90 Quality Operations Jobs

Liaise with the reagent contract manufacturer and represent Beckman Coulter Quality in the interaction with the contract manufacturer and is responsible for the generation, analysis and reporting of quality metrics to relevant personnel and to ensure on-going improvement programs are put in place. Lead cross functional teams providing Quality guidance and guide in the determination of appropriate NC root cause analysis and implementation of effective corrective actions. Responsible for the Rework process, ensuring relevant documentation is prepared, reviewed and approved as per company procedures as well as completing Acceptable Quality Level (AQL) inspections prior to product disposition. Execute the Stop Ship process for finished product released to the market, in the Oracle system, ensuring process is compliant to relevant company procedures and perform CAPA (corrective and preventive action) activities and document in the CAPA system if required. Review & Approve document Change Controls (CCFs) and Equipment Change Controls (ECCs) ensuring Good Manufacturing Practices are maintained and comply with company procedures. Author relevant procedures, Review/Approve documentation (e.g. protocols, reports) ensuring compliance to applicable procedures and provide Quality expertise during the product life cycle. Review & Approve Certificate of Analysis(COA) for the finished goods.

As a Principal Quality Operations Specialist at Lutech Resources, you will be responsible for interpreting internal and external business challenges in the operations discipline. Your role demands specialized depth and breadth of expertise in operations to ensure the highest quality standards are maintained. Key Responsibilities: - Visit and perform inspections at suppliers" premises/sites to determine product conformity to Purchase Orders (PO), drawings, data sheets, and technical specifications through inspection and tests per Quality/Inspection & Test Plans. - Liaise with Manager Assurance, Source Inspection Coordinator (SIC), Package Manager/Engineer, Assurance Specialist, Discipline Engineer, Expeditor, Certifying Authority, Customer representatives, and Suppliers. - Lead inspection activities on critical packages to ensure product conformance based on approved documents and latest deliverables. - Appraise product quality in line with Purchase Orders/Purchase Requisitions, Technical Specifications, drawings, and Quality Plans. - Ensure no open Non-Conformance Reports (NCR) on the equipment/package before release. - Conduct In-process, Final Inspection, and Witness Factory Acceptance Test per approved procedures and project specifications. - Perform quality audits and surveillance to assess supplier compliance with approved procedures and verify the effectiveness of the Supplier Quality System. - Review inspection assignment package, identify change and progress issues, and liaise with Package Manager and Manager Assurance. - Attend various meetings as required, issue Meeting Minutes (MOM), and prepare necessary reports. - Sign off on Inspection and Test plans, prepare Supplier Inspection Reports (SIR), and document all inspection results including non-conformances for corrective action. - Identify outstanding work, record in a punch list format, and attach to the Supplier inspection report/Inspection release. - Monitor project document requirements and progress to the final data dossier following the approved Manufacturers Data Record or Quality dossier index. - Stamp and sign all reviewed documents/test reports/certificates and actively monitor inspection activities to eliminate potential quality issues. Qualifications Required: - Bachelor's Degree/Diploma in Mechanical Engineering or Equivalent. - 15+ years of experience in source inspection of critical packages such as Static equipment's, Rotary Equipment's, Structural and Piping bulks, Skid Mounted Equipment's, Line pipe, etc. - NDT Level-II certification in PT, MT, UT, RT. - Welding Inspector certification in AWS/CSWIP. In addition to the job responsibilities and qualifications, Lutech Resources is a global company with over 25 years of experience providing tailored recruitment and integrated resource management to leading Engineering, Energy, and Manufacturing sector companies worldwide. We focus on building long-term relationships with clients and candidates based on industry understanding and a commitment to excellence, striving for positive outcomes for all stakeholders involved.,

So what does a Quality Manager really do? Think of yourself as a champion for operational excellence. You will closely monitor program metrics, provide insights and analysis, offer recommendations, and help manage the implementation of service and process improvement programs and efforts. Your contribution will help ensure program metrics and service level requirements for quality are met consistently. You will also take the lead in conducting quality audits, report on findings, and propose new systems and policies for continuous improvement. Consider yourself a consultant to stakeholders, a mentor and guide to Teams, and an important asset to our passionate pursuit for quality. Imagine yourself going to work with one thing on your mind: you are responsible for your programs achievement of performance objectives, ensuring consistency and quality in all customer interactions. As you tackle new tasks for the day, you know that it will lead to one thing: raising the bar for our quality operations to produce ridiculously impressive outcomes. As a Quality Manager, you will leverage on your analytical skills to create a metric-driven determination of our successes. You will identify opportunities for improvement and help develop impactful and measurable action plans to address these. You must be highly motivated by the opportunity to effect change and bring these plans to fruition. So do you have what it takes to become a Quality Manager? Requirements: At least three (3) years of experience in quality management in a BPO environment Excellent communication and presentation skills Knowledgeable in performance data management and analysis We need someone with strategic capability, expert competency in problem solving, and a strong drive for results and excellence. Someone who can cultivate effective and productive business relationships to resolve outstanding quality issues in collaboration with other Quality Assurance leaders.

