242 Quality Compliance Jobs - Page 2

Role Overview The Senior Manager Quality Control will lead and oversee all quality assurance activities across casting, foundry, welding, and machining operations. The role demands deep technical expertise, strategic leadership, and hands-on experience in ISO standards and industrial quality systems. Familiarity with materials such as HDPE, plastics, and rubber is highly desirable. Key Responsibilities : Quality Leadership * Develop and implement robust quality control systems across manufacturing processes * Lead root cause analysis and corrective/preventive actions (CAPA) for quality issues * Ensure compliance with ISO 9001 and other relevant standards * Drive continuous improvement initiatives using tools like Lean , Six Sigma , and Kaizen Technical Oversight * Monitor and audit quality in casting, foundry, welding, and machining operations related to Wedge and Anchor , bearing plate ,couplers and other ancillary product developments * Define inspection protocols and quality benchmarks for raw materials and finished goods * Collaborate with engineering and production teams to resolve quality challenges * Supervise calibration and maintenance of testing equipment Material & Process Expertise * Evaluate and ensure quality standards for HDPE, plastics, rubber , and other polymers * Review vendor quality performance and support supplier development programs * Conduct internal and external audits and ensure documentation compliance Team & Stakeholder Management * Lead and mentor a team of quality engineers and inspectors * Interface with clients, vendors, and regulatory bodies on quality matters * Prepare and present quality reports and dashboards to senior leadership Qualifications & Skills * Bachelor's degree in Mechanical Engineering (Master's preferred) * 15 to 20 years of experience in industrial quality control, preferably in manufacturing * Strong knowledge of ISO standards , casting , welding , and machining processes * Familiarity with HDPE, plastics, rubber , and polymer-based materials * Excellent analytical, leadership, and communication skills * Proficiency in ERP systems and quality management software

The Quality Compliance Senior Manager is a global role and part of the Clinical & Research Quality (CRQ) team for the R&D Quality Organization. CRQ organization plays a critical role in ensuring that our research and development activities are conducted in an ethical and responsible manner . CRQ is responsible for ensuring that our research and development activities meet the highest standards of quality and compliance, ultimately keeping patients safe, protecting their welfare, while ensuring that all data produced has integrity. In this vital role , the Quality Compliance Senior Manager will contribute to providing leadership to ensure excellence in R&D Quality Processes is maintained through oversight and improvements when compliance issues are identified In addition, this role will serve as a mentor for Amgen staff in India who will be working to advance the Quality System, and they will act to manage day to day activities for the team. They will be an integral team member working globally with Business Process Owners to ensure compliance with regulations and other business requirements. This role will be part of supporting the digital quality management system (DQMS) as a Subject Matter Expert ( SME ) to support the core processes managed in Quality. Additionally, the Quality Compliance Senior Manager will provide proactive end to end quality support for the management of Quality Incidents/Quality Events , working closely with Quality Leads in approving investigations , including root cause analysis (RCA) and C orrective & Preventive Action (C APA ) plans. Roles & Responsibilities: The Quality Compliance Senior Manager will work both independently and in a team environment to foster collaborative relationships with in R&D Quality. In this vital role , they will be responsible for supporting processes and operational activities related to ; overseeing deviations, preparation of audits and inspections across R&D Quality including Good Pharmacovigilance Practice ( GPvP ), Good Clinical Practice (GCP) and Good Laboratory Practice (GLP). As part of strengthening and advancing Amgen s R&D QMS, this role provides end-to-end quality support to Deviation owners, RCA owners, and CAPA owners. Manages the Amgen India R&D Quality team to ensure that the team is supported and managed on a day-to-day basis. Support s the intake, triage, and categorization of deviations, ensuring appropriate classification and documentation. Facilitate s timely and thorough deviation investigations in collaboration with functional area r epresentatives and Quality Leads. E nsure s consistent and compliant documentation of deviation records within the electronic quality management system ( D QMS). Monitor s and ensure s adherence to timelines, escalating delays and risks as needed. Support s Global Patient Safety and Global Development teams in GxP inspection management activities and GxP audits from business partners Identif ies , lead s , or contribute s to continuous improvement initiatives to enhance CAPA management practices. Collaborate s with cross-functional partners to ensure processes remain effective, efficient, and aligned with industry best practices and evolving regulations. Ensure s the integrity, traceability, and quality of deviation and CAPA records in compliance with ALCOA+ principles. Monitor s quality metrics and key performance indicators (KPIs) related to deviation and CAPA management. Analyses trends and perform root cause trending to identify systemic issues and opportunities for process improvement. Manage s , organize s and analyse s data through different systems, tools, or platforms, including Excel and Smartsheet Maintain s knowledge of current regulatory and quality practices/issues Maintain s the Global R&D CRQ and SMQ SharePoint sites Manage s the appropriate archival and retention of audit documentation. Basic Quali fi cations and Experience: Master s degree with 10-12 years of Pharma and Biotech R&D or commercial manufacturing Quality experience. Continuous Improvement/Change Management experience is preferred Additional Competencies/Skills: Exceptional attention to detail and accuracy in all deliverables. Ability to work independently and proactively in a fast-paced environment. Proficiency in Smartsheet, Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) and virtual collaboration tools (e.g., Teams, WebEx ) Good team building skills and the ability to on-board new employees and develop them over time Familiarity with project management tools and methodologies. Knowledge of GCP, GLP and/or GPvP . Experience working in a multinational environment with global teams. Excellent verbal and written communication skills. High degree of professionalism and interpersonal skills. Strong problem-solving abilities and adaptability to changing priorities. Collaborative attitude and ability to build positive relationships across diverse teams. Resilience, discretion, and the ability to thrive under pressure

