4 Capa Processes Jobs

Job Description Your role: Provides range of supporting activities to environment, health and safety team to ensure tasks are completed efficiently and effectively, exercising autonomy within established procedures. Performs periodic safety inspections, monitoring hazardous waste removal vendors, and may assist in consolidating hazardous wastes (chemical, radioactive, and/or medical). Maintains a detailed inventory of all safety equipment, tracking usage, maintenance schedules, and replacement dates to ensure that resources are always available and in optimal condition. Investigates workplace accidents and incidents, analyzing root causes, and preparing reports with actionable recommendations aimed at preventing future occurrences. Identifies, evaluates and utilizes administrative tools to improve health and safety processes, regularly reviewing and updating these tools to incorporate new features and functionalities. Maintains accurate records of safety inspections and audits, incidents and accidents, training sessions, and compliance activities to ensure transparency and accountability in safety practices. Supports the organization in complying with relevant federal, state, and local environmental, health, and safety regulations and standards and organization policies. Drafts limited improvement projects within a unit and introduces new supporting process activities that complement and enhance existing workflows, ensuring these activities are aligned with overall unit goals and objectives. Utilizes specialized skills to perform in-depth analysis of assigned tasks, identifying key issues and patterns and resolves moderately complex problems. u00A0 You're the right fit if you have : u200B Over 3 years of experience in industrial safety, with a strong foundation in regulated environments Advanced Diploma in Industrial Safety with specialized knowledge applicable to medical device manufacturing and operations Hands-on experience deploying ISO 45001 (Occupational Health & Safety) and ISO 14001 (Environmental Management) in compliance-driven settings Proven ability to work within multinational organizations and align safety practices with global standards and counterparts Worked with cross-functional teams including Quality, Manufacturing, R&D, and Regulatory Affairs to implement safety and environmental protocols Skilled in risk assessments, incident investigations, and driving CAPA processes to ensure product and workplace safety Strong communicator with experience delivering safety training and awareness programs across diverse teams Familiarity with global regulatory expectations including FDA, EU MDR, and ISO 13485 frameworks will be preferred Willingness to travel extensively (50% of the times) Preferred Skills: u2022 Regulatory Compliance u2022 Administrative Support u2022 Environment, Health and Safety Audit Execution u2022 Waste Management u2022 Documentation & Reporting u2022 Investigation u2022 Environment, Health and Safety Risk Management u2022 Environment, Health and Safety Knowledge How we work together We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the companyu2019s facilities. Field roles are most effectively done outside of the companyu2019s main facilities, generally at the customersu2019 or suppliersu2019 locations. This is a field role. About Philips We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others. u2022 Learn more about . u2022 Discover . u2022 Learn more about . If youu2019re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care .

The role of Transformer Bushing Quality Control and Service Professional at Hitachi Energy in Vadodara involves leading a team of young and diverse technical experts to ensure consistent quality through rigorous quality control processes for Bushings. The position focuses on addressing non-conformities and supporting continuous improvement initiatives in Testing & Services, contributing to Hitachi Energy's vision of delivering smarter and more sustainable energy solutions. As the Quality Control Engineering lead, your responsibilities include designing, developing, and implementing testing methods and equipment to ensure conformity to established quality protocols and standards. You will plan and arrange labor, schedules, and equipment required for testing, provide parameters for routine testing, specify tests to be performed, and compile data to define necessary changes to testing equipment, procedures, and processes. Additionally, you will establish and manage the bushing testing team and test lab, ensuring the availability of necessary resources for effective customer inspection of finished goods. Your role involves leading type testing activities in third-party test laboratories, responding as the first point of contact for service support, and participating in the establishment of the test laboratory. You will be responsible for building, motivating, and guiding a team of testing and services professionals to achieve organizational goals. This includes coordinating with customers, capturing Voice of Customer (VoC), Customer Complaint Resolution Process (CCRP) cases, and ensuring systematic problem-solving through root cause analysis. Furthermore, you will apply principles of business process management to create processes for consistent results and implement improvements for greater efficiency in delivering products and services. Compliance with external and internal regulations, procedures, and guidelines, as well as contributions to audits and inspections to ensure regulatory standards are met, are also part of your responsibilities. To be successful in this role, you should have a degree in Electrical or Mechanical Engineering, along with 7 to 10 years of experience in testing and type testing of bushings and transformers. Knowledge of quality management systems, regulatory requirements, industry standards (e.g., ISO, IEC), RCA, CAPA processes, and strong analytical and problem-solving skills are essential. Effective communication, interpersonal skills, and the ability to work collaboratively across teams and organizational levels are also key qualifications for this position.,

The ideal candidate for this position should hold a BSc/MSc degree in Chemistry with 2 to 4 years of relevant experience. The job is located near Vadodara and offers a salary ranging from 4.50 to 5.50 Lacs per annum. Previous experience with IKEA Suppliers is highly desirable for this role. Responsibilities include ensuring compliance with relevant chemical and regulatory standards, coordinating testing with third-party labs, and interpreting results. The successful candidate will be responsible for tracking and maintaining compliance status and documentation, supporting customer and certification body audits, and collaborating with R&D, Procurement, and Production teams. Additionally, addressing compliance risks through CAPA processes, staying updated on regulatory changes and best practices, and possessing knowledge of PDOC, GONOGO, and IKEA Connect are preferred qualifications for this position. This is a full-time job that offers Provident Fund benefits. The work location is in person.,

Looking for a qualified candidate with a passion for delivering computer system validation and risk management approaches to support significant IT and business growth. As a part of the ITRMC (IT Risk Management & Compliance) team, you will work closely with the quality business unit, IT, business customers, and vendors on various computer system validation projects and compliance initiatives. Over the next 3 years, our organization plans to deploy major operational systems like LIMS, ERP, MES, VLMS, and EBR to enhance capabilities and improve customer and patient service. Your role will be crucial in achieving these objectives. Your responsibilities will include providing technical and compliance expertise for executing computer systems validation in compliance with regulatory standards such as 21 CFR Part 11, 211, 820, GAMP, and CSA. You will conduct IT change control impact assessments, develop project documentation, and artifacts, and lead compliance improvement initiatives. Additionally, you will oversee computer system validation efforts, offer guidance on best practices, risk management, and industry trends, and provide support for IT audits by internal and external entities. To be successful in this role, you should have a Bachelor's degree in Computer Science, IT, or a science-related discipline, with at least 8 years of experience in the pharma regulated industry focusing on validation of laboratory, quality, or manufacturing IT systems. Strong knowledge of lab systems, manufacturing systems, quality systems, Document Management Systems, risk management, and audits is required. Familiarity with SDLC/GAMP, Agile cGMP development, and FDA CSA is preferred, along with Lean Six Sigma and/or ASQ certification. If you have operated as a computer systems validation strategy lead, delivered validation packages for IT systems, designed compliance processes, conducted risk management, and worked on data integrity projects in a biopharma or manufacturing environment, you are encouraged to apply. Your expertise in executing computer systems validation within an SDLC framework, collaborating with IT SMEs, and driving cultural change will be highly valued. The ideal candidate must be proficient in English and be a U.S. or UK citizen. If you are ready to take on this challenging yet rewarding role and contribute to our organization's growth and compliance objectives, we look forward to receiving your application.,