5 Nonconformance Management Jobs

As an SAP PPQM Consultant, you will be responsible for facilitating the implementation and support of SAP Production Planning (PP) and Quality Management (QM) modules. Your role will involve performing detailed analysis of complex business process requirements, identifying customer needs, and providing appropriate system solutions. You will also be required to facilitate workshops to gather business requirements, map client processes, and develop necessary product modifications to meet client objectives. In addition, you will design, customize, configure, and test SAP PP and QM, identifying gaps and proposing work-around solutions as needed. You will act as a liaison with clients for troubleshooting software problems, document functional designs and test cases, and proactively identify business process enhancements. Furthermore, you will provide consulting services for new implementations and support projects, serving as a bridge between business functions and technical teams. Desired skills and experience for this role include a minimum of 3+ years of experience in designing and configuring the PP-QM module, with strong knowledge in SAP Production Planning and Quality Management Modules. SAP certification in Production Planning and Quality Management is desirable. You should have worked on at least 2 full project life cycle implementations with SAP PP and QM modules, along with support projects. Moreover, you should have good integration knowledge with other components such as CO, MM, and SD, and have experience in Discrete, Process Industries, and Repetitive Manufacturing scenarios. Familiarity with Sales and Operational Planning, Long-Term Planning, Material Requirement Planning, Demand Management, capacity evaluation, and production execution processes is essential. Additionally, strong knowledge of Planning strategies (Make to Order/Make to Stock/Engineer to Order), Quality Planning, Quality Inspection, Quality Improvement processes, and table relationships will be advantageous. You should have the ability to multitask, manage multiple projects simultaneously, understand business processes from a customer perspective, and effectively collaborate in a team environment. Previous experience in a Core industry and SAP certification are preferred. Qualifications required for this role include a B.E/B.Tech/MBA degree. If you meet these qualifications and have the desired skills and experience, we encourage you to apply for this position.,

The Quality Control Head is responsible for overseeing the quality assurance and quality control processes in construction projects. You will be required to develop, implement, and maintain a Quality Management System (QMS) to ensure compliance with industry standards, regulations, and client specifications. This role involves establishing quality objectives, policies, and procedures, supervising inspection and testing activities, conducting site inspections, and audits, maintaining detailed records, preparing quality reports, and managing non-conformances. Additionally, you will be responsible for developing corrective and preventive action plans, training staff on quality standards, evaluating suppliers and subcontractors, ensuring compliance with building codes and safety regulations, and communicating effectively with clients to ensure satisfaction. Qualifications required for this role include a Bachelor's degree in Civil Engineering, Construction Management, or a related field (Master's degree is a plus), professional certifications such as Certified Quality Engineer (CQE) or Project Management Professional (PMP), and a minimum of 15 years of experience in quality control/assurance in the construction industry. Strong knowledge of construction methods, materials, regulations, excellent analytical and problem-solving skills, leadership abilities, and effective communication skills are essential. Key skills for this role include strong mathematical and analytical abilities, attention to detail, communication skills, teamwork, problem-solving skills, and physical stamina to work on construction sites in various weather conditions. The position may involve both office work and on-site inspections, travel to construction sites, and the ability to work in a fast-paced environment. Opportunities for career advancement include senior management positions such as Quality Assurance Director, Construction Manager, or Operations Manager. Continued professional development and certification in quality management and construction practices are encouraged. To apply for this position, please share your resume at hr@dhinwaconstruction.com along with a brief note on why you are a good fit for the role. Kindly use "Application for Quality Assurance and Quality Control Head" as the subject line of the email and mention your current CTC and notice period.,

