409 Minitab Jobs - Page 17

Job Description mail:- info@naukripay.com Position: Quality Assurance (QA) Manager – Surgical & Medical Gloves Department: Quality Assurance Reports To: Director of Quality / Plant Manager Location: [Insert Location] Employment Type: Full-Time Job Purpose To lead and manage the quality assurance department, ensuring that all surgical and medical gloves produced meet regulatory, quality, and safety standards, and are in full compliance with ISO, FDA, ASTM, and other applicable standards. Key Responsibilities Quality Management System (QMS): Develop, implement, and maintain an effective QMS compliant with ISO 13485, ISO 9001, FDA 21 CFR Part 820, and other regulatory standards applicable to medical device manufacturing. Regulatory Compliance Ensure that products meet all regulatory requirements including FDA, CE marking, ASTM standards, and other local/international certifications. Process Control & Improvement Monitor production processes to ensure product quality and consistency. Lead process validation, CAPA, risk management, and root cause analysis efforts. Inspection And Testing Oversight Supervise incoming, in-process, and final product inspection and testing activities. Ensure all gloves meet defined specifications for physical, chemical, and microbiological attributes. Internal And External Audits Plan and lead internal audits; coordinate with external auditors and regulatory authorities during inspections and audits. Address non-conformities with corrective/preventive actions. Documentation And Reporting Maintain accurate QA documentation, including batch records, test reports, deviation reports, and audit findings. Generate monthly quality performance reports for senior management. Team Leadership Lead, mentor, and train QA staff to ensure continuous development and adherence to quality standards and procedures. Customer Complaint Handling Investigate and resolve quality-related customer complaints. Implement improvements to prevent recurrence. Supplier Quality Assurance Evaluate and audit suppliers of raw materials to ensure incoming goods meet quality requirements. Qualifications And Skills Bachelor’s degree in Chemistry, Microbiology, Biomedical Engineering, or a related field. Master’s preferred. Minimum 5–8 years of experience in quality assurance within a medical device or glove manufacturing industry. In-depth knowledge of international regulatory standards (ISO 13485, FDA, ASTM, EN). Strong analytical, problem-solving, and leadership skills. Excellent communication and interpersonal skills. Proficient in MS Office, QMS software, and statistical tools (e.g., Minitab). Requirements Must be a high school graduate. Further training in child care and development from some registered institution (eg. ACNS ). Proven child care experience with references. First Aid and CPR certification. Safety certification. A valid driving license and a safe driving record.

Division ALIDAC QA Job posted on May 12, 2025 Employee Type P-P7-Probationer-HO Staff Experience range (Years) 5 years - 10 years ZTMP – REQUEST FORMAT Name : Garima Jha BU : Quality Place : ZLL-SEZ Oncology Injectable, SEZ, Matoda, Ahmedabad. Contact # : 9173639189 Email Id : Garima.G.Jha@ZydusLife.com Basic Details: Position : Senior Executive Designation : Senior Executive Reports to : Associate Manager Department : Quality Assurance Location : ZLL-SEZ Oncology Injectable (Alidac) No of Posts : 1 Role : Critical Neev Level : 1 Details : Replacement Position code : 60055060 Position Name : Senior Executive Key Job Description: (Not more than 5 points in 6 lines) QA-QMS Role - To perform investigation of Deviation, Market complaint, Adverse Drug Events, Alert notification and product failures as per approved procedure. To ensure proper justification for the change proposed with its impact analysis, risk assessment and effectiveness check with its acceptance criteria. To complete the preliminary investigation and final investigation report within stipulated time. To do document historical check with inference by examining relevant data sources with respect to the nature of the event. To use appropriate investigation tool for investigation. To collect circumstantial evidence and considering for investigation. To interview personnel involved if needed in such a way that its relevant and adequate to identify cause. To review batch records & relevant records and identify the indicators of an event. To identify the root cause based on investigation outcome. To perform vertical and horizontal impact assessment based on the root cause. To coordinate with cross functional team for immediate action which may be deemed necessary to isolate the event, to limit any adverse effect on production, materials, equipment, areas, processes, procedures including discontinuation of processing or quarantine. To coordinate with contract givers for alert notification filing to the Agency, if applicable. To derive on appropriate CAPA in consultation with CFT for the event with a justifiable target completion date. To determine appropriate CAPA effectiveness plan. To Handle the Change control and check the effectiveness of the proposed change. To prepare, execute and review of Process Validation and Cleaning Validation. To prepare and review SOP’s