So what does a Quality Manager really do? Think of yourself as a champion for operational excellence. You will closely monitor program metrics, provide insights and analysis, offer recommendations, and help manage the implementation of service and process improvement programs and efforts. Your contribution will help ensure program metrics and service level requirements for quality are met consistently. You will also take the lead in conducting quality audits, report on findings, and propose new systems and policies for continuous improvement. Consider yourself a consultant to stakeholders, a mentor and guide to Teams, and an important asset to our passionate pursuit for quality . Imagine yourself going to work with one thing on your mind: you are responsible for your programs achievement of performance objectives, ensuring consistency and quality in all customer interactions. As you tackle new tasks for the day, you know that it will lead to one thing: raising the bar for our quality operations to produce ridiculously impressive outcomes. As a Quality Manager , you will leverage on your analytical skills to create a metric-driven determination of our successes. You will identify opportunities for improvement and help develop impactful and measurable action plans to address these. You must be highly motivated by the opportunity to effect change and bring these plans to fruition. So do you have what it takes to become a Quality Manager ? Requirements: At least three (3) years of experience in qualitymanagement in a BPO environment Excellent communication and presentation skills Knowledgeable in performance data management and analysis We need someone with strategic capability, expert competency in problem solving, and a strong drive for results and excellence. Someone who can cultivate effective and productive business relationships to resolve outstanding quality issues in collaboration with other Quality Assurance leaders.

Role & responsibilities Key Duties & Responsibilities Daily Operations: Coordinate and manage daily activities across all departments (front desk, housekeeping, maintenance, F&B) to ensure seamless operation. Guest Experience: Ensure high standards of guest service, address complaints, and actively work to improve guest satisfaction scores. Staff Management: Recruit, train, schedule, and supervise hotel staff, fostering a positive and productive work environment. Financial Oversight: Manage departmental budgets, control expenses, monitor financial performance, and report on key metrics to senior management. Quality Control: Implement and enforce operational policies, procedures, and health & safety standards to maintain facility quality and guest safety. Inventory & Supplies: Monitor and manage inventory levels, ensuring all necessary supplies and equipment are ordered and maintained. Collaboration: Work closely with department heads, sales, and marketing teams to align strategies and achieve business goals. Problem Solving: Resolve issues promptly, both operational and customer-related, often requiring quick and effective decision-making. Essential Skills & Qualifications Leadership & Management: Ability to effectively lead, motivate, and develop a team. Communication: Excellent verbal and written communication skills for clear interactions with staff, guests, and management. Customer Service: A strong commitment to providing excellent service and exceeding guest expectations. Financial Acumen: Skills in budget management, cost control, and financial analysis. Problem-Solving: Strong analytical and problem-solving skills to handle unexpected situations and challenges. Industry Knowledge: Understanding of the hospitality industry, including current trends and best practices. Education: Often requires a degree in hospitality management, business administration, or a related field. Experience: Several years of experience in a supervisory or managerial role within the hospitality industry is crucial.

Assist in developing fundraising strategies and execution plans in alignment with organizational goals, under the guidance of the vertical head, and make a time-bound roadmap to implement the same. Work closely with other departments, such as communications, finance, program operations quality, to ensure fundraising activities align with overall organizational objectives. Cultivate relationships with existing donors, prepare materials for donor meetings, and assist in donor stewardship activities to maintain positive relationships. Write and prepare compelling proposals, grant applications, and fundraising materials to secure funding. Ensure donor reports are prepared with comprehensive and accurate data and timely submission of the same. Write, build, and submit concept notes, budgets, and proposals in close collaboration with the vertical head. Make grant estimates and align funding opportunities accordingly. Manage the team and mentor, guide, and drive them to the achievement of their goals, fostering a culture of learning and growth. Stay updated on industry trends, new technologies, and innovative fundraising methods. Monitor completion of project deliverables in collaboration with program and implementation teams. Provide partners with timely and accurate information about project progress. Proactively communicate challenges and recommend solutions