Responsibilities: * Conduct quality audits & inspections * Ensure compliance with standards * Manage quality processes & systems * Analyze data for improvement opportunities * Monitor product/service quality

Role & responsibilities Above site review as part of GIT Completes above site level real time review, assessment and scoring of all aspects of Investigations including Deviations, LIRs, Complaints, CAPAs, using preapproved standard rubrics to ensure scientific rigor and discipline is applied to identify root cause for Investigations including proposal of effective CAPAs, prior to investigation closure. Submits the draft investigation report and completed rubric to the GIT on a timely basis to permit their review and feedback within the due date. Implement/reinforce Investigator and Approver Certification (IAC) rubrics / evaluation-based education and coaching for site Quality decisions on investigations and CAPA, drive continuous improvement and standardization across the organization. Ensures that investigations identify the true root cause based on Scientific rigor, Human Error causes are properly investigated, Impact and Risk level are appropriately assessed, and the corrective and preventative actions are commensurate. Ensures all comments from GIT are addressed in the final report and gets final approval from GIT before closure of investigation. Ensures that review of assigned number of investigation reports is completed as per required Works as a member of the Global Investigation Team (GIT) network to achieve a sustainable self-teaching model, to spread good investigation practices and to share learnings and best practices to Site/Function through the multiple established Forums at the sites. Acts as resource providing support and guidance to SIT, QA Approvers and Lead Investigators at the site Performs all work in support of our Corporate Values of Collaboration, Courage, Perseverance, and Passion; Demonstrate strong and visible support of our values. Performs all work in compliance with our Code of Conduct and Business Ethics, related policies and with the legal and regulatory requirements that apply to our job activities. Preferred candidate profile Education Bachelor's degree in science or a related Level 2 Certification: Investigation and CAPA Expert Knowledge, Skills and Abilities Strong knowledge and application of cGMPs/GMPs in a pharmaceutical manufacturing and in QA/QC environment Deep understanding of Investigation process and CAPA management Demonstrated ability to work independently and effectively manage multiple priorities in a fast paced and changing environment. Excellent interpersonal, communication, presentation, and facilitation Critical thinking and application of scientific reasoning Demonstrated ability to work in partnership with and build strong links to all areas of the business. Ability to provide effective feedback and coaching to others. Experience Minimum of 5 years of regulatory compliance and quality experience in the pharmaceutical or related industry with experience in quality, production or laboratory systems Minimum 3 years of practical experience in Investigations management.

You are looking for a Senior Technician in Engineering to join our team in Ahmednagar. As a Senior Technician, you will be responsible for maintaining and repairing manufacturing equipment in an API manufacturing plant. With a qualification of ITI (MMCP) and 2-7 years of experience, you will play a crucial role in ensuring the smooth operation of the manufacturing process. Your key responsibilities will include equipment maintenance and troubleshooting, where you will perform preventative and corrective maintenance to minimize downtime. Additionally, you will provide technical support for the API manufacturing process to ensure its smooth operation and adherence to established procedures. It will be essential for you to comply with quality and safety standards, including GMP (Good Manufacturing Practices), to ensure all work is performed in accordance with relevant regulations. You will also be responsible for maintaining accurate records of maintenance activities, equipment performance, and any deviations from standard procedures. In this role, you will be required to attend breakdown maintenance as and when required, contributing to the overall efficiency and effectiveness of the manufacturing plant. If you have a passion for engineering and a keen eye for detail, we invite you to apply for this exciting opportunity.,

You will be responsible for maintaining and repairing manufacturing equipment, including performing preventative and corrective maintenance, as well as troubleshooting issues to minimize downtime. Additionally, you will provide technical support for the API manufacturing process to ensure smooth operation and adherence to established procedures. It is essential to ensure that all work is performed in accordance with GMP (Good Manufacturing Practices) and other relevant quality and safety standards. You will be required to maintain accurate records of maintenance activities, equipment performance, and any deviations from standard procedures. As part of your responsibilities, you will also need to attend breakdown maintenance as and when required.,

