64 Quality Operations Jobs

Handle market complaints received from across the globe. You will be responsible for reviewing the investigation reports received from the Novartis sites and Contract Manufacturing Organizations. You will collaborate with external Supply organization, Novartis sites, Country pharma organizations for continuous improvement. As a Specialist - Product Complaints - QOP based in Hyderabad, your key responsibilities will include performing day-to-day activities of processing market complaints assigned as per the relevant SOPs, business matrix, and SLA timelines. You will assist in data collection and reporting of KPIs, participate in continuous improvement initiatives, manage ad-hoc projects, and proactively report all deviations through timely escalations. Your role will also involve implementing continuous process improvement projects to enhance quality & productivity, ensuring that the service dashboard, order management framework, and time sheet are always kept updated. You will receive training on relevant procedures before taking up any GxP activities and report deliverable status while continuously acquiring process knowledge. The essential requirements for this role include having 5-8 years of relevant experience in Quality Operations, a thorough understanding of Quality Management Systems, and the ability to review market complaints investigation reports. You should have a basic understanding of product manufacturing, Pharma products and lifecycle events, Trackwise, performance KPIs, MS Excel, and awareness of GXP. Strong communication skills are essential, with fluency in verbal and written English; knowledge of other languages is an added advantage. A graduate or post-graduate degree in Pharmacy would be a desirable requirement for this position. Novartis is committed to building an outstanding, inclusive work environment with diverse teams representative of the patients and communities served. If you are looking to be part of a mission to reimagine medicine and improve lives, consider joining Novartis. To learn more about the benefits and rewards offered at Novartis, please refer to the Novartis Life Handbook. If this role does not align with your current experience or career goals, you can stay connected and learn about other career opportunities within Novartis by joining the Novartis Network. Novartis values the contribution of its associates in driving the company towards becoming the most valued and trusted medicines company in the world.,

Strong expertise in chemical plant operations, safety, project execution.Complete site operations including Production planning, Maintenance, Quality, Projects, resource allocation for the site. Leadership for technology transfer & implementation. Required Candidate profile Strong expertise in chemical plant operations, safety, project execution.Complete site operations including Production planning, Maintenance, Quality, Projects, resource allocation for the site.

Job Purpose and Impact The Operations Buyer will apply deep knowledge of local practices and procedures to handle, organize and coordinate procurement of materials, goods, services and supplies. In this role, you will conduct activities focused on transporting products from suppliers to customers and conduct activities to support complex customer issues and operations quality and improvement. Key Accountabilities Creating purchase orders based on contracts or PO request emails, and written communication when necessary, inChinese. Assist more senior team members with process improvements. Check records and files for accuracy, performing complex analysis of data. Lead requests for procurement of non-contracted materials and goods, services and supplies. Assist end user and ensure material delivery follow plant requirements. Handle complex clerical, administrative, technical or customer support issues under minimal supervision, while escalating only the most complex issues to appropriate staff. Other duties as assigned Qualifications Minimum Qualifications Bachelor's degree in a related field or equivalent experience Should have Chinese B2 proficiency Proficiency in Excel is particularly important. Preferred Qualifications Experience with SAP would be an advantage. Advanced skills using relevant office programs and applications Working knowledge of enterprise resource planning application experience Experience working in shared service operations

Support daily quality operations such as inspection and handling of products. Execute incoming inspections for parts and/or raw material, according to given standards. Perform prescribed check routines of different kind and pack parts or products for internal or outward shipping. Release deliveries or products and services which meet expectations, if required. Document results of inspection in the respective IT systems, if required. Report any discrepancies or non-conformities found during inspections to the relevant department. Your Qualifications w/o Formal Education in Technical 1 to 3 years

Schaeffler is a dynamic global technology company with a rich history of private ownership and an entrepreneurial spirit. As a partner to major automobile manufacturers, aerospace, and industrial sectors, we provide numerous development opportunities for you. Your key responsibilities will include supporting daily quality operations by inspecting and handling products, conducting incoming inspections for parts or raw materials, performing check routines, and packaging parts for shipping. You will release deliveries that meet expectations and document inspection results in IT systems. Additionally, you will be responsible for reporting any discrepancies or non-conformities found during inspections. To qualify for this role, you do not need formal technical education but should have 1 to 3 years of relevant experience. At Schaeffler, we value diversity and strive to create an inclusive environment where all ideas and perspectives are respected. We believe that by embracing our differences, we can foster creativity and drive innovation, ultimately contributing to sustainable value creation for our stakeholders and society as a whole. Exciting assignments and exceptional development opportunities await you at Schaeffler, where we are shaping the future through innovation. We are eager to receive your application. For more information and to apply, please visit www.schaeffler.com/careers. Contact Information: Schaeffler India Ltd. Yogesh Sawarkar Phone: +912656602076 For any technical questions, please reach out to technical-recruiting-support-AP@schaeffler.com. Keywords: Experienced, Operator, Full-Time, Unlimited, Quality,