in documentum software against current regulatory guidance. To do trend analysis of QMS (Change control, deviations, CAPA, market complaints, FAR, and Product recall ). To participate in Regulatory audit/ Customer audit and its compliance. To do trend analysis of repetitive issues. To discuss outcomes of trend analysis with the QA head and suggest appropriate CAPA. To have a focus on the investigation to get the consistency for improving the quality of investigation. To evaluate the change for its impact and recommend actions based on the change, to identify any additional members required for evaluation based on the change proposed. To maintain online entries in ZyQMS. To maintain APQR calendar/ schedule. To prepare and review the APQR. To monitor and prepare CPP report of product through validator and Minitab software. To prepare and review the visual inspection rejection trend in Minitab software. Requirements: Qualification : M.Pharm Years of Experience : 5 to 10 years Experience in Zydus : 2 years Experience / Exposure in (2 points) : Must have knowledge and experience in injectable plant. Mail your CVs to: Garima.G.Jha@ZydusLife.com/HardikA.Bhatt@ZydusLife.com

JUNTOS SOMOS BALL Ball Corporation es una compañía que ofrece igualdad de oportunidades. Alentamos activamente las solicitudes de todos, independientemente de su género, edad, etnia, religión, habilidad u orientación. Cuando te unes a Ball, perteneces a un equipo de más de 22.000 empleados en todo el mundo. Hacemos desde latas, vasos y envases de aerosol de aluminio infinitamente reciclables, que permiten a nuestros clientes tener una comprensión más profunda de nuestro planeta y el universo. Cada uno de nosotros tiene un profundo compromiso con la diversidad y la inclusión, que es la base de nuestra cultura de pertenencia. Todos en Ball estamos marcando la diferencia al hacer lo que amamos. Porque lo que creamos puede cambiar, pero lo que siempre haremos es la diferencia. JUNTOS, QUEREMOS CONSTRUIR UN FUTURO SUSTENTABLE, PARA ESO... Buscamos un(a) Analista de Procesos que será responsable de desarrollar, analizar, controlar e implementar mejoras en los procesos de fabricación, a través del uso y desarrollo de metodologías y herramientas de gestión, con el objetivo de optimizar, estabilizar y estandarizar los procesos y la capacitación de los empleados. PARA JUNTOS ALCANZAR LO EXTRAORDINARIO, SERÁS RESPONSABLE DE: Asegurar la estandarización de los procesos de fabricación, a través de la elaboración, revisión y verificación del cumplimiento de los procedimientos operativos, a fin de minimizar las variaciones en los procesos. Participar en el desarrollo de materiales de capacitación sobre el proceso de fabricación, contribuyendo a la difusión del conocimiento dentro de la fábrica. Monitorear el consumo de las entradas principales a través de sistemas computarizados y datos de campo, con el objetivo de señalar tendencias desfavorables, proporcionando a los gerentes información para la toma de decisiones. Monitorear el deterioro y el rendimiento del equipo de todo el proceso de fabricación a través de sistemas computarizados y datos de campo, así como analice la información, señale e implemente mejoras e interactúe con el equipo de producción en busca de mejores resultados. Participar en eventos Lean (SMED, Kaizen, proyectos 6 Sigma, etc.), con el objetivo de reducir el consumo de insumos y el deterioro, así como mejorar el rendimiento del equipo. Coordinar una de las herramientas de Lean, dirigiendo actividades, con el objetivo de contribuir a la difusión de la cultura de mejora continua en la Unidad. Monitorear el deterioro y el rendimiento del equipo durante todo el proceso de fabricación a través de sistemas computarizados y datos de campo, así como analice la información, señale e implemente mejoras e interactúe con el equipo de producción en busca de mejores resultados. Aprender las actividades de producción, calidad o supervisores, mediante la vigilancia rutinaria, con el objetivo de formar a sí mismos para llevar a cabo estas funciones en situaciones específicas y sucesión. Mantenga el área de trabajo y el equipo limpios y organizados de acuerdo con las buenas prácticas de fabricación y las herramientas 5S, utilizando y alentando a otros empleados en el lugar de trabajo a adoptar herramientas Lean y resolver las no conformidades detectadas en auditorías para optimizar procesos, evitar accidentes y contaminación del producto. PARA QUE JUNTOS HAGAMOS LA DIFERENCIA, ESPERAMOS QUE TENGAS: Graduación universitaria preferiblemente en Ingeniería, Química Industrial, Tecnología o Administración de Empresas. Paquete de Office, con Excel avanzado (Deseable). Proyecto MS y Minitab (Deseable). Inglés - nivel intermedio (Deseable). Requisitos ISO 9001, ISO 14001, ISO 22000 y ISO 45000 (Deseable). Herramientas de Lean Manufacturing (Deseable). Herramientas de calidad y control estadístico de procesos (Deseable). INFORMACIONES ADICIONALES: Lugar de trabajo: Guarambaré, Paraguay. Modalidad: Presencial JUNTOS PODEMOS SER MÁS Desarrolle su carrera en Ball, líder mundial en la fabricación de envases de aluminio sostenibles. ¡Logra cosas extraordinarias al unirte a nuestro equipo y marca la diferencia en tu desarrollo profesional, en la comunidad y en todo el mundo!