As a Billing Engineer/Quantity Engineer at GUNNAM Infra projects in Bangalore and Hyderabad, you will be responsible for planning and billing clients, conducting rate analysis, bill estimation, costing, and verifying bills. Your role will involve preparing bill of quantities (BOQ), inspecting and verifying works measurements, processing invoices, and monitoring all site execution activities. You will be expected to perform tasks such as inventory management, reconciliation, quantity surveying activities, and ensuring compliance with quality procedures and systems on site. Your responsibilities will also include verifying and approving bills of contractors, construction work scheduling, understanding designs, and coordinating with all project stakeholders. This is a full-time position with a salary based on your prior experience (DOE). If you are detail-oriented, possess strong analytical skills, and have a background in billing engineering, we encourage you to apply and be part of our dynamic team at GUNNAM Infra projects.,

Job Description Candidate should have sound knowledge about upstream process development (Cell culture and Fermentation). Hands on experience of shake flask studies including sample analysis and documentation. Experience in handling and operation of cell culture and microbial related experiments in bioreactor including sample analysis and documentation. Aseptic handling of seed inoculum and its maintenance Independently handle media and feed preparation for conducting studies. Should be able to trouble shoot in case of any deviation from process/parameter. Good documentation practice. Should be able to perform cell culture (IPQC) analysis. Preparation of SOP, Support for Equipment qualification, Calibration pertaining to Upstream process as per laid down procedures Ensure quality compliance in Biotechnology Upstream laboratory as per Quality standards requirements

Are you passionate about leading and developing teams Do you thrive in a dynamic environment where collaboration and innovation are key If you are ready to take on a leadership role in a global organization that makes a real difference to patients" lives, we want to hear from you! Read on and apply today. As a Director in RA CMC Diabetes & Obesity, you will lead and develop a high-performing team, ensuring optimal employee development, planning, and resource utilization. You will set direction and implement a strategy for the team while fostering a culture of coaching, mentoring, and collaboration. Your responsibilities include overseeing people processes such as recruitment, development plans, performance evaluations, and succession planning. You will ensure compliance with quality, safety, and environmental standards, maintaining local QMS and adhering to regulatory requirements. Additionally, you will drive Business Scorecard (BSC) performance, ensuring clear target ownership and delivering results within deadlines. Your role involves developing the team and employees, driving people processes, and acting as a key stakeholder manager representing the team in local and global forums. You will ensure effective communication and collaboration across departments, internal stakeholders, and leadership teams such as RA CMC & Device LT. Furthermore, you will champion a cLean mindset, foster continuous improvement in work processes, represent RA CMC & Device in local initiatives, strategic projects, and cross-functional collaborations, and promote a mindset of collaboration and inclusiveness across departments in RA CMC & Device Bangalore. To thrive and succeed in this role, we would expect you to have a Master's degree in Lifesciences such as engineering, pharmacy, chemistry, or similar, along with 10+ years of relevant experience in the pharmaceutical industry working in a global regulatory function, manufacturing, CMC, QA, or a function collaborating closely with regulatory CMC. You should have 7+ years of proven leadership experience and a demonstrated ability to inspire, empower, and develop colleagues across geographies. Experience interacting with key stakeholders at a senior management level in production, CMC, production development, QA, and affiliates globally is required. Strong negotiating skills, clear communication, and comfort engaging with senior management are essential for this role. Overall, this position is right for you if you can consistently deliver on promises, set ambitious yet value-aligned goals, and solve complex challenges with a strong personal drive. You are authentic, honest, and can communicate effectively while inspiring and developing others through feedback and support. With a broad understanding of the NN value chain, you can make decisions for the greater good, share knowledge, and think beyond your own area. You can demonstrate resilience, challenge the status quo, reflect on feedback, build strong relationships, and have the courage to make tough decisions that benefit the organization. Join our team at Novo Nordisk, where we seek solutions that defeat serious chronic diseases. We approach our work with an unconventional spirit, rare determination, and a constant curiosity. Our unordinary mindset has seen us build a company unlike any other, where a collective passion for our purpose, mutual respect, and a willingness to go beyond what we know delivers extraordinary results. To submit your application, please upload your CV online by the 2nd of August 2025. Novo Nordisk is committed to an inclusive recruitment process and equality of opportunity for all job applicants.,

