311 Oot Jobs - Page 7

Handling of QMS System (Change Control, deviations, OOS, OOT, CAPA, etc.) Validation Activities Aware of Equipment / Instruments qualifications Good Knowledge of SOP preparation & Review Good Knowledge of APQR Aware of Internal Audit Activities

1-Lead QA/QC team,2-Implementation of QMS,3-implementation of good housekeeping, Safety in QC.4-Review & approval STP,SOP, Calibration record, CAPA, Audit compliance, Handling Training,Co-ordination with Production Warehouse,Quality Coordination.

1-Lead QA team,2-Implementation of QMS,3-implementation of good housekeeping, Safety .4-Review & approval STP,SOP, Calibration record, CAPA, Audit compliance, Handling Training,Co-ordination with Production Warehouse,Quality Coordination.

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...

To ensure and carry out the analysis of sample and all other activities as per Standard Operating Procedure (SOP). To follow and ensure Good Laboratory Practices (GLP), Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) inside lab. To check, verify and review the calibration of all the analysis instruments whether performed as per the schedule. To ensure recording of all the data related to the testing online, on day-to-day basis and ensure traceability of the same. To work for lab readiness for audit and ensure compliance in Laboratory.

To ensure and carry out the analysis of stability sample and all other activities as per Standard Operating Procedure (SOP). To get involve and support in investigation of failure of any material or product in case of any out of specification (OOS) or Out of trend (OOT) or laboratory incident or non-conformity and take corrective and preventive actions. To raise and implement change control or document change request wherever necessary. To follow and ensure Good Laboratory Practices (GLP), Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) inside Stability lab. To ensure availability of the working & impurities standards as per various pharmacopoeia. To assist Supervis...

To ensure and carry out the analysis of stability sample and all other activities as per Standard Operating Procedure (SOP). To get involve and support in investigation of failure of any material or product in case of any out of specification (OOS) or Out of trend (OOT) or laboratory incident or non-conformity and take corrective and preventive actions. To raise and implement change control or document change request wherever necessary. To follow and ensure Good Laboratory Practices (GLP), Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) inside Stability lab. To ensure availability of the working & impurities standards as per various pharmacopoeia. To assist Supervis...

Greetings from MSN Laboratories...! We are conducting a walk-in interview for Experienced candidates in Our APICHEM Unit Vangapalli (Near to Yadagirigutta) on 27th Sept 2025 (Saturday). Department- Quality Assurance- AQA& QMS Req Exp- 3 to 8 Yrs Qualification- B. Sc Chemistry/ Any Graduate Designations- Executive/ Jr. Executive/ Sr. Executive Department- TSD Req Exp- 03 TO 08 Yrs Qualification- B. Tech Chemical Designations- Executive/ Jr. Executive/ Sr. Executive Venue Details- APICHEM Laboratories Pvt. Ltd, Vangapalli (V), Yadagirigutta (M), Yadadri Bhuvangiri (D), Telangana. Date- 27th Sept 2025 (Saturday)

Walk-In Interview Date : 25th, 26th & 27th September 2025 (Thursday , Friday & Saturday) Timing : 9:00 AM to 4:00 PM Venue : Umedica Laboratories Pvt, Ltd. Plot No 221,221/1 II Phase GIDC Nr Morarji Circle, Vapi 396195. 1. Tablet Manufacturing Department: Ability to handle process like Dispensing, Granulation, Compression, Coating, SOPs preparation, well versed with ALCOA & GDP principles. QMS Manufacturing investigation (OOS/OOT/Deviation/CAPA),Training.) Position: Officer to Executive Qualification: M.Sc. / B.Pharm / M.Pharm No. of Vacant Position: 20 Experience: 2 to 8 years To Operate Granulation lines (RMG/FBD/FBP/Roll Compactor), Automatic Compression Machine (PLC/SCADA based Cadmach &...

About Company Founded in 2011, ReNew, is one of the largest renewable energy companies globally, with a leadership position in India. Listed on Nasdaq under the ticker RNW, ReNew develops, builds, owns, and operates utility-scale wind energy projects, utility-scale solar energy projects, utility-scale firm power projects, and distributed solar energy projects. In addition to being a major independent power producer in India, ReNew is evolving to become an end-to-end decarbonization partner providing solutions in a just and inclusive manner in the areas of clean energy, green hydrogen, value-added energy offerings through digitalisation, storage, and carbon markets that increasingly are integ...

