359 Quality Documentation Jobs - Page 5

As a Quality Engineer at Winfra Buildtech, you will play a crucial role in ensuring the production of premium Zincalume Storage Tanks & Grain Silo of exceptional quality. With 3 to 5 years of experience, you will be responsible for overseeing production planning and management, quality assurance, process improvement, documentation and reporting, compliance with standards, supplier quality management, training and development, and problem-solving. Your expertise in the Sheet Metal fabrication line, press shop, weld shop, plating, Customer Audit, Good Quality Control, PPAP, APQP, Quality Documentation, and Team Handling will be essential in carrying out your responsibilities effectively. You will work closely with engineering, procurement, and manufacturing teams to develop and implement production plans, quality control procedures, and process improvements. Additionally, you will be required to maintain detailed records of quality inspections, prepare quality reports, ensure compliance with industry standards, evaluate suppliers, provide training to staff, and investigate and resolve quality-related problems. Your qualifications should include a Bachelor's degree in Mechanical Engineering or a related field, along with experience in quality engineering or quality control in the metal structure or PEB industry. Certifications related to quality management such as Six Sigma, ISO 9001, or Certified Quality Engineer will be advantageous. Strong communication, problem-solving, and analytical skills are essential for this role, along with the ability to collaborate effectively with cross-functional teams and suppliers. The working conditions may involve regular site visits and occasional extended hours to meet project deadlines. If you are passionate about ensuring superior quality standards, driving process improvements, and contributing to a dynamic manufacturing environment, this role as a Quality Engineer at Winfra Buildtech is the perfect opportunity for you.,

The Senior Executive Quality position at WIKA Process Solutions India Pvt Ltd, based in Palwal, is a full-time on-site role that requires overseeing quality assurance and control processes. As the Senior Executive Quality, your primary responsibilities will include conducting compliance audits, managing quality documentation, and ensuring that all products adhere to established quality standards. Collaboration with cross-functional teams will be a key aspect of this role, as you will work towards maintaining and enhancing quality systems and processes. In addition, you will be tasked with investigating and resolving any quality issues or customer complaints, while also driving continuous improvement initiatives. The ideal candidate for this role should possess a strong background in Quality Assurance and Quality Control, along with experience in conducting compliance audits and managing quality documentation. A comprehensive understanding of quality management systems and processes is essential, as well as excellent communication and collaboration skills. Problem-solving abilities, analytical skills, attention to detail, and a dedication to continuous improvement are also key qualities we are looking for. A Bachelor's degree in Quality Management, Engineering, or a related field is required for this position. Previous experience in the manufacturing or process solutions industry would be advantageous. If you are a proactive and detail-oriented professional with a passion for maintaining quality standards and driving continuous improvement, we encourage you to apply for the Senior Executive Quality role at WIKA Process Solutions India Pvt Ltd.,

You are a highly skilled and experienced Quality Engineer with at least 3+ years of experience, seeking to join our team. Your main responsibilities will include implementing and monitoring quality control procedures throughout the fabrication process. You will be required to conduct in-process and final inspections of fabricated steel structures such as beams, channels, and plates. Additionally, you will be responsible for preparing and maintaining quality documentation, including inspection reports, NCRs, and test certificates. Collaboration with the production and engineering teams to resolve quality-related issues will be a key aspect of your role. Your previous work experience as a Quality Engineer will be beneficial in ensuring the safety and quality of our products and procedures through rigorous inspections, implementation of quality control measures, and identification of areas for improvement. As a Quality Engineer, you will work closely with cross-functional teams to address quality issues, drive continuous improvement, and contribute to building high-quality products that exceed customer expectations. The ideal candidate will have a strong background in engineering or quality assurance, exceptional attention to detail, and a proactive mindset. If you are passionate about quality and delivering excellence, we encourage you to apply and become a valued member of our team. This is a full-time position with benefits including health insurance and Provident Fund. The work location is in Jamshedpur, Jharkhand. Relocation or a reliable commute to this location is preferred.,