About Us Ethinos is a leading digital marketing agency with a strong presence in India and Australia. We specialize in crafting performance-driven, omnichannel campaigns across influencer marketing, social media, SEO, paid media, programmatic ads, automation, and web development. We blend data, creativity, and AI to deliver intelligent solutions that drive business outcomes. Website: www.ethinos.com Role Overview We re looking for an Influencer Outreach Manager who lives and breathes creators. Someone with a strong grasp of the influencer ecosystem across categories, platforms, and regions - and who knows how to turn influencer collaborations into ROI-driven success stories. This role will focus on identifying, onboarding, and nurturing long-term influencer partnerships while driving end-to-end outreach and collaboration for client campaigns. Key Responsibilities Influencer Outreach & Relationship Building Identify and onboard relevant influencers across categories for brand campaigns. Build and maintain strong, long-term relationships with macro and micro-influencers, creator agencies, and talent managers. Ensure alignment of influencer voice with brand values and campaign objectives. Train the inhouse influencer marketing team Pitch to the clients and maintain relationships Campaign Planning & Execution Collaborate with content, social media and video team to suggest the right influencer mix for each campaign. Negotiate contracts, manage deliverables, timelines, and payments. Oversee content quality, compliance, and adherence to brand guidelines. Performance Tracking & Reporting Track key metrics like reach, engagement, cost-efficiency, and ROI for each campaign. Analyse influencer content performance and generate insights for optimization. Prepare post-campaign reports for internal and client sharing. Industry & Platform Intelligence Stay up to date with platform algorithm changes, emerging influencer trends, and category shifts. Suggest new content formats, platforms (like Threads, Pinterest, Reddit, etc.), and creator opportunities. You Must Have 6 7 years of relevant experience, with at least 5 years in an influencer marketing agency . Strong understanding of influencer contracts, fee structures, and content rights. Hands-on experience working with creator databases, influencer marketing tools, and social media platforms. Excellent communication, negotiation, and relationship-building skills. Ability to handle multiple campaigns and clients simultaneously with high attention to detail. Bonus Points If You Have Managed large-scale influencer campaigns for fashion, lifestyle, F&B or BFSI brands. Experience working with creators on platforms beyond just Meta Prior experience in building influencer communities or ambassador programs.

The role of Team Lead involves overseeing and coordinating the daily activities of the PTL operations within the warehouse. You will be responsible for ensuring that all processes are carried out efficiently, safely, and in compliance with company policies. Your main duties will include supervising PTL operations, managing a team of associates, providing training and support, and driving continuous improvement initiatives. In terms of supervising PTL operations, you will need to oversee the daily activities of the PTL system to ensure accuracy and efficiency. Monitoring workflow and productivity, making adjustments as necessary to meet targets, and ensuring that all orders are picked accurately and on time will be crucial aspects of your role. As a Team Lead, you will also be responsible for leading, mentoring, and motivating a team of PTL associates. Conducting regular team meetings to communicate goals, updates, and provide feedback, handling scheduling, task assignments, and performance evaluations will be part of your responsibilities. In addition to team management, you will be required to provide training to new and existing employees on PTL processes and safety protocols. Identifying skill gaps and coordinating additional training as needed will also be an essential part of your role. Maintaining high standards of quality and accuracy in all PTL operations, ensuring compliance with health and safety regulations and company policies, as well as conducting regular safety audits and implementing corrective actions as needed are important aspects of this role. Furthermore, identifying opportunities for process improvements, collaborating with the operations manager to develop and execute improvement plans, utilizing data and metrics to drive performance and productivity enhancements will be key responsibilities. You will also be responsible for preparing and maintaining accurate records of daily activities, performance metrics, and incidents, as well as providing regular reports to the operations manager on key performance indicators (KPIs). To qualify for this position, a Bachelor's degree in logistics, supply chain management, or a related field is preferred. You should have 1-3 years of experience in warehouse operations, with at least 1 year in a supervisory or team lead role. A strong understanding of PTL operation and warehouse operations, excellent leadership, communication, and interpersonal skills, the ability to work in a fast-paced environment, and manage multiple priorities are essential. Strong problem-solving skills, attention to detail, and proficiency in Microsoft Office Suite and other relevant software are also required. This is a full-time position located in Wayanad, Kerala, requiring in-person work during day shifts. Health insurance is provided as a benefit. The ideal candidate will have at least 4 years of experience in logistics.,