Etraveli Group is the globally leading company for tech solutions and fulfillment capabilities for online sales of flights. We are here to solve complexity, by connecting millions of flights and travelers across the globe, from search and selection to trip and beyond. We hold consumer online travel agency brands like Mytrip, Gotogate & Flightnetwork and serve Booking.com with flights. Etraveli Group has also established strategic partnerships with companies like Skyscanner, Google Flights, TUI, etc. Every day we strive to make the world smaller for our customers and bigger for our people. Our diverse team of more than 2600 passionate professionals is what makes us the industry s tech wonder and the best in the world at what we do. Major offices in Sweden (HQ), Canada, Greece, India, Poland and Uruguay. Location: Mumbai / Pune About the role: Responsibilities Training Delivery: Conduct engaging and effective training sessions on all schedule change policies, procedures, and relevant systems for new hires and existing agents. Content Development: Develop, update, and maintain training materials, job aids, and resources specific to schedule change processes. Knowledge Transfer: Ensure trainees fully understand complex schedule change scenarios, including rebooking, cancellations, involuntary changes, and compensation policies. Performance Coaching: Assess trainee comprehension and practical application of knowledge, providing constructive feedback and one-on-one coaching to improve performance. System Proficiency: Train agents on the effective use of relevant systems (e.g., GDS, internal tools) for processing schedule changes accurately and efficiently. Policy Adherence: Emphasize and ensure adherence to all company policies, airline regulations, and quality standards related to schedule changes. Continuous Improvement: Stay up-to-date with any changes in schedule change policies, system updates, and industry best practices to integrate them into training. Collaboration: Work closely with Operations, Quality Assurance, and other training team members to identify training needs and contribute to overall performance improvement. Minimum 2 years of prior experience in training, coaching, and mentoring roles is highly desirable. Domain Knowledge: In-depth understanding of airline policies, GDS systems (e.g., Amadeus, Sabre, Galileo & NDC porta

You will be responsible for leading a multi-faceted independent quality evaluation process to measure quality across multiple sources and provide insights from the operation. Your role will involve effectively managing and mentoring a team responsible for diverse workflows, Quality channels, and global stakeholders. It will be crucial for you to drive accountability within the teams to meet quality performance goals and ensure program standards are consistently met on a week-over-week basis. Additionally, you will need to assess and prioritize the top-quality issues affecting the teams across all decision-making channels. Collaboration with internal and external stakeholders to build scalable quality systems that enable efficient monitoring of decision accuracy and prompt identification of overall user experience issues will also be a key part of your responsibilities. Your focus will be on driving a proactive outcome and insight environment to continuously improve and deliver an outstanding customer experience across the program. Furthermore, you will be expected to aggregate audit findings, analyze gaps in processes, and identify innovative ways to solve problems upstream, thereby improving customer experience and driving higher efficiency. Your role will involve optimizing program operations with a focus on process management, key strategic initiatives, and bringing forth ideas with tangible actions to enhance business performance. Forecasting and capacity planning to meet business requirements and ensure continuity will also be a part of your responsibilities. In addition, you will proactively share existing bottlenecks and challenges with quantified impact on operations to facilitate appropriate prioritization. Your ability to clearly outline current performance drivers and actions to improve will be crucial in this role. You will also be responsible for managing client communication and leading all business reviews, including WBRs, MBRs, and QBRs. For this role, you should ideally have a minimum of 15 years of diverse experience in a scalable quality operations environment, with a proven track record of managing internal and external stakeholders to drive results. Strong critical and analytical thinking skills, along with an entrepreneurial and proactive mindset, will be essential. Experience with customer outcome and insight focus, excellent collaboration skills, and the ability to adapt to a fast-paced, international work environment will be highly valued. Exceptional communication and presentation skills, fluency in English, effective task prioritization and time management abilities, as well as a proven ability to break down complex processes and identify key pain points for business improvements will be key qualifications for this role. Having a quality certification (e.g., Lean Six Sigma, TQM, etc.) and/or a project management certification (PMP, Prince2, etc.) will be considered a plus for this position.,

Looking for BE/DME engineer with 8-10 years of experience in after sales service of pumps 1) To attend the customer complaints regarding short/wrong supply, issues faced by customer during installation and performance of pumps at site. Provide Technical Guidance to customer & suggest repair techniques. 2) To analyze the complaints and provide solution to the customer with proper root cause analysis 3) Collect application & operation related data for understanding criticalities & possible problems. 4) To share the learnings at site with the concerned stakeholders like operations, quality and purchase team to avoid re-occurrence of the complaints. 5) Gather application & operation related data and various salvaging techniques, used by our customers. 6) Presenting the collected information on claims/ complaints to after sales for work solutions & implement solutions. 7) To prepare case studies for presentation during training. 8) Any other assignment as directed by the superiors from time to time.