- 1+ years of tax, finance or a related analytical field experience - 2+ years of complex Excel VBA macros writing experience - Bachelor's degree or equivalent - Experience defining requirements and using data and metrics to draw business insights - Experience with SQL or ETL Do you enjoy solving complex business problems, transforming data into information, and using that information to influence business decisions? Are you able to form a picture and tell a story based on what the numbers are saying? Do you have experience joining data sets from disparate sources in order to do so? If so, this opportunity may be for you. Are you interested in being part of a high visibility, strategic team that directly impacts Amazon worldwide? The IN-AMXL Supply Chain team is looking for motivated self-starters that can work in a fast paced, data-driven environment. The successful candidate will be an analytical problem solver, have an extremely high level of customer focus and a passion for process improvement. As you launch your career as a Business Analyst at Amazon, you will focus on improving the success within Operations fulfillment by analyzing data, discovering and solving real world problem, and building metrics and business cases to improve the customer's experience. The responsibilities include, but not limited to: • Identify and build data sources • Extract, manipulate, assess, maintain data quality and convert data to facilitate and conduct analysis Key job responsibilities • Enable effective decision making by retrieving and aggregating data from multiple sources and compiling it into a digestible and actionable format • Partnering with other analysts and BI engineers in planning and analytics to build analytical solutions to deliver on business goals • Propose and implement business metrics for senior management reviews and work with business intelligence and data engineers to design and develop data infrastructure to support business growth • Perform deep-dives to find the root causes behind variances of key parameters over a given time-period • Harness data to create business requirements documents and guide actionable technology requests • Collaborating with cross-functional teams, including finance, supply chain execution, transportation, and others, to identify pain points and opportunities for optimization. • Conducting in-depth analysis and cost-benefit assessments to evaluate the feasibility and impact of potential initiatives. • Program manage projects with category teams and drive decision making across cross functional teams and senior leadership acting as a common link between operations and categories. About the team The IN-AMXL Supply Chain is responsible for forecasting the volumes on weekly basis for OB, IB, Customer returns, Trans in and Trans out flows (upto 8 weeks). We also own the inventory replication across the network. Our Forecasting and planning teams work with cross functional collaboration to ensure all possible future external as well as internal factors are taken into consideration while forecasting so that we have the highest accuracy reducing site level churn and increasing efficiency. All flow owners monitors the flow of packages with respect to forecast on daily basis using S&OP deck and take appropriate actions on ground if we see high deviation in volume in comparison to plan which in turn ensure there are no choke points and prevents high backlog on floors which leads to good Customer experience. Internal job description Please provide resume and work samples. To apply for this role, candidates must initiate an informational meeting with the hiring manager by clicking the "Request Informational" button at the top of the job listing.. For more on informational discussions, visit: https://ivy-help-center.talent.a2z.com/article/2gLzMFp5I3TMfchHDv03w2?ref=share-button To understand the internal transfer process and frequently asked questions, refer to: https://ivy-help-center.talent.a2z.com/article/5TdnwN6zJXjHvREhjtTdAJ?ref=share-button Loop competencies -- Basic qualifications - 2+ years of Excel or Tableau (data manipulation, macros, charts and pivot tables) experience - Bachelor's degree or equivalent - Experience defining requirements and using data and metrics to draw business insights - Experience creating complex SQL queries joining multiple datasets, ETL DW concepts - Experience in Excel (macros, index, conditional list, arrays, pivots, lookups) - Experience scripting for automation (e.g., Python, Perl, Ruby) - Experience using Python or R for data analysis or statistical tools such as SAS - Experience using statistical tools such as Minitab - Experience with reporting and Data Visualization tools such as Quick Sight / Tableau / Power BI or other BI packages - Experience in project management Preferred qualifications - Experience using very large datasets - Experience using hard data and metrics to back up assumptions and concepts - Experience in leading internal program/sprints to align priorities with planners within the team and ensure on-time delivery. Experience working with Tableau Experience using very large datasets Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit https://amazon.jobs/content/en/how-we-hire/accommodations for more information. If the country/region you’re applying in isn’t listed, please contact your Recruiting Partner.