Summary Professional experience in areas like Laboratory Management, Equipment Qualifications, Material management. This position may own & perform relevant System activities for a family of Drug Products and Sciences at R&D facility. Essential Duties and Responsibilities: As Lab Operator, responsible for equipment qualification (URS, DQ, IQ, OQ, PQ) for Formulation Lab equipment. Responsible for Periodic as well as daily, on-demand calibration and maintenance of formulation Lab equipment. Responsible for Maintaining all the PPE s protective gear, glassware and consumables for formulation activities and routine operations. Responsible for maintaining state of quality compliance in the lab as per global procedures including but not limited to lab procedures, documents, forms, lab data etc. Responsible for setting up the batch startup requirements before execution of scale-up batches in formulation Lab. Responsible for Material Planning & Handling before batch execution in Formulation Lab. Ensure good internal and cross-functional communication and regular status update of activities. Establish, maintain, and update Technical & Design documentation according to Good Documentation Practices. Ensure Quality & Compliance with Vantive policy/Ethics/Data Integrity and Environmental Health and Safety policies. Qualification: Diploma in Engineering discipline with minimum 5 years of experience, or Bachelor of Engineering discipline with minimum 3 years of experience or masters in science or Pharmaceutical discipline with minimum experience of 5 years as lab operator in pharmaceutical product development and life cycle management, preferably sterile injectable/parenteral formulations are preferred. Adequate knowledge of Equipment Qualifications and Laboratory management required for effective collaboration with cross-functions and execution of batches on time. Adequate knowledge of Lab Equipment s, Process, and Quality Management Systems. Adequate knowledge of international/regional/national regulations and standards. Demonstrates flexibility and the ability to shift gears between projects comfortably. Excellent oral and written communication skills. Good analytical and problem-solving skill. Good organizational skills. Ability to effectively organize and prioritize tasks.

Lead procurement, logistics, inventory & vendor management for solar projects. 8+ yrs in solar/renewables needed. Engineering degree required; MBA in SCM a plus. Based in Bangalore/Chennai. Drive efficiency & execution at Guna Solar.

Role Purpose The purpose of this role is to conduct audits to ensure quality compliance within the account. Do Conduct process quality audits as per plan Conduct various process audits (1 audit/ agent/ week) as per procedure and guidelines For agents identified in the bottom quartile of performance, conduct 3 audits/ agent/ week Prepare findings from the report and share it with the client and the account leadership on daily/ weekly/ monthly, as required Conduct weekly analysis to identify the error trends and for top 2 errors, conduct root cause analysis (RCA) Conduct calibration communication to communicate any changes from the client and conduct refresher trainings to bridge any skill gap due to these changes. Mandatory Skills: L&P Policy Acquisition & Servicing. Experience: 1-3 Years. >

Eurofins Consumer Product Testing India provides high standard quality assurance and control services, such as testing, certification, inspection, audits, technical and regulatory services, to manufacturers, brand owners, distributors and trading companies, buying associations, consumer associations, and retailers worldwide. We are dealing with various consumer product testing like: "¢ Fabric and Textiles "¢ Cosmetics "¢ Food contact materials "¢ Toys "¢ Detergents "¢ Apparel "¢ Rubber "¢ Leather "¢ Plastics "¢ Accessories "¢ Footwear "¢ Home Textiles With EUR 4.5 billion in annual revenues and 50,000 employees across over 800+ laboratories across 50 countries, Eurons Scientic is a leading international group of laboratories providing a unique range of analytical testing services to the pharmaceutical, food, environmental and consumer products industries and to governments. "¢ Should be a local candidate from Panipat. "¢ Knowledge of Home textiles products, like kitchen accessories / sheet sets / towels/ Mats etc. "¢ Relevant experience in QA/ QC (Quality Assurance/ Quality Control) "¢ Willing to travel. "¢ Maintain the quality compliance of the customers. "¢ To ensure product delivery on time to meet customer satisfaction. "¢ Should be able to handle day to day activities at production floors. "¢ To carry out all kind of controls/inspections like PPM, Inline, Mid, Final audits etc. as per AQL system & as defined by the buyer in order to get product in right desired quality within the given delivery date. "¢ Good computer and communication skills. "¢ Develop, manage implement, communicate, and maintain a quality plan to bring the Company"™s Quality Assurance Systems and Policies into compliance with quality system requirements. "¢ Effectively interact with the Technical, Development, and Production team to maintain product quality; ensuring that targets are achieved. "¢ Assisting technicians with checking patterns/specification and construction, identifying, and resolving production impracticalities in an appropriately timely manner, and to make a final decision on quality according to company standards and requirements. "¢ Supervise in the handling of sample evaluation and production approval by reviewing the measurement, workmanship, fitting, accessories, etc., and giving comments on the production. "¢ Monitored QA/QC performance by gathering relevant production data and producing statistical reports to be communicated with all related departments. Identifying relevant quality-related training needs and delivering training. "¢ Responsible for each aspect of TQM/Quality Management/Control and product assembly in the factory. "¢ Knowledge of problem-solving quality tools like fishbone, why-why analysis . "¢ Provide enough quality control seminars and coaching for company trainees. "¢ To conduct Risk Analysis and pre-production meeting and to give size set sample approval. "¢ Doing In-line inspection to check the quality/Follow up pre-Final / final inspections. "¢ To keep all necessary documents and quality SOP & ensuring all quality & production issue by Auditing & Controlling. "¢ To be able to provide approval such as print, embroidery, wash & as per required by the MR teams. "¢ To maintain all discipline and compliance issue & able to communicate with overseas customers. Qualifications "¢ Degree/Diploma in Textiles / NIFT graduate is preferred "¢ Minimum 10-15 years' relevant experience "¢ Strong knowledge of quality tools is a must "¢ Able to work under pressure, result oriented, excellent communication skills, self-motivated, responsive and detail minded "¢ Ability to build strong relationships with the team as a good team leader, communication effectively with internal and external parties "¢ Well organized individual, able to manage multiple tasks, strong problem-solving skills, handle multiple priorities in a fast paced and dynamic environment "¢ Excellent command of written and spoken English. Literate in Microsoft office programs If this sounds like you, ! Additional Information Key SkillQA manager, Quality Assurance home textile, Quality Assurance , quality control, ISO 17025 is must