Job Description: QC Engineer Wiring Harness Key Responsibilities: Perform detailed inspection and quality checks of cable harness assemblies as per defined standards. Conduct First Article Inspection (FAI) on wiring harness components to ensure compliance with specifications. Manage and execute Quality Management System (QMS) audits to maintain process adherence and certification requirements. Coordinate and support Customer Pre-Dispatch Inspections (PDI) to ensure product quality before shipment. Investigate and resolve customer complaints related to wiring harness quality issues. Document inspection reports, non-conformance reports, and corrective action plans. Collaborate with production, engineering, and quality teams to implement quality improvements. Ensure adherence to safety, quality, and compliance standards throughout the inspection process. Required Skills & Knowledge: Strong knowledge of cable harness inspection techniques and standards. Experience in conducting First Article Inspection (FAI). Familiarity with Quality Management System (QMS) audits. Ability to manage customer pre-dispatch inspections and effectively communicate with customers. Problem-solving skills to handle and resolve customer complaints. Good documentation and reporting skills. Knowledge of relevant industry standards and quality processes.

Responsibilities: * Conduct quality inspections & checks * Ensure compliance with ISO standards * Maintain accurate documentation * Prepare audit documents * Collaborate on continuous improvement initiatives Provident fund

Responsibilities: * Manage quality systems implementation & documentation * Ensure compliance with ISO standards through audits & documentation * Collaborate on Capa initiatives within QMS framework Annual bonus Provident fund Mobile bill reimbursements

Overview Designation : Graduate Engineer Trainee Nature of Job : Production/ Quality / Documentation / Packing work Work location : Vallakkottai Joining immediate Salary : Rs.22000 to 25000 Food and cab facility available Interview Address : Swagatham Resource Management India Pvt Ltd No: 14 Sarathy Nagar 1st main road, Velachery, Chennai 600 042 Time : 9 am to 5pm [ All working days ] Before applying for this position you need to submit your online resume . Click the button below to continue.

Overview Designation : Graduate Engineer Trainee Nature of Job : Production/ Quality / Documentation Work location : Chennai [ Vallakkottai ] Joining immediate Salary : Rs.22000 to 25000 Food and cab facility available Interview Address : Swagatham Resource Management India Pvt Ltd No: 14 Sarathy Nagar 1st main road, Velachery, Chennai 600 042 Time : 9 am to 5pm [ All working days ] Before applying for this position you need to submit your online resume . Click the button below to continue.

Overview Designation : Graduate Engineer Trainee Nature of Job : Production/ Quality / Documentation Work location : Chennai [ Vallakkottai ] Joining immediate Salary : Rs.22000 to 25000 Food and cab facility available Interview Address : Swagatham Resource Management India Pvt Ltd No: 14 Sarathy Nagar 1st main road, Velachery, Chennai 600 042 Time : 9 am to 5pm [ All working days ] Feel free to call us for any clarification #Swapna 7845828845 Before applying for this position you need to submit your online resume . Click the button below to continue.

Examine products, materials, production processes to ensure meet required specifications & standards Record inspection results, create test reports, document Ability to use measuring tools (calipers, micrometers) read blueprints & technical drawings

As a Quality Control Tester, you will be responsible for designing and implementing testing plans to monitor products for quality and consistency. You will conduct quality improvement research, recommend new procedures, and analyze data to identify areas for enhancement. Your role will involve ensuring quality control by removing or discarding products that do not meet specifications. Regular audits and inspections will be conducted by you to guarantee compliance with quality standards. Additionally, you will maintain records of audit reports, customer-related records, and quality documentation. This is a Full-time job opportunity suitable for Freshers. The benefits include Provident Fund. The work schedule is during the Day shift. A Diploma is preferred as an educational qualification. The work location is in person.,

Understand requirement and inspection level as per EN 10204 Ensure compliance with customer requirements, product specifications, and relevant industry standards (e.g., ISO, BIS, ASME, DIN). Maintain proper records of inspection reports, non-conformities, and corrective actions. Close all punch points on Dossier and seek order clearance Review inspection pre-requisite like Approved QCP , GAD, Scope of inspection Conduct and review various NDT test like UT,PT, RT Shall have knowledge of various material like Cast Iron , Steel, Plastic, fasteners with respective grades and standards. Required Qualifications and Skills: Education - Diploma in Mechanical Engineering / BSc Experience - 5- 6 Years in customer Inspection and Documentation Skills - Strong understanding of engineering drawings, inspection standards, and quality documentation Excellent communication and interpersonal skills to interact with customers Proficiency in MS Office and familiarity with SAP & QMS systems. Ability to handle pressure and manage inspection schedules effectively. NDT L II VT, PT