Reporting to the Senior Manager International Quality JAPAC, the responsibilities of your role will cover, but are not limited to the following: Main Responsibilities Implement Amgen Quality Management System Identify Continuous Improvement opportunity for Quality Management System Develop Quality Procedures align with Amgen Quality Management System, cGMP requirements, GDP requirements and local regulations Oversight operations of local distributors and stockist to ensure local distributors operations are in compliance with cGMP requirements, GDP requirements, Amgen Quality Management System and Local regulations Act as Quality-related interface with internal and external customers (i.e. : Change control, Non Conformance, Product Complaint, Product Recall, Audit/ Inspection) Support local testing Support BD project and product launches Liaise with internal and external partners to manage day to day operations associated with distribution operations Monitor and ensure on time completion of NC, CAPA, Audit observation, Product complaint and other quality events Develop and Maintain the Quality Agreements with local distributors and partners Develop reports and provide the necessary communications throughout the organizations Develop or review or approve GMP and GDP documents Provide training to distributors and stockiest including distributors/stockist on-boarding training Actively participate on GMP intelligence to review local regulations, standards and guidance related to Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), product testing and Pharmacopoeia requirementsin India. Collaborate with Risk Management and Product Security on handling of counterfeit, product tempering, product theft and product diversion Interact with local regulators as needed. Keep the Senior Manager International Quality - JAPAC informed of the progress of projects and goals and advise on the potential areas of risk/ concern and new developments that may impact the company Support Named Patient Program Supplier Management: Perform quality oversight and audit of key suppliers to Amgen and its subsidiary companies. These suppliers can include API and starting material manufacturers as well as raw materials, devices and finished products suppliers , contract facilities, local laboratories, importers, distributors, logistics service providers, warehouse, etc. Apply advanced knowledge of Indian and global market regulations to assess supply security risks. Work on an active risk management tool etc. to appropriately deploy Quality Systems on oversight of Amgen suppliers; including selection and approval, due diligence assessment, intelligence monitoring, on-site visit/audit and (if needed) Person in Plant placement, etc.. Support in identifying, assessing and addressing supplier s GMP/GDP risks in collaboration with Amgen sites. Execute necessary tasks and projects as assigned by management in timely manner; to attain assigned goals. Provide support for regulatory inspections of key facilities as needed. Win What we expect of you Qualifications Pharmacist Registration in India. Hold a valid practicing certificate as Pharmacist in India. In-depth knowledge and experience of Good Manufacturing Practice (GMP) & Good Distribution Practice (GDP). Experience with Quality Management Systems including but not limited to change control, deviation, validation, complaints, disposition and audits/inspections. Experience with Commercial Quality Operations and third-party management. Experience with distribution models and/or establishment of new entity procedures a plus Thrive What you can expect of us As we work to develop treatments that take care of others, we work to care for our teammates professional and personal growth and well-being. Vast opportunities to learn and move up and across our global organization Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Career Category Regulatory Job Description Let s do this. Let s change the world. In this vital role you will report into the Regulatory Compliance Team lead. The Regulatory Compliance Change Assessor will interface with the Amgen Global, Site, Biosimilars, and/or Device RA CMC teams, as well as Amgen Operations, Quality, and/or Supply Chain for specific strategies or activities that impact a product. The Change Assessor will be responsible for varying levels of product support, including global reportability assessment of single or cross-product changes, based upon their experience level. Roles & Responsibilities: Key responsibilities of the Regulatory Manager include: Reviews change records to evaluate impact of the change with respect to reportability and product restrictions for any product in scope. Defines and documents the reporting and product distribution restriction requirements for the change within the change control management system. Liaise with other functions, including Process Development, Operations, Quality and Supply Chain to ensure alignment of regulatory strategies Provides expertise and guidance to interdepartmental and cross-functional teams Coaches and support junior regulatory staff s career development Identifies and implements process improvements for the change management process What we expect of you We are all different, yet we all use our unique contributions to serve patients. The [vital attribute] professional we seek is a [type of person] with these qualifications. Basic Qualifications: Doctorate degree OR Master s degree and 4 to 6 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry OR Bachelor s degree and 6 to 8 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry OR Diploma and 10 to 12 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry Preferred Qualifications: Degree in Life Science discipline Regulatory CMC specific knowledge & experience Understanding and application of principles, concepts, theories and standards of scientific/technical field Experience in manufacture, testing (QC/QA or clinical), or distribution in Pharmaceutical/Biotech industry What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.