ABOUT AGRATASAgratas is a wholly owned subsidiary of Tata Sons. We design, develop and manufacture high-quality, high-performance, sustainable batteries applied to multiple use cases in the mobility and energy sectors, to match our customers’ requirements. Agratas is a scale-up business with a start-up mentality, driven by our pursuit of green growth and technological progress. We develop next-generation battery technologies at our state-of-the-art R&D Innovation Hubs in India and the UK. ROLE PROFILEThe OpportunityWe are seeking a technically skilled and detail-oriented Process Engineer to lead web handling and tension control systems within the electrode coating process of our Li-ion cell manufacturing line. The candidate will be responsible for designing, optimizing, and troubleshooting web transport systems to ensure coating quality, edge alignment, and film integrity throughout the coating section. Business Expertise:Requires understanding of manufacturing operations, quality systems, and how different departments (like R&D, supply chain, and maintenance) work together. Knowledge of industry trends and competitor technologies is essential.Problem Solving:Deals with complex issues such as process variability, yield loss, and equipment reliability. Requires analytical thinking, innovation, and adaptability to environmental factors like humidity and material behavior.Nature & Area of Impact:Directly impacts production efficiency, quality, and cost. Influences the performance of teams and departments, contributing to business goals and overall competitiveness. PERSON PROFILEKey Accountabilities and ResponsibilitiesProcess Design & Optimization Design and optimize web handling systems for uniform coating on electrode foils (Al & Cu).Define and validate tension profiles across different coating zones: unwinding, coating, drying, rewinding.Optimize parameters for web speed, roller alignment, nip pressure, and dynamic tension compensation.Control Systems & Automation Develop and fine-tune closed-loop tension control systems using load cells, dancers, brakes, and servo drives.Work with automation engineers to integrate PLC/SCADA/HMI for real-time monitoring and control.Ensure synchronization across multiple web zones (e.g., dual-sided coating, segmented dryers).Coating Quality & Web Stability Prevent web defects such as wrinkles, misalignment, telescoping, and flutter.Maintain coating uniformity by ensuring consistent web tension and speed during dynamic operation.Analyze the impact of web tension on slurry coating behavior and drying consistency.Scale-up & Equipment Commissioning Support commissioning and ramp-up of new coating lines and upgrades.Collaborate with OEMs on web path design, tension control logic, roller selection, and automation integration.Maintenance, Monitoring & Troubleshooting Develop standard operating procedures for tension control systems.Perform root cause analysis and resolve issues related to web breakage, coating defects, or tension instability.Conduct periodic calibration and maintenance of load cells, encoders, and web guide systems.Documentation & Cross-functional Support Document tension control strategy, process settings, and alarm logic.Interface with quality, maintenance, and R&D teams to align web handling design with product requirements and experimental trials.Knowledge, Skills and Experience EssentialDesign and refine web transport systems to ensure smooth movement of electrode sheets during coating, drying, and winding stages without defects or misalignment.Maintain precise control of web tension throughout the process to prevent issues such as wrinkles, breaks, or misregistration, ensuring consistent product quality.Hands-on experience in tension control systems, servo drives, web guiding, and dynamic roller systems.Strong understanding of mechanics of continuous webs, foil deformation, and process-material interaction.Proficient with tools like AutoCAD, SolidWorks, and control system platforms (e.g., Siemens, Allen Bradley).Use sensors, load cells, and control software to continuously monitor tension and alignment, and make real-time adjustments for optimal performance.Identify and resolve process abnormalities such as web drift, telescoping, or slack zones to minimize downtime and material waste.Ensure web handling components like rollers, brakes, tension controllers, and guiding systems are properly maintained and calibrated for reliable operation.Work closely with coating, maintenance, and automation teams to integrate and improve web handling strategies in line with production goals. DesiredDeep understanding of web handling mechanics, including tension zones, nip points, speed differentials, and dancer/feedback control systems.Proficiency with PLCs, HMI interfaces, and closed-loop control systems used for web alignment and tension regulation.Experience with data analysis and process control tools (e.g., SPC, Minitab) to monitor performance, identify trends, and implement corrective actions.Familiarity with process data acquisition and analysis tools to monitor web performance and drive continuous improvement.Strong communication and cross-functional collaboration skills to work effectively with R&D, quality, and production teams.Role Specific Qualifications/CertificationsBachelor’s or master’s degree in chemical engineering, Materials Science, Mechanical Engineering, or a related field3-10 years of experience in a manufacturing environment, preferably in battery, chemical, or pharmaceutical industries.