Simulation experience in either ASPEN/HYSIS/UNISIM both in Dynamic and Steady Sate simulation Experience in deploying Operator Training Simulator in an operating company. Experience in plant operations. Experience in plant startup & commissioning Configuration experience working on control systems, DCS / PLC / Safety Systems. Programming skills C Sharp, Dot net, Python, VB is an added advantage. At least 5+ years of experience in Simulation for refining/petrochemical process and minimum 2 yrs exp in Plant operations Strong domain knowledge & Chemical Engineering principles and operations. Good communication, writing & presentation skills. Knowledge of DCS and ESD will be added advantage. Ability to work in a team Strong ability to maintain good working relationship with customers. At least 5+ years of experience in Simulation for refining/petrochemical process and minimum 2 yrs exp in Plant operations Strong domain knowledge & Chemical Engineering principles and operations. Good communication, writing & presentation skills. Knowledge of DCS and ESD will be added advantage. Ability to work in a team Strong ability to maintain good working relationship with customers. The role will have a broad set of responsibilities encompassing the following: Responsible for executing OTS projects with project teams for end-to-end design & delivery for Refinery, Oil & Gas, Petrochemical, and other customers Manage the development of functional and concept technical design specifications Ensures implementation is done with respect to project standards and quality documents & final deliverable meets the functional specifications of the end user Identify, advise, and incorporate modifications in simulation configuration. Should be able to anticipate the project risk and look for mitigation plan Attend project reviews with Customer & Interface with project leads and customers for rasing technical queries Strong understanding of Refinery Process and & Critical Section. Having hands on Simulation experience in modelling Distillation columns, heat exchangers, rotating equipment, Reactors, Furnaces, Turbines etc. Participation in quality process reviews. Ensure completion of projects on schedule and within the allocated budget. Drive product improvement, productivity & Self skill enhancement. The role will have a broad set of responsibilities encompassing the following: Responsible for executing OTS projects with project teams for end-to-end design & delivery for Refinery, Oil & Gas, Petrochemical, and other customers Manage the development of functional and concept technical design specifications Ensures implementation is done with respect to project standards and quality documents & final deliverable meets the functional specifications of the end user Identify, advise, and incorporate modifications in simulation configuration. Should be able to anticipate the project risk and look for mitigation plan Attend project reviews with Customer & Interface with project leads and customers for rasing technical queries Strong understanding of Refinery Process and & Critical Section. Having hands on Simulation experience in modelling Distillation columns, heat exchangers, rotating equipment, Reactors, Furnaces, Turbines etc. Participation in quality process reviews. Ensure completion of projects on schedule and within the allocated budget. Drive product improvement, productivity & Self skill enhancement.

