552 Oos Jobs - Page 9

We are looking for a skilled SAP CRM-C4C professional with 9 to 20 years of experience. The ideal candidate will have expertise in SAP C4C and be able to work effectively in a fast-paced environment. Roles and Responsibility Manage and implement SAP C4C solutions for clients. Collaborate with cross-functional teams to identify business requirements and develop solutions. Provide training and support to end-users on SAP C4C functionality. Troubleshoot and resolve technical issues related to SAP C4C. Develop and maintain documentation of SAP C4C configurations and customizations. Ensure data integrity and security in SAP C4C implementations. Job Requirements Strong knowledge of SAP C4C modules...

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

Requisition for Executive for the implementation and monitoring of GLP in TIC. Skills Required : Good Laboratory Practice, Quality Assurance, MS Office Package, Communication Skills Roles and Responsibilities : Preparation of documents related to applying GLP (Good Laboratory Practices). Ensure the upkeep and maintenance of the laboratory by implementing GLP. Ensure compliance with GLP standards. Logbook management, sample management, SOP management, and other document management related to GLP. Any other work related to Quality assurance assigned by the manager. GLP-trained person or experience working in GLP labs. Must have good verbal and written skills.

Key Responsibilities: Manage all Analytical Quality Assurance (AQA) activities. Review, approve, and close Quality Management System documents related to QC. Act as Single Point of Contact (SPOC) for submission activities Dossier, Regulatory, Variation filings. Handle customer communications related to QA. Review manufacturing, packing, analytical reports of submission/validation batches. Review Stability data and ensure submission compliance. Ensure compliance of Stability Studies and Control Sample Handling at site. Ensure adherence to GDP/GLP. Monitor compliance of Gowning/De-gowning in QC lab. Authorize written procedures, amendments, and related documentation. Ensure SOP compliance acro...

We are looking for a skilled professional with 6-15 years of experience to join our team as an Allegro QA/Developer in PAN India, including Bangalore, Hyderabad, Pune, Chennai, and Noida. The ideal candidate will have expertise in designing Allegro-based functional prototypes and functional modeling of business flows. Roles and Responsibility Design and develop Allegro-based functional prototypes and models. Document functional design, data design, and setup in Allegro. Collaborate with cross-functional teams to identify and prioritize project requirements. Develop and maintain high-quality code using Allegro. Troubleshoot and resolve technical issues related to Allegro. Participate in code ...

About The Role Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : IT Infrastructure Operations Good to have skills : NA Minimum 5 year of experience is required Educational Qualification : 15 years full time education Position Summary The IT Infrastructure Architect will design, implement, and optimize enterprise-level solutions across Operating Systems, Databases, Site Reliability Engineering (SRE), and Middleware platforms. The role requires deep technical expertise, strategic planning, and leadership to ensure high availability, scalability, performance, and secu...

Skills Required: Graduate / PG in management With a minimum of 4-7 years of experience in managing the Admin function. Must have hands on experience into Advance Excel Key Responsibilities Making MIS Reports of collated data Meticulously working on the data collated from various sources of department and preparing comprehensive reports Ensuring the precision of the reports Preparing Delivery Files Extensive work on Excel Preparing necessary dashboards for day to day operations Monitor & analyses data for business trends & prepare monthly revenue & collection report Provide cross functional quality oversight from a compliance perspective fo testing and disposition, quality investigations, val...

Roles and Responsibility Conduct thorough reviews of patient data to ensure accuracy and compliance with regulatory standards. Analyze complex data sets to identify trends and patterns that inform business decisions. Develop and implement effective data visualization techniques to communicate insights to stakeholders. Collaborate with cross-functional teams to design and implement process improvements. Provide expert guidance on data management best practices to junior team members. Stay up-to-date with industry developments and emerging trends in health data analytics. Job Requirements Strong understanding of healthcare operations and regulations. Proficiency in data analysis and visualizat...

Roles and Responsibility Review electronic case report forms (ECRF) data for accuracy and completeness. Identify and resolve discrepancies or errors in ECRF data. Collaborate with cross-functional teams to ensure data quality and integrity. Develop and implement processes to improve ECRF data review efficiency. Provide feedback on data quality issues to stakeholders. Participate in ongoing training and professional development to enhance skills and knowledge. Job Requirements Strong understanding of ECRF data review principles and practices. Proficient in using relevant software applications and tools. Excellent analytical and problem-solving skills with attention to detail. Effective commun...

Role & responsibilities -Handling of Pharma Instruments i.e. HPLC, GC, UV, KF, IR, etc. -SOP Preparation. -Analytical documents preparation. -Wet analysis to be performed. Preferred candidate profile -Having experience in Pharma company only. -Having experience to face regulatory & customer audits. -Having knowledge of GLP & GMP importance.

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.

As a Scientist at Novartis, you will be responsible for planning and performing scientific experiments for the timely delivery of drug substances, drug products, processes, and procedures within a multifunctional project team. Your role will involve collaborating with a Project Leader and contributing to the maintenance of lab instruments and infrastructure. Key Responsibilities: - Meet quality, quantity, and timelines in all assigned projects - Perform and document scientific experiments - Plan and organize scientific experiments with minimal guidance - Provide documentation of raw data and evaluate results - Propose and provide input for the design of next experiments - Generate lab proced...

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...

About The Role Job Title - Internal Audit Analyst Management Level :11 Analyst Location:Bangalore Must have skills: Chartered Accountant with 2 - 3 years of post-qualification experience in external or internal auditing, preferably in Big 4 or a global organization. Good to have skills: Internal Audit experience with Big 4 or a global organization Job Summary : An agile, highly motivated, innovative thinker with a background in audit, risk, or compliance looking to join a fast-paced, global Internal Audit department that has embraced transformative capabilities including advanced analytics, dynamic risk assessment, and automation to retain its role as a trusted advisor to the business. You a...

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.

We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job you will find purpose and pride. To ensure the implementation and maintenance of Current Good Manufacturing Practice (cGMP) standards and all To enumerate and report the tubes and plates and to supervise the discarding method of the same. To perform periodic microbiological tests, as per Standard Operating Procedure (SOP). To perform the Bacterial Endotoxin Test. To test the material for their pre-sterile bio-burden and to test Raw Material (RM)/ Packing Material (PM) for bio-burden test. To co-ordinate with Technical department for...

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...

Role Overview: You will be responsible for initiating, reviewing, and approving various quality management systems such as Change Controls, Deviations, Investigations, CAPA, OOS, and Complaints. In addition, you will handle Return Goods and ensure the proper functioning of the quality system by performing risk assessments as needed. Conducting regular internal audits will also be part of your duties. Key Responsibilities: - Review and approve all documents including SOPs, Spec & STPs, Forms, protocols, and reports to ensure compliance. - Review annual product quality review reports and provide training on cGMP topics to employees at the site. - Support customer audits/visits and regulatory a...

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...