As a Lead QMS at Ai Health Highway, you will play a crucial role in implementing Quality Management System (QMS), ISO13485, EU MDR, and US FDA (510k) Risk Management processes for our cutting-edge medical devices. Your responsibilities will include creating device master records, updating technical documentation, and collaborating with internal and external stakeholders to establish a robust quality management and regulatory framework for our product pipeline. You will work closely with engineering and manufacturing teams to develop verification test strategies to ensure the safety and reliability of our products. Additionally, you will be involved in developing product requirements, supporting validation programs for new product development, and providing inputs for regulatory guidelines and procedures. Your expertise in risk assessment for medical devices, as per ISO13485/ISO 14971 CE certification, will be essential in this role. You will also be responsible for reviewing device labelling and advertising materials for compliance with regulations, liaising with external consultants, and assisting in documentation preparation for US FDA (510k) and EU-CE Marking regulatory submissions. To be successful in this position, you should have 3 to 5 years of experience in the Medical Device QMS and regulatory domain, along with a BTech/BE in Electronics/Electrical/CS or Bio-Medical Engineering. Strong skills in documentation, review, reporting, and excellent interpersonal communication are required. Experience in managing non-conformance, corrective action preventive actions, deviation, and conducting QMS training will be beneficial. Join us at Ai Health Highway in our mission to reduce premature deaths due to Non-Communicable Diseases by 30% by 2030. Your expertise and dedication will contribute significantly to our goal of revolutionizing healthcare with innovative medical devices.,

The Senior QA Executive plays a crucial role in overseeing various aspects of quality management within the organization. This includes but is not limited to document control, compliance monitoring, internal audits, quality metrics tracking, and non-conformance management. The position also involves contributing to change control, supplier evaluation, risk management, product and process validation, complaint handling, CAPA support, and quality improvement projects. A key part of the role is to engage in data entry, analysis, and report preparation to ensure alignment with quality and compliance objectives. Responsibilities of the role include: - Document Control: Assisting in the organization and maintenance of quality documentation such as the Quality Manual, Documented Procedures, Standard Operating Procedures (SOPs), and forms. - Internal Audits: Participating in internal audits across various departments to evaluate compliance with the Quality Management System (QMS) and providing reports to senior QA staff. - Non-Conformance Management: Supporting the investigation of non-conformities or deviations, including root cause analysis and the development of corrective and preventive actions (CAPAs). - Change Control Support: Aiding in the change control process by reviewing change requests and assessing their impact on quality and compliance. - Risk Management Assistance: Collaborating with senior QA staff to conduct risk assessments and implement risk management strategies. - Product and Process Validation Support: Participating in activities related to product and process validation to ensure they meet specified requirements. - Complaint Handling Support: Assisting in the review and resolution of customer complaints pertaining to product quality. - Corrective and Preventive Action (CAPA) Support: Supporting CAPA processes by collecting data and monitoring the progress of corrective actions. Candidates for this role are expected to have a Bachelor's or Master's degree in a life science background and ideally possess 2 to 4 years of relevant experience in a similar role within the IVD industry. Interested candidates are encouraged to share their CVs with hr2@athenesedx.com to be considered for this position.,

Your responsibilities will include collaborating with manufacturing teams to address customer-specific quality requirements and analyzing customer feedback for areas of improvement. You will assist in maintaining quality management systems, including updating procedures and quality documentation. Participation in risk assessment activities such as failure mode and effects analysis (FMEA) will be required, along with contributing to the development of risk mitigation strategies. You will also set up efficient change management processes and regularly update risks based on reported non-conformities and process enhancements. Conducting routine inspections and audits of manufacturing processes, materials, and products to identify quality issues will be part of your role. Additionally, you will support the analysis of process performance data and generate reports to facilitate decision-making and continuous improvement efforts. Managing non-conformities by raising Non-Conformity Reports (NCR), documenting measurements, and supporting root cause analysis will also be essential. You will participate in cross-functional teams to drive continuous improvement initiatives and enhance manufacturing process performance. Your role will involve systematically identifying and addressing root causes of problems, managing risks, and handling conflicts effectively. Emphasizing continuous improvement, you will challenge the status quo, implement change within the workplace, and develop processes for consistent results. Living by Hitachi Energy's core values of safety and integrity will be crucial, taking responsibility for your actions, caring for colleagues, and upholding business values. To qualify for this position, you should have a Diploma in Mechanical Engineering and 2 to 4 years of experience in the Quality field, preferably with the same type of switchgear product. Proficiency in quality management systems, auditing processes, PFMEA, process design and optimization, and spoken and written English is required. If you are seeking an entry-level role in Quality Management and possess the necessary qualifications and skills, we encourage you to apply now for this full-time position based in Maneja, Gujarat, India.,