To write, review and manage the production of high quality clinical and safety documentation for submission to regulatory authorities in support of To write, review and/or manage the production of high quality clinical and safety documentation for submission to regulatory authorities in support of marketing applications. To provide authoritative documentation-related consultancy to other line functions. To coach/mentor and/or train less experienced writers. Major accountabilities: To author, review and/or independently manage high quality clinical and safety documents: complex Clinical Study Reports (CSR), Risk Management Plans (RMP), complex CTD submission documents (clinical overviews, summaries of clinical efficacy and safety, summaries of clinical pharmacology and biopharmaceutics), other documents for health authorities (e. g. , Briefing Books, answers to questions). Lead writing team for complex submissions, actively contributing to key messaging and pooling strategy, providing expert content guidance for clinical portions of the CTD, and ensuring compliance of documentation to internal company standards and external regulatory guidelines. Ad-hoc member of Clinical Trial Team (CTT) / extended member of Safety Management Team (SMT). Core member of multiple Clinical Submission Teams (CST). Extended member of Global Clinical Teams (GCT). Input into planning of data analyses and presentation (statistical analysis plan review and meetings) used in CSRs, submission documents and/or answers to questions. Documentation expert in GCTs and CSTs to ensure compliance to internal company standards and external regulatory guidelines. Provide content and strategic expertise for clinical portions of the CTD. Program Writer for large and/or complex programs ensuring adequate medical writing resources are available for assigned program and consistency between documents. Lead process improvement in RWS and cross-functional initiatives and/or activities. Can identify training needs to foster high level of performance within RWS. Coach and/or mentor less experienced writers. Leader in cross-functional communication to optimize feedback and input towards high quality documents. Maintain audit, SOP and training compliance. Key performance indicators: Delivery of high quality clinical and safety documents in time and in compliance with internal and external standards, according to RWS metrics. Completion of an adequate volume of work (taking into account complexity) per year in accordance with the Key Performance Indicators. Work Experience: 6 years medical writing experience or other relevant pharma industry experience combined with scientific and regulatory knowledge, plus expert knowledge of medical writing processes. Expert knowledge of and repeat experience in global regulatory environment and process (key regulatory bodies, key documents, approval processes, safety reporting requirements). Expert knowledge, extensive experience, and demonstrated record of accomplishment in global registering of drugs. Excellent communication skills (written, verbal, presentations) Expert knowledge of biostatistics principles. Proven ability to prioritize and manage multiple demands and projects. Demonstrated ability to define and solve complex problems ( Problem-solver ) Broad knowledge and future oriented perspective Proven ability to drive and manage organizational and team performance across cultures. Proven track record in matrix environment Repeat experience in managing global, cross-functional teams or complex global projects. Demonstrated ability to motivate and coach people.

Gigamon is seeking a self-motivated individual to join the Technical Publications team in providing customer documentation for its highly acclaimed Visibility product portfolio. The individual will work closely with Product Managers, Development Engineers, QA and Solutions Engineers to develop and deliver customer documentation. As part of a dynamic cross-functional team, the candidate will thrive in helping to improve the customer experience by delivering high-quality documentation for Gigamon products. What You ll Do: Develop customer documentation for Hardware and Software, CLI and GUI-based documentation. Follow documentation standards and best practices. Participate in Engineering specification reviews. Provide documentation on time and in line with product release dates. What You ve Done: Minimum 6+ years of experience in technical writing. Self-starter who can multi-task, seek out information on assigned tasks in a fast-paced, collaborative team environment. Proficiency with PC Desktop tools. Exposure to MadCap Flare, Madcap Central, Adobe Acrobat, Confluence Exposure to XML documentation, HTML5, and CSS. Who You Are: Technical background in networking and/or network security products.\ Passion for producing customer-facing instructional content that is accurate, concise, and easy to understand.

Position: Engineer Department: Quality Assurance Position Summary: Adroit USA, an US based collaborator in developing and manufacturing class II & III medical devices is seeking a qualified and detail-oriented QA Engineer for its Bommasandra/Peenya, Bengaluru location. Join an organization with a passion for commercializing smart, effective and patient centric medical device solutions. The Engineer is a key member of the site Leadership Team and this role leads the AUSAMD in Bengaluru, supervise the activities of a team of Quality . Job Description: To be able to understand work instructions and perform Basic knowledge in APQP, PDCA, control plan SAP QM SPC 7QC tools. Coordinate with other functions to ensure smooth process of QMS/protocols. Coordinate with other functions to ensure smooth process of QMS/protocols. Visual inspection of final parts after machining and after plating Having knowledge of in process activities Having knowledge of 1st off inspection activities Document control to ensure correct revision levels Monitoring final inspection as per control plan, as per documentation of project Understand the drawings and make sure that all specified points or dimensions are properly inspected to prepare a document. Knowledge of using VMS, Vernier calliper, micrometre, height gauge, slip gauges, plunger dial gauges Profile projector etc. Knowledge in GD&T. Working on ISO 13485 documentations and filings. Inhouse inspection, rejection and rework report, and handling supplier quality issues & in house complaint. Knowledge, And Skills Knowledge in GD&T. Working on ISO 13485 documentations and filings. knowledge in APQP, PDCA, control plan SAP QM SPC 7QC tools. Keywords To be able to understand work instructions and perform. To be able to read write of protocols and the function and follow ups. Good Communication skills Computer Knowledge. Qualification / Experience Diploma in Mechanical Engineering (DME) with 03 Years & Bachelor of Engineering in Mechanical (BE) 2+ years of experience. Job Function: (Incoming & calibration) Industry: AUSA Medical Devices Private Limited What's on Offer: Attractive salary package and Friendly environment, Canteen Facility & Medical Insurance. 1 of 2