Career Category Regulatory Job Description The Regulatory Compliance Change Assessor will interface with the Amgen Global, Site, Biosimilars, and/or Device RA CMC teams, as well as Amgen Operations, Quality, and/or Supply Chain for specific strategies or activities that impact a product. The Change Assessor will be responsible for varying levels of product support, including global reportability assessment of single or cross-product changes, based upon their experience level. Roles & Responsibilities: Key responsibilities of the Regulatory Sr Associate include: Reviews change records to evaluate impact of the change with respect to reportability and product restrictions for any product in scope. Defines and documents the reporting and product distribution restriction requirements for the change within the change control management system. Liaise with other functions, including Process Development, Operations, Quality and Supply Chain to ensure alignment of regulatory strategies What we expect of you We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a type of person with these qualifications. Basic Qualifications: Master s degree OR Bachelor s degree and 2 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry OR Associate s degree and 6 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry OR Diploma and 8 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry Preferred Qualifications: Degree in Life Science discipline Regulatory CMC specific knowledge & experience Understanding and application of principles, concepts, theories and standards of scientific/technical field Experience in manufacture, testing (QC/QA or clinical), or distribution in Pharmaceutical/Biotech industry .

As a Quality Operations Support at Sandoz, your major accountability is to adhere to the current GxP and compliance requirements while delivering quality operations to ensure product quality compliance and regulatory workflows. You will be responsible for ensuring compliance to Sandoz quality standards, relevant regulatory requirements, filed product quality standards, and service level agreements. Additionally, you will support the implementation of service quality and process improvement projects, as well as CAPA management within GQSI. It is crucial to comply with internal functional requirements, including KPI reporting, ticket management tools, and other internal procedures and processes. Regular communication with customers and partners to collect feedback on support services and report deliverables is a key aspect of your role. Focus on completing all relevant and assigned trainings in a timely manner to enhance your skills and knowledge. As you progress in this role, it is important to learn and develop an understanding to generate insights through data and digital means. Taking responsibility and ownership of assigned tasks, ensuring accuracy, and timeliness of deliverables is essential. You will be required to manage accounts in workflow applications such as SAP, GxQEM, CONDOR, ESOPs, TrackWise, etc., to ensure the appropriate execution of service deliverables. Furthermore, you will generate and analyze predefined and ad-hoc reports in various applications like Trackwise, GxQEM, etc., and take follow-up actions as needed. Joining Sandoz means becoming part of the backbone of the global medicines industry. Sandoz, a leader in generic and biosimilar medicines, has impacted the lives of almost 500 million patients last year. With a commitment to doing more, Sandoz is investing in new development capabilities, state-of-the-art production sites, acquisitions, and partnerships to shape the future and provide more patients with access to low-cost, high-quality medicines sustainably. At Sandoz, you will experience an open, collaborative culture driven by talented and ambitious colleagues. You will have the opportunity to work in an agile and collegiate environment with impactful, flexible-hybrid careers. Diversity is welcomed, and personal growth is encouraged, enabling you to shape the future of Sandoz and make a difference in the lives of patients worldwide. Embrace the momentum and entrepreneurial spirit at Sandoz as we shape the future together.,

Job Summary: The ZED Facilitator is responsible for assisting Micro, Small & Medium Enterprises (MSMEs) in registering for the ZED Certification scheme and supporting them throughout the certification process. The role includes field visits, data collection, documentation support, and ensuring successful completion of ZED Bronze assessments in compliance with the Ministry of MSME s guidelines. Key Responsibilities: Visit MSME units for awareness generation and onboarding them under the ZED scheme. Guide MSMEs in UDYAM and ZED portal registration. Collect relevant data, photographs, and documents required for ZED Certification. Assist units in fulfilling ZED Bronze-level criteria including health, safety, environment, and quality aspects. Upload inspection findings, photos, and reports on the ZED portal. Coordinate with the backend team and State Coordinator for clarification and issue resolution. Ensure NCs (Non-Conformities) are addressed and closed in a timely manner. Maintain proper records of units visited, certified, and pending. Act as the primary point of contact between the MSME and the Organising Partner. Eligibility Criteria: Education: Graduate in any discipline (Science/Engineering/Commerce preferred) Experience: 1-3 years in field surveys, audits, MSME engagement, or government schemes Technical Skills: Basic understanding of MSME operations and quality parameters Familiarity with ZED Certification and sustainability principles Proficiency in smartphone-based data entry, photo/video documentation Desired Competencies: Strong interpersonal and communication skills Ability to work independently and manage field responsibilities Attention to detail in documentation and reporting Willingness to travel extensively within the allocated district/region Remuneration: Performance-based compensation model (e.g., fixed amount per successful certification, typically INR 1000 1500 per unit certified)