Job Area: Engineering Group, Engineering Group > Quality Assurance Engineering General Summary: As a leading technology innovator, Qualcomm pushes the boundaries of what's possible to enable next generation experiences and drives digital transformation to help create a smarter, connected future for all. As a Qualcomm Software Quality Engineer, you will plan, implement, and manage compliance of Software development life cycle /manufacturing, production processes, and/or quality requirements with Quality managed , Functional Safety. Automotive Cybersecurity and regulatory standards for worldwide distribution. This role collaborates with various cross functional leads among the Automotive project team to ensure that product / process quality is met with set organization / customer expectations. Minimum Qualifications: Bachelor's Degree in Applied Science, Computer Science, Data Science, Engineering, Information Systems, or related field and 2+ years of Quality Engineering or related work experience. OR Master's Degree in Applied Science, Computer Science, Data Science, Engineering, Information Systems, or related field and 1+ year of Quality Engineering or related work experience. OR PhD in Applied Science, Computer Science, Data Science, Engineering, Information Systems, or related field. Automotive Software Quality - Staff Engineer - 10-14 years of experience in software process and product quality engineering - Proficient in automotive software quality compliance activities such as conducting audits/assessment - ensuring adherence to software product/process quality. - "Automotive SPICE- Provisional Assessor certification is must - Strong understanding of quality philosophies, principles, and methods. - Competent in data analysis - Recognizing patterns, data inference, drawing conclusions, deriving meaningful actions for issues found in the problem analysis - "Expertise in RCA, 8D is an advantage - Familiarity with tools like Jira, Codebeamer, Power BI, and Tableau. - Experience in automotive process definition and process improvement - "Experience in using AI driven tools to efficiently execute the SW quality activities Preferred - Minimum of 3 years of experience in software development. - Deeper understanding in process aspects of Cybersecurity and FuSa . - Experience in supplier / customer SW quality management - ASPICE Competent assessor **Summary of Responsibilities:** - Provide software product quality support for automotive software products. - Conduct internal ASPICE, Safety, and Cybersecurity audits to ensure conformance to ASPICE Requirements, ISO 26262, and ISO 21434. - Publish and track software quality metrics. **Preferred Soft Skills: ** - Excellent communication and interpersonal skills. - Persuasive and innovative mindset thinking, driving continuous improvement - Passionate execution - "Great teamwork skills Applicants Qualcomm is an equal opportunity employer. If you are an individual with a disability and need an accommodation during the application/hiring process, rest assured that Qualcomm is committed to providing an accessible process. You may e-mail disability-accomodations@qualcomm.com or call Qualcomm's toll-free number found here. Upon request, Qualcomm will provide reasonable accommodations to support individuals with disabilities to be able participate in the hiring process. Qualcomm is also committed to making our workplace accessible for individuals with disabilities. (Keep in mind that this email address is used to provide reasonable accommodations for individuals with disabilities. We will not respond here to requests for updates on applications or resume inquiries). Qualcomm expects its employees to abide by all applicable policies and procedures, including but not limited to security and other requirements regarding protection of Company confidential information and other confidential and/or proprietary information, to the extent those requirements are permissible under applicable law. To all Staffing and Recruiting Agencies Please do not forward resumes to our jobs alias, Qualcomm employees or any other company location. Qualcomm is not responsible for any fees related to unsolicited resumes/applications. If you would like more information about this role, please contact Qualcomm Careers.