TrioVision is looking to fill following roles: LOOKING FOR IMMEDIATE JOINERS QUALITY ENGINEER-05 ,QMS ENGINEER-02 Diploma/BE/BTech/ME/MTech Mechanical/Industrial/Production engineering with 1-5 years experience in manufacturing industry. Composites experience preferred. PLANT WORK LOCATION: KADAPA-ANDHRAPRADESH. Mail id: careers@triovisioninternational.com contact no:8919993254 NOTE: This is onsite job, candidate has to move to Kadapa, and work here for minimum 2 years, all interviews takes place in Kadapa, in face to face manner only. Job Description Quality Management Internal and External Audits Quality Control & Quality Assurance Receiving Inspection and Materials Participate in QA process, developed include Flow Charts and Control Plans. Develop the required documentation for each specific customer requirements. Maintain customer contacts by being proactive and reactive to all customer concerns for internal and external customers. Perform capability studies as required. Participated in internal auditing and layered audits. Developed, implemented, and provided training. Participate on multiple Project Teams as a Quality Engineering Representative, ensuring compliance to regulatory standards and providing input into the project design input requirements and product development quality plans. Proficient in application of Design Controls, Good Manufacturing Practices and ISO. Developed and validated various test methods. Established In-process Production and Final QA Inspections plans. Provided technical guidance to Quality Technicians and Inspectors. Utilized statistical methods, such as, process capability data analysis, statistical process control (SPC), and scientific sample size selection to ensure processes capability and repeatability and to determine statistically valid sampling plans. Provided technical support to solve quality problems in product development and manufacturing. Performed Design of Experiments to support process optimization. Participated and conducted the design transfer and design review aspects of design control for QE input / support. Conducted Internal Audits per Internal SOP, QSR Regulations, and ISO requirements. Analyzes data by completing hypothesis, normal distribution, and process capability analysis tests. Prepares reports by collecting, analyzing, and summarizing data; making recommendations. Internal Regularly interact with Materials, Quality, Engineering, Sales, and all Manufacturing functions. External Regularly interact with all levels of customers and prospects. Offers exemplary customer service, including maintaining customer relationships and ensuring repeat customers by up-selling products and services and taking care of any customer concerns or complaints quickly and professionally. Industry MECHANICAL-COMPOSITE MANUFACTURING INDUSTRY

Manage the Quality Assurance function at manufacturing site Ensure compliance with ISO, GMP & REACH standard Develop, implement & monitor Quality Management Systems including SOPs, documentation & CAPA systems Handle customer complaints, conduct RCA Required Candidate profile 10-12 years of experience in QA, preferably in specialty chemicals Knowledge of analytical instruments, QC processes & technical documentation Strong knowledge -ISO 9001, GMP & other quality standards