The APU Quality Leader position coordinate Quality members inside the APU, coordinate process and product audit, train and coach the Logical Thinking. This position cannot supersede Site Quality Manager authority. Initiate the QRQC in QIM database participate to the containment and validate the robustness of the containment Support APU Managers / Site Manager in the analysis of issues assigned in the QRQC activities Update the APU quality tracking charts : Customer Returns Cost of Non Quality Perform audits on the line to detect non-respect of the Standard and identify with the APU the actions to be completed to therefore comply with the Standard Participate in the eradication of Customer issues and Non Quality issues Along the APU QRQC meeting ensure that rules are respected and Stop at first disagree and Stop at first no are applied Perform the revision of the control plan after an issue Verify 4M matrix respect with regards product or process changes and ensure customer awareness and approval of changes in accordance with the 4M matrix Update the quality documents following a process related change Verify the continuous conformance of the process to generate product to specification in accordance with the control plans (machine capability yearly product audit ) Has authority to stop a manufacturing / assembly line in any situation where Standards are not respected or a safety or quality risk for the operator or for the customer has been detected or following a LLC Stability audit demonstrating lower than 100% Represent Customer within Valeo on Quality matters (communication/Escalation) Job: Quality - Operations Operational Organization: Site Quality Schedule: Full time Employee Status: Regular Job Type: Permanent contract Job Posting Date: 2025-07-17 Join Us ! Being part of our team, you will join: - one of the largest global innovative companies, with more than 20,000 engineers working in Research & Development - a multi-cultural environment that values diversity and international collaboration - more than 100,000 colleagues in 31 countries... which make a lot of opportunity for career growth - a business highly committed to limiting the environmental impact if its activities and ranked by Corporate Knights as the number one company in the automotive sector in terms of sustainable development More information on Valeo: https://www.valeo.com

You will be responsible for understanding part drawings and inspection standards in a manufacturing company. Your role will involve coordinating shift Quality operations according to standard operating procedures and reporting to the Quality In charge. You will be required to measure products using tools such as Vernier Caliper, Gauges, Micrometer, and Height Gauge. Knowledge of VMS is an added advantage. Your duties will include inspecting parts with reference to the inspection standard, ensuring that shift-produced parts meet specifications, and escalating any abnormalities. You will also be responsible for preparing inspection reports based on inspection results. Maintaining a safe and healthy work environment by adhering to standards and procedures, as well as complying with legal regulations, will be crucial. Your contribution to the accomplishment of quality and organizational goals by fulfilling related tasks as required is essential. The ideal candidate for this position should hold an ITI or Diploma qualification with a minimum of 1-3 years of experience as a Quality Engineer in a manufacturing company. Experience in Injection molding and handling plastics is preferred and considered an additional advantage. This is a full-time position based in Tumkur with a salary ranging from 20,000 to 25,000/- per month. The benefits include provided food, and the work schedule involves rotational shifts. The work location will be in person.,

Provide technical and scientific leadership to support upstream processes for early-stage development to ensure seamless handover to commercialization and life-cycle management of Sun s Branded Portfolio products manufactured internally and by a third-party suppliers/vendors. Contribute quality input into CMC strategy and execution to ensure robust supply and advance the company s portfolio. Represent and perform quality oversight duties in process development, characterization, scale-up, validation, tech transfer. Representation at Project Team and CMC meetings to plan for Clinical trial materials and collaborate with teams for handover to Commercial QA and manufacturing Provide scientific leadership in functional area to support process, product investigations (including excursions) and troubleshooting. Provide technical expertise and leadership to identify opportunities, oversee experimental planning and design, and analyze / trend, interpret, and document development results and review manufacturing data. Authoring and review of CMC documentation for regulatory filings. Responsible to support health agency and QP queries and inspections. Be an active engaged team member of the Development Quality team, support Management Review, represent Development QA in functional area meetings, as appropriate. Other tasks and audits to be performed as assigned by Management. Qualifications / Educational Requirements MS or PhD in chemical/biochemical engineering, biochemistry, or related area with 10+ years of relevant experience. Skills / Experience Requirements Proven record of quality - technical manufacturing experience; ability to influence and drive technical quality rigor; capability for strategic analysis and issue resolution Proven ability to work in a fast-paced environment with demonstrated capacity to manage multiple projects, tasks, timelines and demands Experience risk-based approaches in decision-making related to development, characterization, and manufacturing of drug products, devices and/or biologics. Demonstrate a collaborative teamwork and strong interpersonal skills Demonstrated ability to communicate appropriately and effectively Demonstrated organizational and project management skills working in a matrix environment. Experience performing audits in global regions is a preferred. VISA to travel to US and/or EU countries is a plus.