Roles and Responsibilities To participate and prepare/ review Computer System Validation and IT-QMS documentation To implement automation at site in coordination with IT, CSV, and user departments To implement software at site i.e. Labware LIMS, SAP, e-QMS, e-DMS, e-LMS, Minitab, e-BMR, Lab-solution, Empower etc. To perform / participate in qualification / periodic qualifications of software at site To prepare compliance documents preparation against observations related to computer systems To participate / perform self-inspections / internal audits at site To prepare SOPs in Quality Assurance Department To involve in Regulatory audits/customer audits for the compliance of Software & IT systems at site. To participate in qualifications of IPC/ SCADA, PLC, HMI system based equipment. To participate in qualifications/calibration of system connected / standalone instruments in laboratory. To perform GAP assessment of computerized system with respect to regulatory and current requirements in GMP To perform and review Data Backup, Verification and Restoration in GxP systems. To perform / review Preventive Maintenance of GxP system software. Skills & Knowledge Required in Candidate Sound knowledge in automation / Software implementation in the pharmaceutical industry Management of GxP automation activities and compliance at site. Good communication and interpersonal skills EU/ TGA/ ANVISA regulatory audit exposure is an advantage Good knowledge of European agency guidelines & GAMP guidelines Well-versed with EU Annex 11 / 21 CFT Part 11 guidelines Sound knowledge of ALCOA+ concepts and able to identify gaps w.r.t. ALCOA+ principles if any in software implemented at site Preference if any The candidate is required to be present at the site by JULY 2025.

Long Description • Define productivity metrics and align operating definitions with QC teams. • Simplify and digitize data for reporting QC productivity metrics. • Publish monthly QC productivity metrics reports for all labs. • Identify improvement levers for QC productivity and develop action plans to address them, reporting progress regularly. • Manage projects and track the deployment of new technology in QC. Technical/Functional Skills: • Hands-on experience in operations, with a strong understanding of Lean Manufacturing methodologies. • Proficient in data analysis using Excel/Minitab. • Proven track record of executing high-value projects. Competencies Developing Talent Innovation & Creativity Result Orientation Strategic Agility Process Excellence Customer Centricity Collaboration Stakeholder Management Education Masters in Business Administration Graduation in Biopharmaceutics 6 - 8 Years of Work Experience

We are Lenovo. We do what we say. We own what we do. We WOW our customers. Lenovo is a US$57 billion revenue global technology powerhouse, ranked #248 in the Fortune Global 500, and serving millions of customers every day in 180 markets. Focused on a bold vision to deliver Smarter Technology for All, Lenovo has built on its success as the world’s largest PC company with a full-stack portfolio of AI-enabled, AI-ready, and AI-optimized devices (PCs, workstations, smartphones, tablets), infrastructure (server, storage, edge, high performance computing and software defined infrastructure), software, solutions, and services. Lenovo’s continued investment in world-changing innovation is building a more equitable, trustworthy, and smarter future for everyone, everywhere. Lenovo is listed on the Hong Kong stock exchange under Lenovo Group Limited (HKSE: 992) (ADR: LNVGY). This transformation together with Lenovo’s world-changing innovation is building a more inclusive, trustworthy, and smarter future for everyone, everywhere. To find out more visit www.lenovo.com, and read about the latest news via our StoryHub. Job Description As a Quality Assurance Specialist, you will be a critical part of our organization’s commitment to delivering top-notch products and services. Your meticulous attention to detail and analytical mindset will ensure that our offerings meet the highest quality standards. Here’s a comprehensive breakdown of your responsibilities: Responsibilities Developing and Implementing Quality Assurance Strategies: Collaborate with cross-functional teams to create robust quality assurance policies and procedures.Establish guidelines for product development, testing, and