Our world is transforming, and PTC is leading the way. Our software brings the physical and digital worlds together, enabling companies to improve operations, create better products, and empower people in all aspects of their business. Our people make all the difference in our success. Today, we are a global team of nearly 7,000 and our main objective is to create opportunities for our team members to explore, learn, and grow all while seeing their ideas come to life and celebrating the differences that make us who we are and the work we do possible. Job Overview: As a Senior Technical Writer, you will be responsible for working independently on information development projects. You will collaborate with cross-functional teams to produce high-quality content and contribute to larger team on projects as needed. Required Skills: 2+ years of experience in writing about enterprise software, ERP systems, or similar applications Working knowledge of any CRM application like Salesforce.com, Siebel, PeopleSoft, or Oracle Demonstrate track record in delivering innovative and high-quality documentation and working based on broad objectives and with minimal handholding Ability to collaborate with subject matter experts to research software products, understand requirements, determine functionality and design features, and communicate effectively to the user Skilled in core information development processes: content planning, content creation, content review Excellent communication skills and impeccable attention to detail Strong writing and editing skills. Strong technical skills, with the ability and enthusiasm to quickly learn how the system works. Skilled in time management, able to meet tight deadlines with multiple deliverables Knowledge of core technical communication concepts, topic-based authoring, minimalism and task-oriented design Senior-level experience with structured authoring and developing modular content for single-sourcing and reuse. Experience using various style guides, such as the Microsoft Manual of Style Experience in writing content using authoring tools such as Arbortext Editor Exposure to SaaS/Cloud-based business applications Job Responsibilities: Produce high-quality documentation that is appropriate for its intended audience. Work with internal teams and cross-functional teams on documentation requirements. Keep up with the rapid changes in products and constantly strive to improve the documentation. Ability to quickly grasp complex technical concepts and make them easily understandable Analyse existing and potential content, focusing on reuse and sing-sourcing opportunities Responsible for working independently on projects Develop release notes, user guides, and administrator guides for all product lines, with cohesive content and great formatting visuals. Write clear, concise, and complete step-by- step procedures for technical products and solutions Create architecture, flow, and process diagrams to increase the visual/graphical content to complement/substitute textual content where applicable Write the content in the authoring tools like Arbor text Editor as per the existing style guides and procedures Guide and work with other technical writers in the team for scoping, assigning and managing tasks to ensure their timely completion Provide technical, structural, and infrastructural strategy for the team Meet all deadlines, while maintaining high quality and standard of the deliverable. Nice-to- have Skills/Experience: Working knowledge of Arbor text Editor Exposure to Agile development methodologies Life at PTC is about more than working with today s most cutting-edge technologies to transform the physical world. It s about showing up as you are and working alongside some of today s most talented industry leaders to transform the world around you. If you share our passion for problem-solving through innovation, you ll likely become just as passionate about the PTC experience as we are. Are you ready to explore your next career move with us? We respect the privacy rights of individuals and are committed to handling Personal Information responsibly and in accordance with all applicable privacy and data protection laws. Review our Privacy Policy here ."

Our world is transforming, and PTC is leading the way. Our software brings the physical and digital worlds together, enabling companies to improve operations, create better products, and empower people in all aspects of their business. Our people make all the difference in our success. Today, we are a global team of nearly 7,000 and our main objective is to create opportunities for our team members to explore, learn, and grow all while seeing their ideas come to life and celebrating the differences that make us who we are and the work we do possible. Job Overview: As a Senior Technical Writer, you will be responsible for working independently on information development projects. You will collaborate with cross-functional teams to produce high-quality content and contribute to larger team on projects as needed. Required Skills: 2+ years of experience in writing about enterprise software, ERP systems, or similar applications Working knowledge of any CRM application like Salesforce.com, Siebel, PeopleSoft, or Oracle Demonstrate track record in delivering innovative and high-quality documentation and working based on broad objectives and with minimal handholding Ability to collaborate with subject matter experts to research software products, understand requirements, determine functionality and design features, and communicate effectively to the user Skilled in core information development processes: content planning, content creation, content review Excellent communication skills and impeccable attention to detail Strong writing and editing skills. Strong technical skills, with the ability and enthusiasm to quickly learn how the system works. Skilled in time management, able to meet tight deadlines with multiple deliverables Knowledge of core technical communication concepts, topic-based authoring, minimalism and task-oriented design Senior-level experience with structured authoring and developing modular content for single-sourcing and reuse. Experience using various style guides, such as the Microsoft Manual of Style Experience in writing content using authoring tools such as Arbortext Editor Exposure to SaaS/Cloud-based business applications Job Responsibilities: Produce high-quality documentation that is appropriate for its intended audience. Work with internal teams and cross-functional teams on documentation requirements. Keep up with the rapid changes in products and constantly strive to improve the documentation. Ability to quickly grasp complex technical concepts and make them easily understandable Analyse existing and potential content, focusing on reuse and sing-sourcing opportunities Responsible for working independently on projects Develop release notes, user guides, and administrator guides for all product lines, with cohesive content and great formatting visuals. Write clear, concise, and complete step-by- step procedures for technical products and solutions Create architecture, flow, and process diagrams to increase the visual/graphical content to complement/substitute textual content where applicable Write the content in the authoring tools like Arbor text Editor as per the existing style guides and procedures Guide and work with other technical writers in the team for scoping, assigning and managing tasks to ensure their timely completion Provide technical, structural, and infrastructural strategy for the team Meet all deadlines, while maintaining high quality and standard of the deliverable. Nice-to- have Skills/Experience: Working knowledge of Arbor text Editor Exposure to Agile development methodologies ?

