality system inline with current regulatory requirements. Ability to handle strategic planning by ensuring CMO governance, Gap analysis and risk mitigation documentation, product quality complaints investigation and recall handling. • Ensures Corrective and Preventive Actions (CAPAs) are implemented by CMOs and every task is performed in accordance with established SOPs • Training need identification and imparting Trainings at Contract manufacturing sites. • To upgrade quality system by ensuring tracking systems to monitor timelines and effective compliance to planned system. • Experience in Handling Technology Transfer (Analytical/ Process): Facilitate in transferring registration and relevant Quality document to CMO & ensure proper documentation of the transfer as per quality requirements

Why Join Siemens? At Siemens, you will be part of a global leader committed to innovation, quality, and excellence. This role offers the opportunity to work on challenging projects, develop professionally, and make a significant impact in the electrical and instrumentation domain, particularly within power plant and renewable energy projects. If you are passionate about leading a talented team and driving technical excellence, we encourage you to apply. As Siemens Energy, "We energize society" by supporting our customers to make the transition to a more sustainable world, based on innovative technologies and our ability to turn ideas into reality. We do this by Expanding renewables Transforming conventional power Strengthening electrical grids Driving industrial decarbonization Securing the supply chain and necessary minerals Looking for a challenging role? If you really want to make a difference - make it with us Job Requirements The candidate will be responsible for reviewing engineering drawing thoroughly from design, manufacturing and site operation point of view. Evaluation of engineering drawing from factory machining facility perspective. Identify in-house or vendor level component machining challenges during project execution. Evaluation of engineering drawing from factory assembly perspective. Identify any assembly challenges during project execution and new product development. Evaluation of complete project based of site execution challenges and operational philosophies for different product fleet lines. Experience of machining, assembly and site execution is a critical aspect for this role in addition to basic design knowledge. We"™ve got quite a lot to offer. How about you? This role is based in Vadodara, where you"™ll get the chance to work with teams impacting entire cities, countries and the shape of things to come. We"™re Siemens. A collection of over 379,000 minds building the future, one day at a time in over 200 countries. We're dedicated to equality, and we welcome applications that reflect the diversity of the communities we work in. All employment decisions at Siemens are based on qualifications, merit and business need. Bring your curiosity and imagination and help us shape tomorrow.

Roles and Responsibilities Ensure compliance with GMP guidelines, BMRs, OSD requirements, and WHO standards for IPQA activities. Develop and implement effective quality control processes to ensure product quality and regulatory compliance. Conduct regular audits, inspections, and investigations to identify areas of improvement in batch manufacturing operations. Collaborate with cross-functional teams to resolve quality issues related to formulations, tablets, capsules, etc. Provide training on Good Manufacturing Practices (GMP) and other relevant regulations to employees.

Position: R&D OFFICER Education: BSc. in chemistry, MSc. in chemistry or B.pharma / M.Pharma Experience: minimum 10 year in API pharmaceutical industries. Salary: 50 to 70 K per month Mo No : +91 90816 99400 / +91 90816 88100 / 90816 99600 Required Candidate profile Coordinate with regulatory authorities for inspections, licensing, and compliance documentation. Investigate quality incidents, deviations, and complaints, ensuring timely resolutions

Job Category: Quality Engineer Experience: 3+ Yrs Primary Responsibilities Reports to the Manager Quality. Responsible for inspection and qualification of all the BOM items, create and maintain necessary reports. Suppliers performance Reports monitoring, benchmarking and conduct process audits. Train the supplier to reach Invendis Quality goals. Responsible for inspection process efficiency. Responsible for inspecting all the in-process stages as per the quality requirements and compliance. Effective monitoring and control of daily yield. Conduct audits (Process audit, Internal Audit, etc.,) including closing out audit findings, creating audits finding reports and determine proper corrective and preventive actions. Perform Investigation, Root cause analysis, corrective action for regular production/customer complaint. Assess and pro-actively improve process yield. Develop new testing plan for a product as per customer compliance (Product basis) & implementation in the operation as per QA target. Ensure testing methodology, techniques, standards are developed & established with supporting lab equipment facilities. Preparation of verification, validation of test plans, test procedures and test reports. Maintenance of automated test environment, perform unit, functional and Final testing for running products. Maintenance of calibration reports of the equipment s and renewal of lab facilities as per schedule. Responsible for self-funding of the laboratory Responsible for shipment clearance Skills & Competencies Required IQC Incoming Quality Control IPQA -In-Process Quality Assurance FQA -Factory Quality Assessment OBA Out-of-box Audit Education Qualification & Work Experience ITI/DIPLOMA/B.E 3+Year - Quality engineer Touch Points Production Team SCM Supplier