Performing day to day activities of processing market complaints assigned as per the relevant SOPs, business matrix and SLA timelines. Assist in data collection and reporting of KPIs Assist in continuous improvement initiatives. Manage ad-hoc projects assigned in area of work. Proactively report all deviations through timely escalations Implement continuous process improvement projects to enhance quality & productivity. Ensure that the service dashboard, order management framework & time sheet are always kept updated. Ensure Training on relevant procedures before taking up any GxP activities. Report deliverable status and continuously acquire process knowledge. Role Requirements : 5-8 years of relevant experience in Quality Operations. Thorough understanding of Quality Management Systems. Able to review the market complaints investigation reports. Basic understanding of product manufacturing, Pharma products and lifecycle events. Basic understanding of Track wise. Basic understanding of performance KPIs. Basic understanding of MS Excel. Awareness of GXP Communication Skill - Fluent in verbal and written English; knowledge of other languages is an added advantage. Desirable Requirements: Graduate / Post Graduate in Pharmacy.

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) In case of APU Quality Leader position, he will report to this position and will not supersede APU Quality Leader and Site Quality Manager authority. In charge of PD , CA and closure management for Internal Suppliers incidents.

About Us: Mahindra Logistics Limited is a leading integrated logistics & mobility solutions provider with over a decade of experience. We have a strong presence across the country. We offer Supply Chain solutions to diverse industry verticals such as Automotive, Engineering, Consumer Goods, Pharmaceuticals, Telecom, Commodities, and E-commerce and also offer integrated employee transportation solutions to enterprise across IT, ITeS, manufacturing, Banking, Financial Services and Insurance, and Consulting Businesses. What you will learn and contribute to (Key Responsibilities): Quality control. Inventory Management. Handling Dispatch planning. Handling transport Operation. Handling Vendor as well as clients queries and asculation. Critical Competencies : Good in verbal and mail communication. Should be well versed with Quality Operation. Should be well known with SAP MM Module. Good problem solving and analytical skills. Enthusiastic learner who is ready to take up new challenges. Should be team player. Experience: 3/6 Years. Qualifications: Bachelor in Engineering.

We are looking for a talented and experienced Technical Program Manager who is excited to lead large cross-organizational projects and initiatives. In this role, you will work hands-on with engineering, leadership and Product Management teams to deliver results while fostering input and participation from all levels of the organization. You work on features that directly impact millions of Amazon customers. You will have the opportunity to provide direction to our businesses and guide the design of our systems based on realistic time lines and resource constraints. Success in this role requires you to think strategically. You will perform deep dive analytics on existing processes, identify where process and system improvements are needed, define the desired state solutions, and work through dependencies to establish key project milestones and business requirements. Join us and realize your potential for growth and development. The role requires you to be able to manage the overall software development life-cycle which includes the following responsibilities: Create, prioritize, communicate, manage, and execute roadmaps, project plans, and commitments. Report on status of development, quality, operations, and system performance to management. Work closely with engineers to architect and develop the best technical design and approach. Foster culture of continuous engineering improvement through feedback, and metrics. Partner with a diverse stakeholders to understand requirements, priorities, and processes. Propose and implement new projects or recommend system improvements. Have the obsession to drive a better customer experience through everything that we do here at Amazon. Bring innovative ideas to the table every day, in order to find better ways of accomplishing our customer objectives. Set clear, measurable quality goals for an organization in a data-driven way. 7+ years of working directly with engineering teams experience 5+ years of technical product or program management experience 3+ years of software development experience 5+ years of technical program management working directly with software engineering teams experience Experience managing programs across cross functional teams, building processes and coordinating release schedules 5+ years of project management disciplines including scope, schedule, budget, quality, along with risk and critical path management experience Experience managing projects across cross functional teams, building sustainable processes and coordinating release schedules Experience defining KPIs/SLAs used to drive multi-million dollar businesses and reporting to senior leadership

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).

