253 Cleaning Validation Jobs - Page 5

Vibonum Technologies Private Limited, a part of the esteemed Althera Group, is conducting a Walk-in Interview to hire Production Manufacturing, Packing and Warehouse Dispensing professionals for its state-of-the-art OSD manufacturing facility in Nanjangud, Mysore . Interview Date: September 27th 2025 Time: 09.00 am to 05.00 pm Venue: Hotel Kinara Residency # 2-1, S R Chambers, Beside BSNL Building, Chandannagar, Hyderabad - 500050 --------------------------------------------------------------------------------------------------------- Open Positions: Assistant Manager- Production (Exp- 8-10 yrs ) Sr. Executive production Mfg. / Production pkg . (Exp- 5-8 yrs ) Executive production / Packing ...

Job Description: Ensure GMP compliance. Issue formats & protocols for Process Validation and Hold Time Study. Prepare protocols and reports for Process Validation & Hold Time Study; compile related data. Maintain all process validation documents along with batch records. Perform Process Validation activities on the shop floor. Maintain qualification records as per requirements. Execute equipment software and system qualification & re-qualification activities under supervision and coordination with concerned departments. Prepare QA SOPs. Ensure discipline within the department. Handle incidents, deviations, change controls, and CAPA. Prepare, review, and approve Cleaning Validation Matrix. Pr...

Vibonum Technologies Private Limited, a part of the esteemed Althera Group, is conducting a Walk-in Interview to hire Quality Control professionals for its state-of-the-art OSD manufacturing facility in Nanjangud, Mysore . Department: Quality Control Work Location: OSD Plant, Nanjangud, Mysore Interview Date: September 28th 2025 Time: 09.00 am to 05.00 pm Venue: Hotel Kinara Residency # 2-1, S R Chambers, Beside BSNL Building, Chandannagar, Hyderabad - 500050 20 Open Positions: Assistant Manager / Sr. Executive / Executive / Sr. Officer Eligibility: Education: B. Pharm / M. Pharm / M. Sc Exp: 6-8 Years ------------------------------------------------------------------------------------ Job R...

To perform microbiological testing of raw materials, in-process samples, finished products, water, and environmental monitoring to ensure compliance with regulatory and company standards. Required Candidate profile Requirements: Microbiology testing / analysis work Skills: MS Office, Communication Skills

As a Computer System Validation & QA-IT professional, your role involves various responsibilities related to process activities. Some of the key responsibilities include: - Reviewing Qualification and Re-Qualification protocols & reports. - Reviewing Preventive Maintenance & Calibration records. - Reviewing and approving critical consumable items. - Monitoring engineering & utility services such as facility layouts, building layout, material flow, HVACs, Nitrogen plant generation and distribution, purified water generation and distribution, and Equipment qualification. - Reviewing breakdown maintenance system. - Handling SAP activities for Engineering. - Managing new product introduction at ...

Roles and Responsibilities Execute equipment qualification, validation, cleaning validation, vendor qualification activities according to SOPs and regulatory requirements. Conduct process validation protocols, reports preparation, and review of documents. Ensure compliance with cGMP guidelines during execution of QA activities. Collaborate with cross-functional teams to resolve issues related to QA operations. Maintain accurate records of all QA activities and documentation.

Design and execute validation protocols for process and cleaning validation activities, including IQ (Installation Qualification), OQ (Operational Qualification), PQ (Performance Qualification), and CV (Cleaning Validation). Develop and maintain a validation master plan (VMP) that aligns with regulatory requirements and organizational goals. Conduct process validation studies to ensure manufacturing processes consistently produce products that meet predefined quality attributes. Analyze process performance and critical parameters during validation runs and document results. Ensure adherence to Good Manufacturing Practices (GMP) during all validation activities. Develop and execute cleaning v...

As a responsible team member in the pharmaceutical manufacturing process, your role involves the following key responsibilities: - Conduct line clearance activities before starting various operations such as dispensing, manufacturing, filling, inspection, sealing, labeling, and packing. - Perform process validation, cleaning validation/verification, hold time study, media fill, and routine batch sampling according to protocol/SOP. - Review executed Batch Manufacturing Records (BMRs) and Batch Packaging Records (BPRs). - Perform in-process tests at different stages as per batch documents/SOP. - Review environmental monitoring and water trends. - Review different types of calibration certifica...

About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions. For more information visit: www.apotex.com . Job Summary A role-holder to handle/supervise the manufacturing activities and to ensure t...