Procurement Engineer - Fabrication Specialist Job Details | our company Search by Keyword Search by Location Select how often (in days) to receive an alert: Select how often (in days) to receive an alert: Procurement Engineer - Fabrication Specialist Functional area: Company name: Primax Pumps FZCO Date of posting: Jul 9, 2025 Our solutions are a key part of most industries - electronics, medical research, renewable energy, food production, infrastructure and many more. Working with us means working with the latest technologies and groundbreaking, sustainable innovations. Drive Fabrication Excellence for a Global Manufacturing Business! We are hiring a Procurement Engineer Fabrication Specialist based in Pune to lead the sourcing and development of suppliers for key fabricated components. You ll ensure our global manufacturing sites receive reliable, high-quality, and cost-effective materials. What you ll do: Source and qualify vendors for fabricated frames, panels, and structural parts Review and interpret engineering drawings and specifications Collaborate with internal teams to ensure technical and commercial alignment Negotiate with vendors to secure optimal pricing and lead times Monitor supplier delivery performance and quality compliance Support the resolution of fabrication-related quality issues Drive supplier improvements through audits and capability development You bring: An engineering degree (Mechanical/Industrial) Strong knowledge of welding, machining, and coatings A proactive approach to supplier engagement and performance Diverse by nature and inclusive by choice Bright ideas come from all of us. The more unique perspectives we embrace, the more innovative we are. Together we build a culture where difference is valued and we share a deep sense of purpose and belonging.

Responsibilities: * Collaborate with cross-functional teams on product development * Ensure compliance with regulatory standards * Conduct regular audits and inspections * Lead quality improvement initiatives Provident fund Annual bonus Health insurance

Role & responsibilities To review that all relevant quality management systems of Hosur manufacturing site are implemented and well maintained. To review, monitor and improve Quality performance of Hosur manufacturing site. To promote quality attitude, awareness, and mindset of the site by all proper means including training to the cross functional team members. Implement, audit, and develop quality management system, in line with Global quality policy/ manual and procedures relevant to area. Ensure the required process controls are in place wherever they are necessary. To review that testing and inspection of all raw materials, packaging materials and finished goods are carried out as per documented testing procedures and specifications. To review that the release of all raw materials, packaging materials, bulk as per approved SOP before they are used for further production activities. To review the release process of all finished goods as per approved SOP and global requirements including GFS before they are released for distribution. To review all RM and PM used in manufacturing process are from approved suppliers and with the required quality before it reaches Hosur manufacturing site including COA verifications against the documented specifications. To review all the internal lab/ External labs are conducting the testing processes as per the documented procedures and specifications. Ensure appropriate investigation are carried out throughout the manufacturing site in case of any quality related issue and ensure the corrective and preventive actions are implemented to mitigate the identified root causes for the quality issue. Ensure the preparation of training calendar and adherence to the same. To support and conduct self-inspection quality audits across all the QMS areas and continuously improve the QMS implemented at site. To ensure that all audit points/recommendations highlighted in the audit reports are followed up and closed effectively as per the agreed timelines. Review the performance of suppliers on a regular basis. To support all key initiative at the site as key member of the site. To support the site in conducting management review meetings as per the schedule. To accept and execute other responsibilities assigned by the management time to time.

Sample Inspection reports, experience in handling Instruments like vernier, Inspection of Fabrication Parts, Measurement Gauges, quality policies,Conduct tests as per SOP to verify the quality of finished products, Establish quality procedures Required Candidate profile Should have 3-4 years of experience working in QC, Should have basic knowledge of MS Office, Perks and benefits Permanent, Bonus, Paid Leaves Medical Insurance

The Quality Compliance Senior Manager plays a crucial role in the Clinical & Research Quality (CRQ) team for the R&D Quality Organization at Amgen. The CRQ team ensures that research and development activities are conducted ethically and responsibly, meeting the highest standards of quality and compliance to keep patients safe and protect their welfare. This position involves providing leadership to maintain excellence in R&D Quality Processes, mentoring Amgen staff in India, managing day-to-day activities, and ensuring compliance with regulations globally. Additionally, the Quality Compliance Senior Manager will support the digital quality management system (DQMS) and provide end-to-end quality support for managing Quality Incidents/Quality Events, including approving investigations and CAPA plans. Roles & Responsibilities: - Overseeing deviations, audits, and inspections across R&D Quality - Managing the Amgen India R&D Quality team - Facilitating deviation investigations and ensuring documentation within the electronic quality management system - Supporting Global Patient Safety and Global Development teams in inspection management activities - Leading continuous improvement initiatives for CAPA management practices - Collaborating with cross-functional partners to ensure effective processes aligned with industry best practices - Monitoring quality metrics, key performance indicators, and performing root cause trending - Maintaining knowledge of current regulatory and quality practices/issues - Managing archival and retention of audit documentation Basic Qualifications and Experience: - Masters degree with 10-12 years of Pharma and Biotech R&D or commercial manufacturing Quality experience - Continuous Improvement/Change Management experience preferred Additional Competencies/Skills: - Exceptional attention to detail and accuracy - Ability to work independently and proactively in a fast-paced environment - Proficiency in Smartsheet, Microsoft Office Suite, and virtual collaboration tools - Good team building skills and ability to develop employees over time - Familiarity with project management tools and methodologies - Knowledge of GCP, GLP, and/or GPvP - Experience working in a multinational environment - Excellent verbal and written communication skills - Strong problem-solving abilities and adaptability - Collaborative attitude and ability to build positive relationships across diverse teams Amgen ensures equal opportunities for individuals with disabilities throughout the job application process and employment. The company supports professional and personal growth through competitive benefits, a collaborative culture, and comprehensive Total Rewards Plans aligned with industry standards. Join Amgen to make a lasting impact on patient care and your career growth. Apply now at careers.amgen.com.,