A successful candidate will be a hands-on manager with an established background in developing high volume and highly available services, strong technical ability, great communication skills, and a motivation to achieve results in a dynamic, fast paced environment. Build a best-in-class engineering team that delivers excellent results through rapid iterations Design and develop state-of-the-art approaches to solving complex and ambiguous problems Cultivate engineering and operational excellence through metrics and continuous learning Develop long term strategy for your programs and translate it into roadmap and action plan Report on status of development, quality, operations, and system performance to management Mentor and grow superstar SDEs to take on increasingly higher responsibilities

The Opportunity: Officer - Quality Control is responsible to perform Quality Control activities at AQAL. What we are looking for :- Responsible for Timely analysis of under test samples giving timely results Coordination with tollar for quality related issues and clarification Sampling and analysis for RM/Intermediate/Finished Goods. Ensure compliance of ATR. Assisting team in ISO implementation Knowledge of calibration, standard preparation, standardization and relevant documentation. Handling knowledge of HPLC,GC and wet analysis. Education: B. Sc. M. Sc. (Chemistry) Experience: 2-5 years of experience in Quality including cGMP, ISO and regulatory Audits Preferred Skills/Qualifications: Knowledge of Quality Control in Fine Chemicals and pharmaceutical company. Experience of cGMP Skills/Competencies: Willingness to learn Team Player Good communication skills How you will thrive and create an impact :- Give timely reports to SAP for result recording. Fill and update all documents. Zero accidents in the Quality operations. Achieving batch wise timelines, quantity and quality. Will train & supervise the working of all operators working in his dept. Will monitor the waste generated during operation. Will be member of the Emergency response team and will guide & train other team members in case of Emergency. Maintain ISO 9001:2015, SAP, and other Quality system into department. Will maintain the analytical records log sheets as per GMP & ISO guidelines.

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.

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company's patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization. Brief Team/department Description: Technical Operations is responsible for management and oversight of technical process strategy, CMO and CDMO management, and execution of product deliverables in alignment with Azurity policies, Azurity clients and in accordance with company objectives. The position leads staff and / or contractors and collaborates cross-functionally to achieve project milestones in support of process scale-ups and process validation, technical transfers, implementation of lifecycle post approval changes, and investigation / closure of deviations / OOS for commercial products. Principle Responsibilities: - Manage the planning and execution of manufacturing along with associated qualification and validation activities as they relate to both development and commercial products. - In cooperation with contract facilities, manage the review, approval, and execution of controlled documentation concerning late-stage development, qualification, validation, and commercial manufacturing activities as needed. - Direct tasks associated with late stage product / process development (as applicable), product transfers, equipment qualifications, and validation activities to ensure alignment with company policies and objectives. - Support and / or lead product launch and commercialization efforts. - Ensure that appropriate policies, SOPs and documentation are in place to support validation practices according to regulatory requirements and applicable industry guidance documents. - Support Management Review and Compliance related activities as needed. - Assist in preparing metrics and compiling summaries to effectively communicate status and recommendations to Senior Management. - Support Due Diligence activities to support company objectives including product development, technical transfer, commercial manufacturing, and/or commercial launch. - Collaborate closely with cross-functional team members from functions including Supply Chain, Product Development, Quality Assurance, and Regulatory Affairs. Qualifications And Education Requirements: - Bachelor's degree in Life Sciences (Master's Degree preferred), or related field. - Minimum 15 years of experience in biopharmaceutical/pharmaceutical GMP environment or related industry. - Expertise in cGMPs, ICH and Validation related requirements and guidances - In-depth experience in performing technical transfer of multiple dosage forms (solid oral, liquid oral, injectables, etc.) - Experienced in multiple validation disciplines including manufacturing process validation of multiple dosage forms, cleaning validation, packaging validation, analytical methods validation, terminal sterilization validation, hold time studies, shipping studies, equipment / utilities qualification, and facilities validation - Ability to work in a strategic, tactical, and hands-on level. - Candidate must be proficient in Microsoft Word, Excel, and Powerpoint. - Experienced in participating in regulatory agency inspections. - By applying for this role, you confirm that you are mentally and physically capable of fulfilling the job responsibilities detailed in the job description without any restrictions. If you have any concerns or even the slightest disability that may affect your ability to perform the job, please inform HR in advance.