Operations Executive ReCircle recently entered the textile waste management supply chain. One of the most effective methods for reusing textile waste is transforming it into rags intended for industrial use. This approach not only significantly contributes to sustainability but also ensures that valuable materials do not end up in landfills. We are now looking for a Operations Executive to oversee the production and quality of textile rags, manage inventory. This role is ideal for someone with a mix of operational and accounting skills who can ensure the seamless execution of the manufacturing process. Key Responsibilities Operations & Quality Control Inspect and ensure the quality of rags made from textile waste. Monitor the production process to ensure efficiency and minimal waste. Coordinate with workers to maintain standard operating procedures. Ensure processes are set and followed by the manufacturing team. Inventory & Accounting Management Maintain accurate inventory records of raw materials and finished rags. Manage stock movements and ensure optimal stock levels. Update and maintain records, including financial transactions, sales, and expenses on Excel and company software. Develop and maintain relationships with customers, vendors, and partners. Requirements Experience: 1-3 years in operations, or inventory management (preferably in textiles, waste management, or manufacturing). Skills: Proficiency in Excel for inventory and accounts management. Good communication & negotiation skills. Is comfortable speaking Marathi, Hindi, and English Ability to work independently and manage multiple tasks. Other: Willingness to work on-ground and interact with vendors, workers, and clients independently Location: Dombivali, Thane

Head quality operation in the laboratory Maintenance of measuring and testing equipment Finalizing quality reports Liaise with customers and statutory bodies Experience in Coal and Minerals. Required Candidate profile 4 days internal auditor training: ISO 17025, EIC 17025 (For Quality Manager).

The Senior Manager Quality Operations role based in Hyderabad within the Customer Service- Trust & Safety domain is seeking immediate joiners who will be responsible for leading a multi-faceted independent quality evaluation process. You will oversee the measurement of quality across various sources and provide valuable insights from the operation. Your role will involve effectively managing and mentoring a team handling diverse workflows, Quality channels, and global stakeholders. It is crucial to drive accountability within the teams to achieve quality performance goals and ensure program standards are consistently met on a week-over-week basis. As a Senior Manager Quality Operations, you will assess and prioritize the top-quality issues impacting the teams across all decision-making channels. Collaboration with internal and external stakeholders is key to building scalable quality systems that enable resource-efficient monitoring of decision accuracy and faster identification of overall user experience issues. Your proactive approach will focus on driving outcomes and insights to continuously enhance and deliver an exceptional customer experience throughout the program. Additionally, you will be responsible for aggregating audit findings, analyzing process gaps, and identifying innovative solutions to solve problems upstream. This will contribute to improving customer experience, driving higher efficiency, and optimizing program operations through process management and key strategic initiatives. Your role will involve forecasting and capacity planning to meet business requirements and ensure continuity. You are expected to proactively communicate existing bottlenecks and challenges, quantify their impact on operations, and facilitate appropriate prioritization. The ideal candidate for this position should possess a minimum of 15 years of diverse experience in a scalable quality operations environment, with a track record of managing both internal and external stakeholders to drive results. Strong critical and analytical thinking, along with an entrepreneurial and proactive mindset, are essential. Experience with customer outcome and insight focus, excellent collaboration skills across functions and regions, and the ability to adapt to a fast-paced international work environment are crucial for success in this role. Exceptional communication and presentation skills are required to articulate performance trends and associated actions effectively. The ability to prioritize tasks, manage time efficiently, and perform well under high-pressure situations is vital. Fluency in English is a must, and any quality certification (e.g., Lean Six Sigma, TQM) or project management certification (PMP, Prince2) would be advantageous. In summary, as the Senior Manager Quality Operations, you will play a key role in driving quality excellence, operational efficiency, and outstanding customer experience by leading a team, collaborating with stakeholders, and implementing innovative solutions to enhance program performance.,

Role Purpose The incumbent is responsible for ensuring adherence to quality standards of both the client and GRIL, by designing the right mix, quality testing of material and calibration of equipment while collaborating with the plants & equipment team and the operations team to ensure consistency in quality. Key Responsibilities Quality Operations Ensure implementation of apex quality procedures and vehicle inspection standards. Create the design mix of materials on time while ensuring quality standards. Ensure the mix composition is maintained throughout the production through regular checks and balances. Quality compliance Adherence to established process for review of rejections with the aim to realize cost benefits. Ensure adoption & adherence to the quality guidelines. Calibration of plant equipment to adhere to set quality standards. MIS and Reporting Create the MPR and other reporting documentation for all the quality related issues and share the same with the relevant stakeholders. Indicative Experience and Exposure Graduate in (B.E./ B.Tech) Civil Engineering, preferably Post Graduation in Management/ Construction/ Transportation/ Highway Engineering/ Structural Engineering or equivalent specialized stream of Civil engineering. Min 2 yrs. of working in the area of Quality on projects with a scope of ranging around 1-5 km.