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...

About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions. For more information visit: www.apotex.com. Job Summary A role-holder to handle/supervise the manufacturing activities and to ensure th...

Role & responsibilities Executive - QA Equipment Qualification Preferred candidate profile - Review of Equipment Qualification related documentation. - Review of Computer system validation related documentation. - Exposure of Software like EDMS, LMS, Trackwise. - Exposure of Cleaning validation.

Job Title: Sr. Executive Location: Bavla - Plant Department: QA Reporting To: Head of QA Employment Type: Full-Time Key Responsibilities: Prepare and review Cleaning Validation Protocols and Reports , including product matrix and MACO (Maximum Allowable Carry Over) calculations. Develop and execute protocols and reports for Clean Equipment Hold Time and Dirty Equipment Hold Time . Prepare, review, and finalize Process Validation Protocols and summary reports, utilizing analytical results and batch documentation data. Prepare and review Product Hold Time Protocols and Reports to ensure product quality throughout storage. Conduct thorough review of manufacturing documentation, including Master...

Role Overview: As a Manager in the Quality Assurance department at ZLL-SEZ Oncology Injectable (Alidac), your role will be critical in handling in-process Quality Assurance functions. You will ensure that defined and approved IPQA checks are followed and documented during Dispensing, Manufacturing, filling, capping, and Packing stages. Your responsibilities will include ensuring compliance with Current Good Manufacturing Practices and sterility assurance activities in aseptic product manufacturing. Additionally, you will review Smoke study protocol, report, and Video recording, and participate in regulatory audits. Key Responsibilities: - Handle in-process Quality Assurance functions by ensu...

Conduct quality inspections and tests on raw materials, in-process production, and finished products.Monitor and document quality control processes and compliance with quality standards.Identify defects or deviations

Conduct regular inspections and audits of products, processes, and systems.Identify quality issues and implement corrective actions.Develop and maintain quality documentation, including SOPs and checklists.

Conduct regular inspections and audits of products, processes, and systems.Identify quality issues and implement corrective actions.Develop and maintain quality documentation, including SOPs and checklists.

Key Responsibilities Lead, manage, and develop the QC function for pharma formulations as per company policies and regulatory requirements. Supervise and resolve lab incidents, deviations, change controls, OOS/OOT , and ensure robust documentation and root cause analysis. Oversee process validation, cleaning validation, hold time studies and related compliance activities. Establish and implement Stability Study protocols as per company SOPs, client specification, and all applicable quality standards. Handle product complaints & recall investigations in collaboration with QA and Production teams. Ensure compliance with current GMP, GLP, and regulatory guidelines for all laboratory operations....

Role & responsibilities Monitoring and continuously up keeping food safety and hygiene standards of the kitchen Giving training to the kitchen team on various SOPs, quality and food safety standards Prepping kitchen to comply to FSSAI standards and other internal audits Proactively checking the quality of raw ingredients/products through sensory and its documentation Handling customer complaints by doing RCA and sharing CAPA Analyzing data to understand regional performance on various metrics Ready to travel to different locations of the city Key Competencies Good communication skills Good understanding of the domain of food safety, RCA & CAPA , quality standards Well versed with FSSAI regul...

Summary Job Functions: Responsible for document review (Ex. Master MPCR/BPCR, QMS documents, SOP, Protocols & Reports) related to BBM, MSAT & R&D. Responsible for IPQA activities and Shop Floor Compliance in BBM Facility. Responsible for transactions required in software related to GMP activities Key Responsibilities: - Responsible for In-Process Quality Assurance activities (e.g. Area clearance, Issuance of MCB/ WCB/ EPCB Vial/ CI/ DS for batch processing, Verification of process steps as applicable and review of various processing parameters and its associated documentation related to BBM facility. - Review of new & revised documents and related transactions in respective software. (SOP, E...

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...

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...

Job Description Join Lupin Limited in the role of Junior Officer within our Quality division, specializing in Validation activities. This position is integral to ensuring the highest standards in cleaning validation processes for Active Pharmaceutical Ingredient (API) facilities. Your primary responsibility will involve managing and executing comprehensive cleaning validation protocols to guarantee product safety and regulatory compliance. Key responsibilities include: Conducting residue cleaning validation to verify the removal of contaminants from manufacturing equipment. Performing nitrosamine cleaning validation to monitor and control genotoxic impurities in line with current global regu...

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...