Corporate Quality Assurance (CQA) Sr. Executive Posted: July 2025 Coral Drugs Pvt. Ltd. is seeking a skilled and experienced professional for the role of Senior Executive / Assistant Manager Corporate Quality Assurance (CQA). This position is ideal for candidates with over 7 years of experience, particularly within the Active Pharmaceutical Ingredient (API) sector. The role involves document review, audit processes, quality compliance, and regulatory adherence to global standards such as USFDA, EU-GMP, and WHO-GMP. Read more and apply

TL manual Testers with Wealth Management experience:Key Responsibilities:Test Plan Development:Creating comprehensive test plans and strategies based on project requirements and specifications. Test Execution:Conducting manual testing, including functional, regression, and performance testing. Defect Management:Identifying, documenting, and tracking defects using appropriate tools, and working with developers to resolve issues. Team Leadership:Supervising, mentoring, and guiding manual testers, ensuring they are properly trained and equipped to perform their duties effectively. Process Improvement:Identifying and implementing improvements to testing methodologies and processes to enhance overall quality. Compliance:Ensuring adherence to compliance and regulatory standards in wealth management applications. Communication & Collaboration:Collaborating with cross-functional teams, including developers, product managers, and business analysts, to clarify requirements and ensure project success. Reporting & Tracking:Monitoring and reporting on testing progress, risks, and issues, providing regular updates to stakeholders. Documentation:Maintaining accurate and up-to-date test documentation, including test cases, scenarios, and results. Environment Management:Managing testing environments and ensuring they are appropriately configured and updated.

ISRA VISON AG is looking for Procurement Engineer - Fabrication Specialist to join our dynamic team and embark on a rewarding career journey Analyzing customer needs to determine appropriate solutions for complex technical issues Creating technical diagrams, flowcharts, formulas, and other written documentation to support projects Providing guidance to junior engineers on projects within their areas of expertise Conducting research on new technologies and products in order to recommend improvements to current processes Developing designs for new products or systems based on customer specifications Researching existing technologies to determine how they could be applied in new ways to solve problems Reviewing existing products or concepts to ensure compliance with industry standards, regulations, and company policies Preparing proposals for new projects, identifying potential problems, and proposing solutions Estimating costs and scheduling requirements for projects and evaluating results

Role & responsibilities Own and drive the units full Profit & Loss (P&L) responsibility, ensuring financial sustainability and growth. Develop and execute annual budgets, cost optimization strategies, and revenue enhancement plans. Monitor and achieve financial KPIs including EBITDA, ALOS, BOR, and per-bed profitability. Should have handled a business of 100 plus crores Lead sales, marketing, and business development initiatives to expand patient base and service lines. Forge and maintain corporate, referral, and insurance tie-ups to boost revenue streams. Collaborate with the central marketing team to enhance brand visibility and patient engagement. Drive international patient programs, preventive health packages, and specialty clinics. Ensure efficient operations across all clinical departments (OP, IP, OT, ICU, diagnostics, pharmacy). Enable seamless coordination among departments for smooth, patient-centric service delivery. Ensure effective hospital information system (HIS) implementation and digital workflows. Monitor and improve clinical quality indicators infection control, readmission rates, patient safety, etc. Facilitate quality committees and implementation of clinical governance structures. Lead, motivate, and manage clinical and administrative teams to ensure alignment with hospital goals. Drive workforce planning, talent retention, performance management, and training initiatives. Cultivate a collaborative and ethical hospital culture focused on excellence and accountability. Oversee procurement efficiency and inventory control to maintain cost and service standards. Ensure uninterrupted utility services and readiness for emergency management protocols. Serve as the primary liaison with consultants, partners, statutory bodies, and local authorities. Handle regulatory reporting, legal compliance, and interface with government departments as needed. Represent the hospital in community outreach, media communication, and medico-legal matters. Preferred candidate profile Education: MBA in Hospital Administration / Healthcare Management (MBBS/PG in HA preferred). Experience: 15+ years in hospital leadership, including 5+ years in P&L-heavy roles in 200+ bed multispecialty or super-specialty hospitals. Proven record: Facility management, accreditation readiness, revenue growth, clinical quality. Interested candidates may also contact us directly at +91 99406 39536 for questions or more information.