The Field Quality Manager is responsible for end-to-end monitoring of seed production fields for ensuring stringent genetic purity standards across vegetable seeds, field crops, and parent seeds. This includes close oversight during crop growth, harvest, and post-harvest stages, with strong focus on real-time deviation flagging, digital record keeping, and progress tracking via SAP and mobile applications. The role ensures implementation of quality protocols and early correction of non-compliance to uphold seed quality. Pre-Sowing Sowing Stage Hybrid Parent Seed Monitoring Harvest Post-Harvest Stage Record Keeping Quality Reporting: Key Competencies Skills Qualifications Experience 815 years experience in seed production or field quality operations. Demonstrated ability to manage large seed production areas with digital tools. Prior experience in SAP environment and mobile-based quality recording preferred. Qualification : M.Sc. Agriculture (Seed Science, Genetics Breeding, Agronomy, or related field)

SAESI MRO Tooling Engineer M/F - India, Aviation Sez Limited, Shamshabad Mandal, Ranga Reddy Dist, 500108 Hyderabad - 160316 | Safran SAESI MRO Tooling Engineer M/F 07.08.2025 Safran Aircraft Engines Services Spoken language(s) : Job Description Responsibilities: Reception of tooling and management of tool acceptance sheet Checking conformance and good condition of the tools Scanning and integration of documentation in dedicated software Checking consistency in data as per the existing documents Providing approval of the reception to Purchase team Creating work orders to ensure that tools used by operations are in good condition, properly calibrated and managed within the production line Managing the tooling fleet in dedicated software keep up to date the configuration of purchased tools: analyze evolutions, update tools. Managing tool shop layout Designing and validating tooling design Proposing design change for improved efficiency Job Requirements o Work in an orderly and precise way, be reliable in his/her proposals. o Ability to listen, animate, coordinate, synthesize and formalize o Have team spirit: strong relationship with the methods and industrialization, Quality, Operations and HSE teams. o Have a creative mind Company Information Safran is an international high-technology group, operating in the aviation (propulsion, equipment and interiors), defense and space markets. Its core purpose is to contribute to a safer, more sustainable world, where air transport is more environmentally friendly, comfortable and accessible. Safran has a global presence, with 100,000 employees and sales of 27.3 billion euros in 2024, and holds, alone or in partnership, world or regional leadership positions in its core markets. Safran is in the 2nd place in the aerospace and defense industry in TIME magazines "Worlds best companies 2024" ranking. Safran Aircraft Engines designs, produces and sells, alone or in partnership, commercial and military aircraft engines offering world-class performance, reliability and environmental compliance. Through CFM International*, Safran Aircraft Engines is the worlds leading supplier of engines for single-aisle mainline commercial jets. * CFM International is a 50/50 joint venture between Safran Aircraft Engines and GE Aerospace Number of countries where Safran is located

1 Responsible for lifecycle management of DSRM procedural documents in EDMS and non-procedural documents within due date which includes document creation, document revision, making document obsolete, making document effective, releasing document, sharepoint update and communication to relevant stakeholders 2 Responsible as SOP coordinator to perform roles as Author in edit step and QA authorisation in Release approval step 3 Responsible to perform role of Training Coordinator in Training step within EDMS as required 4 Oversight and management of compliance of DSRM training requirements and activities in LMS 4 Support and oversight of subsidiary Global PV training status as applicable 5 Oversight and management of Annual Basic PV compliance for India 6 Oversight on teams task completion, annexures, sharepoint updates and people management. 7 Creation of status presentations and other adhoc presentations as required People Management Competencies Strategic Agility Innovation & Creativity Process Excellence Customer Centricity Collaboration Stakeholder Management Developing Talent Result Orientation Education- Life Science Post Graduate, MPharm, BPharm, Work Experience Experience in Pharmacovigilance operations, Quality Management System, Training, Use of Systems for SOPs and Training Management