release processes. Product Inspection And Testing Perform rigorous quality tests, including functional, performance, and reliability assessments.Identify defects, deviations, and areas for improvement. Root Cause Analysis And Corrective Actions Investigate quality issues and determine their root causes.Propose corrective and preventive actions to enhance product quality.Collaborate with production and engineering teams to implement necessary changes. Process Audits And Compliance Conduct regular process audits to ensure adherence to quality standards.Monitor compliance with industry regulations, safety protocols, and best practices.Maintain accurate documentation of audit findings. Supplier Quality Management Evaluate and qualify Vendors based on quality criteria.Collaborate with vendors to improve their processes and product quality.Monitor Vendor performance and address any quality-related issues. Continuous Improvement Initiatives Drive continuous improvement efforts across the organization.Implement quality control tools such as Six Sigma, Lean, or Total Quality Management.Foster a culture of quality consciousness among team members. Training And Skill Development Develop training programs for employees involved in quality assurance.Keep the team updated on industry trends, emerging technologies, and best practices. Data Analysis And Reporting Collect and analyze quality data using statistical methods.Generate comprehensive reports on quality metrics, defect rates, and trends.Present findings to management and recommend actionable insights. Requirements And Skills Experience and Qualifications:Bachelor’s degree in a relevant field (e.g., Quality Management, Engineering, or related discipline).Proven work experience in quality assurance or a related role.Certifications such as Certified Quality Auditor (CQA) or Certified Quality Engineer (CQE) are advantageous.Technical Competencies:Proficiency in quality management systems (ISO 9001, ISO 13485, etc.).Familiarity with quality tools (FMEA, Control Charts, Pareto Analysis, etc.).Knowledge of statistical analysis software (e.g., Minitab, JMP).Soft Skills:Excellent communication skills (both written and verbal).Strong problem-solving abilities.Attention to detail and a commitment to precision.Ability to work collaboratively in a team environment.Education - GraduateWorking Days - 6 days We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, religion, sexual orientation, gender identity, national origin, status as a veteran, and basis of disability or any federal, state, or local protected class.

*General Duties:* Work as an ISO & Management Consultant. We seek an ISO & Management Consultant to help organizations implement and maintain management systems, ensuring compliance with international standards (ISO 9001, ISO 14001, ISO 45001, etc.). The ideal candidate will possess excellent consulting, auditing, and project management skills. *Job Responsibilities:* · Conduct gap analyses and assessments for ISO implementation. · Develop and implement management systems (QMS, EMS, OHSMS, etc.). · Provide training and awareness sessions for clients. · Conduct internal audits and management reviews. · Identify areas for improvement and recommend solutions. · Develop and maintain ISO-compliant documentation (policies, procedures, etc.). · Establish and maintain quality, environmental, and health & safety management systems. · Ensure compliance with ISO standards and regulatory requirements. · Conduct risk assessments and develop mitigation strategies. · Conduct internal and external audits (ISO 9001, ISO 14001, ISO 45001, etc.). · Identify non-conformities and provide corrective action recommendations. · Evaluate audit findings and report to clients. *Required Skill & Qualifications:* · Required Skill as Self-motivated with proven leadership skills, Proficient in Microsoft Office, Prior experience in food environment, Must be able to work in a team environment, Must have a positive attitude, Ability to work in fast-paced, effectively under pressure. · Experience: Minimum 1-2 Years in any Industry in Quality Control. · Must have detailed knowledge about Management Certification requirements. · Knowledge of industry-specific regulations and standards · Familiarity with consulting tools and software (e.g., Minitab, Excel) · Ready to travel across country as per company requirements.