Detailed job description - Skill Set: Technically strong hands-on Self-driven Good client communication skills Able to work independently and good team player Flexible to work in PST hour(overlap for some hours) Past development experience for Cisco client is preferred.

Develop and implement quality control procedures and processesConduct quality audits and inspections of products and processesIdentify and report quality issues and work with production and engineering teams to resolve themDevelop and analyze statistical data and product specifications to determine quality standards and to monitor process capabilitiesDevelop and maintain quality documentation and recordsEnsure compliance with relevant quality standards and regulationsParticipate in product and process design reviews to ensure quality requirements are metStrong understanding of quality control principles and practicesExperience with quality tools and methodologies such as Six Sigma and Lean ManufacturingExcellent communication and interpersonal skills

We are hiring QMS Engineer

Regulatory Affairs Associate I Job Details | Teva Pharmaceuticals Find a Career With Purpose at Teva Search by Postal Code Area of Interest Select how often (in days) to receive an alert: Select how often (in days) to receive an alert: Regulatory Affairs Associate I Jul 9, 2025 Navi Mumbai, India, 400706 Who we are The opportunity To organize and perform required regulatory tasks in order to maintain existing EU procedures in line with current regulations, guidelines and in-house standard To obtain regulatory approvals for defined European procedures, ensuring high quality data and standards are used in all regulatory application To ensure high quality documents and standards are used in preparation of all regulatory applications to achieve rapid and successful assessment. To give regulatory support to project teams, stakeholders and other sites, as require How you ll spend your day Prepare, compile, review and submit high quality submissions for all required post-approval activities in accordance with EU legislation and in-house standards. Responsibility for MA compliance with both legislation and business needs. Prioritise, plan and monitor submissions for allocated procedures while documenting and informing involved parties of progress. Ensure approvals are secured within the stipulated timelines for designated projects. Maintain registration documentation and associated electronic databases, in line with in-house procedures. Provide regulatory support and product information for all internal and external customers, stakeholders and TEVA project teams. Communicate with other Teva departments across Europe and European Agencies regarding proposed and pending submissions. Maintain and develop awareness of current/pending regulatory legislation and guidelines. Fulfilling other allocated department duties and ad-hoc needs at the direction of Senior Regulatory Affairs personnel. Awareness of regulatory legislation and guidelines Your experience and qualifications Qualification: Required Degree: Master in Pharmacy or Master in science/life sciences Experience: Total years of experience required for the role: 2 to 3 years in Post approval Regulatory affairs Overall Pharma industry experience: 2 to 3 years Desirable to have EU experience and knowledge of European regulatory procedures. Reports To Group Leader Regulatory Affairs Teva s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Tevas global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Job Title: Quality Assurance Executive Location: Bhiwandi Company: Vistaprint India Reports to: Quality Manager Job Summary: Responsible for implementing and maintaining quality systems on the shop floor, ensuring FOA/CTQ processes, conducting inspections, managing a team of quality inspectors, and driving continuous improvement. Will handle in-process/customer complaints, perform root cause analysis, and ensure compliance with QMS, SOPs, and ISO standards. Key Requirements: 48 years of QA experience in a printing/manufacturing setup Knowledge of FOA, CTQ, QMS, ISO, 5S, RCA, and quality tools Strong team management & documentation skills Diploma/Degree in Mechanical or Printing Technology Flexible to work in shifts Facilities: Bus & Canteen provided