Elevate your career as a Reconciliation Senior Specialist II, where youll be at the forefront of delivering top-quality operations and driving process excellence. In this pivotal role, youll support your team and leader by meticulously documenting procedures and identifying opportunities for enhanced controls. Job Summary As a Reconciliation Senior Specialist II within the Operations Team, you will support the team and team leader in delivering top-quality operations, document procedures, and identify additional control requirements. Job Responsibilities Responsible for ensuring good and effective reconciliation by gaining a thorough understanding of the product. Ensure adherence to operational procedures to complete tasks accurately and promptly. Support the team and team leader in their mission to deliver top-quality operations. Identify requirements for additional controls. Complete daily checklists and reporting, actively collaborating with the team to resolve exceptions. Prepare case notes, discuss learnings with the team, and seek opportunities to improve process efficiency. Perform effectively in a fast-paced environment, handling multiple tasks through effective prioritization. Work effectively with the team leader and serve as a backup in their absence. Ensure that the latest process updates and changes are communicated to the team and understood by all team members. Escalate any matters of concern to the team leader promptly and ensure issues are resolved. Required qualifications, skills and capabilities Ability to work a flexible shift as required. Ability to perform in a fast paced environment and handle multiple tasks through effective prioritization. Strong analytical and problem solving skills. Excellent written and oral communication skills. Strong team player and has the capacity to build good working relationships with cross functional/geographical teams. Result oriented, accepting responsibilities and challenges that take them outside their comfort zone. This role requires meticulous attention to detail. Proficiency in Microsoft Office Suite (Word, Excel, Access, PowerPoint) required. Elevate your career as a Reconciliation Senior Specialist II, where youll be at the forefront of delivering top-quality operations and driving process excellence. In this pivotal role, youll support your team and leader by meticulously documenting procedures and identifying opportunities for enhanced controls. Job Summary As a Reconciliation Senior Specialist II within the Operations Team, you will support the team and team leader in delivering top-quality operations, document procedures, and identify additional control requirements. Job Responsibilities Responsible for ensuring good and effective reconciliation by gaining a thorough understanding of the product. Ensure adherence to operational procedures to complete tasks accurately and promptly. Support the team and team leader in their mission to deliver top-quality operations. Identify requirements for additional controls. Complete daily checklists and reporting, actively collaborating with the team to resolve exceptions. Prepare case notes, discuss learnings with the team, and seek opportunities to improve process efficiency. Perform effectively in a fast-paced environment, handling multiple tasks through effective prioritization. Work effectively with the team leader and serve as a backup in their absence. Ensure that the latest process updates and changes are communicated to the team and understood by all team members. Escalate any matters of concern to the team leader promptly and ensure issues are resolved. Required qualifications, skills and capabilities Ability to work a flexible shift as required. Ability to perform in a fast paced environment and handle multiple tasks through effective prioritization. Strong analytical and problem solving skills. Excellent written and oral communication skills. Strong team player and has the capacity to build good working relationships with cross functional/geographical teams. Result oriented, accepting responsibilities and challenges that take them outside their comfort zone. This role requires meticulous attention to detail. Proficiency in Microsoft Office Suite (Word, Excel, Access, PowerPoint) required.

What You'll Do We are looking for a strategic Senior Manager Quality Operations to lead our quality assurance programs across customer-facing operations. You will be pivotal in driving Continuous Improvement (CI) , optimizing audit programs, and enhancing through data, insights and collaboration. You lead with insight, think in systems, and act on datatransforming complexity into clarity and action who excels at optimizing complex processes, building teams, and driving continuous improvement through evidence-based decision-making. You will report to the Director of Quality and Data What Your Responsibilities Will Be Quality Strategy: Design, manage quality frameworks across multiple departments (e.g., Notice Management, Case Management, Transactions). Lead the development of scorecards, sampling methodologies, and audit processes to improve process consistency and customer satisfaction. Continuous Improvement (CI): Champion CI culture by identifying causes, process inefficiencies, and improvement opportunities. Facilitate Lean/Six Sigma-inspired projects to lead measurable gains in quality and operational efficiency. Build capability across teams by promoting CI methodologies into daily operations. People Leadership: Mentor a team of data-centric quality professionals, encouraging a culture of analytical rigor, learning, and new ideas through coaching, and strategic recognition. Build team accountability and engagement through clear goals, performance metrics, and regular feedback loops. Stakeholder Management & Collaboration: Collaborate with Ops, Compliance, Automation, Data, and Support teams to align QA goals and guide shared outcomes. Provide guidance to leadership on process improvements, audit insights, and customer pain point resolution. Insights & Governance: Deliver relevant insights from quality audits and customer feedback to inform process, product, and training strategies. Ensure adherence to compliance standards and risk mitigation through proactive QA practices. What You'll Need to be Successful 10+ years of experience in Quality, Operations, or Process Excellence roles Proven track record in driving data-informed quality improvements, with practical application of methodologies like Lean and Six Sigma to enhance operational processes. People management experience, including team building and cross-functional leadership Proficiency with QA tools and platforms (Salesforce, Freshdesk) and data tools (Excel, Tableau, Power BI) Required skills: Continuous Improvement & Problem Solving Leadership & Team Development Develop data-driven strategies that align quality projects with broader goals. Operational & Risk Awareness Partner Influence & Collaboration Data-Driven Decision-making