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 Process Analyst position in Bangalore requires a minimum of 2 years of experience, preferably in the ITES or BPM industry. As a Process Analyst, you will report to the IND Group Manager, Global Business Process Management and play a crucial role in supporting process improvement and documentation initiatives. Your responsibilities will include assisting in gathering process information and requirements through interviews and workshops with business stakeholders, documenting and visualizing business processes using BPMN 2.0 notation, and preparing and maintaining process maps, SOPs, and related documentation. Additionally, you will coordinate process review sessions, collaborate with senior analysts and process improvement experts, track process performance metrics, and ensure up-to-date process documentation. The ideal candidate for this role will have at least 2 years of experience in Quality, Operations, Process Documentation, or similar areas within the ITES or BPM industry. You should be familiar with business process documentation and mapping, have some experience using tools like Microsoft Visio or other process mapping/BPM software, and possess a basic understanding of BPMN 2.0 notation. A Lean Six Sigma White Belt certification is required, and a Yellow Belt certification or similar process improvement training is a plus. Strong organizational, planning, and communication skills are essential, along with the ability to work well within teams. An eagerness to learn about process performance metrics and data-driven improvement is also important. The Process Analyst role offers the opportunity to develop expertise in BPMN process mapping and Lean Six Sigma methodologies. By joining this team, you will contribute to process design and transition exercises, identify improvement opportunities through basic analysis, and maintain version control of process documentation. If you are a motivated and detail-oriented individual with a passion for process improvement, this position may be the perfect fit for you.,

As an AIN Specialist QA at Amgen, you play a critical role in supporting product disposition tasks across the Quality Operations Network. Leveraging your industry, technical, and quality systems knowledge, you ensure efficient management of product expiry processes, product complaints, disposition manager training, and fulfillment of related data requests. Your responsibilities include executing GMP processes for shelf-life extension, supporting partner requests for data related to partnered product batches, generating Certificate of Analysis records, providing training to new disposition managers, and conducting full batch record reviews for product complaints. You will primarily work during regular hours to assist in delivering Amgen's mission of serving patients and may lead a team providing coverage across multiple time zones. Flexibility to work outside regular hours and from the office in Hyderabad, India, is required. Moreover, you will lead remote support to Amgen sites globally. Key responsibilities also involve extending expiration dates for products, updating batch information in the SAP inventory system, evaluating expiry-SAF forms, supporting partner requests for data recovery, generating COAs, providing training to new managers, and conducting batch record reviews for product complaints. Preferred qualifications for this role include experience in project management, proficiency in technical writing and data visualization tools, excellent communication skills, ability to lead cross-functional teams, and experience in manufacturing environments. Core competencies required include working in a regulated environment with knowledge of GMP and GDP requirements, familiarity with Quality Systems such as ERP/SAP, RIM, CDOCS, QMTS, DQMS, and LIMS, staff training experience, and technical document drafting. The basic qualifications for this position include a Master's degree with 8-12 years of experience in Pharma and Biotech commercial or clinical manufacturing Quality. If you are passionate about making a lasting impact on patients" lives through innovative medicines and are eager to contribute to a collaborative and science-based culture, join us at Amgen and transform your career while transforming the lives of patients.,

As a Process Analyst at our Bangalore location with 2+ years of experience, preferably in the ITES or BPM industry, you will be reporting to the IND Group Manager, Global Business Process Management. Your primary responsibility will be to support process improvement and documentation initiatives by collaborating with business teams and senior analysts. Your role will involve capturing, documenting, and optimizing business processes, making it ideal for individuals with a background in quality operations, process documentation, or transitions. This position offers the opportunity to develop expertise in BPMN process mapping and Lean Six Sigma methodologies. Your key responsibilities will include assisting in conducting interviews and workshops with business stakeholders to gather process information, learning to document and visualize business processes using BPMN 2.0 notation, supporting the preparation and maintenance of process maps and SOPs, coordinating process review sessions, collaborating with senior analysts during process design and transition exercises, tracking process performance metrics, and maintaining up-to-date process documentation. To excel in this role, you should have 1-2 years of experience in a supporting role within Quality, Operations, Process Documentation, or similar areas, familiarity with business process documentation and mapping, some experience using tools like Microsoft Visio or other process mapping/BPM software, basic understanding of BPMN 2.0 notation, Lean Six Sigma White Belt certification, good organizational, planning, and communication skills, eagerness to learn about process performance metrics, and data-driven improvement. Preferred qualifications include exposure to process improvement or transition projects, Yellow Belt certification or similar process improvement training, and basic awareness of process mapping notation tools, process automation, or concepts. At our organization, we are committed to sustainability and integrating it into our core business practices to minimize environmental impact and ensure a sustainable future for our clients and communities.,

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