Role & responsibilities Sampling and analysis of Raw Materials, In-process samples, Finished Products , and Stability samples as per SOP and test methods. Preparation and standardization of volumetric solutions, reagents , and reference standards . Performing routine chemical, instrumental (HPLC, GC, UV, FTIR), and microbiological testing (for applicable roles). Equipment/instrument calibration and maintenance logs. Participation in method validation , stability studies, and process validation activities. Adherence to Good Laboratory Practices (GLP) and regulatory standards. Supporting internal and external regulatory audits (like USFDA, WHO-GMP). Reporting deviations, OOS results, and non-c...

Roles and Responsibilities Conduct stability analysis, method validation, and OOS investigations to ensure product quality. Ensure compliance with regulatory requirements by maintaining accurate records and documentation. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Perform HPLC, GC, FP, and OSD testing as per SOPs.

Job Alert Sr. GM / Associate Vice President – Quality Control Location: North India Industry: API / Chemicals Manufacturing Salary: Open (Attractive hike on current package) Experience: 16+ Years | Age: 50 Years We are seeking a dynamic Quality Control leader for a reputed API Manufacturing organization . The candidate must have strong exposure to regulatory-driven companies with proven expertise in leading global regulatory audits (USFDA, EMA, MHRA, etc.) and managing large QC operations. Key Responsibilities: Head the Quality Control department ensuring compliance with cGMP & international regulatory guidelines. Lead a QC team of 150–200 employees , driving efficiency, compliance, and tech...

To ensure the GMP and GLP compliances. To participate in OOS, OOT, Deviation and complaint investigation, root cause analysis and to review investigation report. To carry out closure activities. To compile data provided by manufacturing, warehouse, QC for preparation of complaint investigation report. To prepare and review trends of OOS, OOT, Deviation, complaints, customer audit/inspection. To initiate change controls pertaining to QA and to review change controls of other departments w.r.t impacted activities. To review change control trend. To compile data for and prepare, review risk assessment reports w.r.t. Deviation, OOS, OOT, Nitrosamine impurities, elemental impurities, etc. To appr...

Role & responsibilities Suggested position: Sr Manager / Manager Education: Post Graduation (Life sciences preferred) Total Exp: 15-17 Years (Biopharma is preferred) Others: Ready to support in different shifts Responsibilities: Mainly responsible to review of Harvest, Drug Substance and Drug Product analytical (Biosimilars) raw data and analytical trends Conduct Gemba walkthroughs in QC department and to ensure quality compliance. Involve in investigations (Deviations, OOS, OOT, Lab incidents) to ensure QMS compliance for QC sections Audit trails and conduct routine monitoring in QC to check effectiveness of the system implemented. Responsible for preparation and review of documents SOPs, P...

Manage release of product batches, including owning the QA product release workflow in SAP. Lead and supervise a team of QA professionals to perform operations as described above. Review and approve Purchase Specifications

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.

Manage release of product batches, including owning the QA product release workflow in SAP. Lead and supervise a team of QA professionals to perform operations as described above. Review and approve Purchase Specifications

TECHNICAL AND JOB SPECIFIC: Review of Technical Design Documents and Unit Test documents. Preparation and review of calibration, Preventive Maintenance, Breakdown SOPs . Handling of deviations, change control, CAPA, OOS/OOT investigations. Knowledge of qualification and calibration of instruments/equipments. Knowledge on creation of Equipment Functional Location, Bill of Materials, Work Centers, classes and characteristic, measurement points, Task List, Maintenance Plans, Warranties, Knowledge on work order management, Preventive Maintenance, Calibration Management, Breakdown Maintenance, Revalidation, Mapping, Refurbishment process, Inventory Management, Master Data Management( Creation and...

TECHNICAL AND JOB SPECIFIC: Review of Technical Design Documents and Unit Test documents. Preparation and review of calibration, Preventive Maintenance, Breakdown SOPs . Handling of deviations, change control, CAPA, OOS/OOT investigations. Knowledge of qualification and calibration of instruments/equipments. Knowledge on creation of Equipment Functional Location, Bill of Materials, Work Centers, classes and characteristic, measurement points, Task List, Maintenance Plans, Warranties, Knowledge on work order management, Preventive Maintenance, Calibration Management, Breakdown Maintenance, Revalidation, Mapping, Refurbishment process, Inventory Management, Master Data Management( Creation and...

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...

QMS Documentation: Handling change control, deviation, CAPA (Corrective & Preventive Actions), complaints, OOS (Out of Specification), OOT (Out of Trend), etc. Audits & Compliance: Risk Assessment: Product Quality Review (PQR)