936 Quality Systems Jobs - Page 3

With HOD and reliever discuss: - Special requirement/ instruction/target, last 2 shift issues, another 3 shifts schedule and additional task if any. Take quick round with the reliever in the entire area: - During round try to touch each and every people and have some specific question may be which are most critical to last 2 shifts issues/area etc. Charge will be taken during round physically area: - Any abnormality observed need to be objected; also, information should go to HOD. Abnormality should be cleared by the doer before leaving the workplace. Come to planning board well advanced (before shift start) and see the schedule status on the board updated and people reporting in the shift o...

Key Responsibilities - Monitor and ensure compliance with quality standards during all stages of solar module production (cell sorting, stringing, lamination, assembly, and final testing). - Conduct in-process and final inspections, audits, and testing of PV modules as per IEC/UL standards. - Perform root cause analysis and corrective & preventive actions (CAPA) for quality issues and customer complaints. - Collaborate with production, maintenance, and R&D teams to improve process capability and product quality. - Support implementation of ISO 9001, ISO 14001, and ISO 45001 management systems within the plant. - Ensure adherence to reliability testing protocols (EL testing, IV curve measurem...

We have a requirement for Hardware Senior Engineer (HW_GCS_2) position having its own in-house Product Development Centre into design, develop, engineer, and manufacture indigenous unmanned aerial vehicles (UAVs) As a Mechatronics or Electronics engineer, you will be crucial in developing and implementing electro-mechanical systems for avionics and other electronic systems in our aerospace projects.You will work closely with cross-functional teams to ensure the successful integration of electronic components with mechanical systems into our UAS.This role offers a unique opportunity to work on challenging projects at the forefront of aerospace technology. Key Responsibilities: You will be res...

Job Title: Manager-2 - FR &D Non-Orals (Compliance group) Business Unit: R&D1 Regulatory Affairs Job Grade G11A Location : Baroda At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you ll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other s journeys. Job Description Review documents required for ...

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Key responsibilities: Engineering & Design: Evaluate customers engineering and process requirements across mechanical, instrumentation, electrical, and food engineering domains. Lead engineering and design process based on customer specifications, with full accountability for technical validation & approvals from customers. Quality & Efficiency Focus: Be fully accountable for delivery of quality, to the satisfaction of customers, in terms of equipment performance, precision, efficiency, safety & life cycle management. Implement robust quality systems, policies and performance metrics. Vendor Development & Negotiation: Develop competitive vendors across mechanical, instrumentation, electrical...

Knowledge : - Demonstrates in-depth knowledge of QA principles, concepts, industry practices, and standards. - Demonstrates a keen understanding of international quality systems regulations to adopt best-in-class systems/processes.

Relocation candidates apply* *Your one share can give Job who need it* *Position: Sr. Officer QMS* *Industry - Rubber/ Automotive* *Location Nashik Ambad MIDC* Email - jobpune2025@gmail.com *Experience* -03-08 yrs *Contact -9356395439* *Department* : Quality Assurance *Key Responsibilities* Conduct process audits, product audits, and internal audits as per the audit plan. Perform self-assessment audits and share findings with customers. Assist QMS Manager during customer audits and 3rd party certification audits. Support CSR compliance and ESG data collection & reporting. Ensure effective document control and record management in line with QMS requirements. Monitor implementation of correcti...

KEY RESPONSIBILITIES a) Dealership profitability 1. Planning and monitoring the achievement of the service targets in the area 2. Execution of primary service network (dealer workshops & branches) and secondary service network (Certified Service Technicians and Power Technicians) expansion activities 3. Identification of service gaps and recommend new dealer workshops/branches 4. Promoting the sales of Bajaj Genuine Spares and Bajaj Genuine Oil 5. Promoting referral sales by providing service support 6. Handholding of dealers for achievement of customer retention targets and overall dealership profitability b) Capability building 1. Providing guidance to dealers in the region with respect to...

We are looking for Senior Software Engineer who should be passionate about software development and technology, have demonstrable technical and problem-solving skills. We would love to speak with you if you have professional working experience in Java (Spring) and are motivated to master popular cloud technologies (AWS). About You - experience, education, skills, and accomplishments Bachelor s degree in Computer Science, Engineering, or a related field (preferred) or equivalent professional experience At least 3+ years of experience in developing software using Java At least 3+ years of experience using Spring framework At least 3+ years of experience in relational databases, ideally Oracle ...

As the Senior Director, Site Quality Head at Teva Pharmaceuticals in Goa, India, your primary responsibility will be to provide Quality oversight for Manufacturing, Packaging, and Laboratory Operations. Your key responsibilities will include: - Leading the Quality organization on site, encompassing Quality Control, Microbiology, Quality Compliance, Quality Systems, and Quality Assurance Operations. - Ensuring the implementation and continuous improvement of a current Quality Management System. - Ensuring products are manufactured, released, and distributed in accordance with cGMP requirements and registered specifications. - Assessing and mitigating risks by identifying quality risks, defini...

Vacancy for QMS Engineer in Sheet Metal Industry Exp - 3 to 5 years IATF 16949:2016, Internal Auditing, QMS, MR Responsibilities IATF/EHS Qualification - BE / Diploma Mechanical Location - Chakan Pune. On Roll Job Call on - 8408824722/ 9518340393

About Us Scimplify is a specialty chemicals manufacturing company offering a full-stack solution from R&D and custom synthesis to large-scale manufacturing and doorstep delivery. Headquartered in Bengaluru, India, we serve multiple industries ranging from pharmaceuticals to agrochemicals and industrial chemicals to personal care and fragrances. We enable 500+ businesses across 20+ countries to develop and scale innovative chemicals from lab to commercial production. We have raised over $54 million from top tier investors such as Accel and Bertelsmann, We are a team of 250+ professionals with entities in India, Japan, USA, UAE, and Indonesia. Learn more about why Forbes thinks we are the top ...

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology The Application Systems Engineer (Manufacturing Systems / Physical Security System) is responsible for perform systems administrative functions for digital tools used in our manufacturing sites, physical security and facilities systems. This position reports to the Director Portfolio Management and is part of the Manufacturing Site Ops & Sourcing located in India and will be onsite. and will be an on-site role . At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. What you will do: Application operations and maintenance activities including...

Handle customer complaints related to plastic components and ensure timely resolution. Conduct root cause analysis (RCA) using problem-solving tools (8D, Why-Why, Ishikawa, etc.). Implement corrective and preventive actions (CAPA) to eliminate recurring issues. Liaise directly with OEMs / Tier-1 customers for complaint handling and resolution updates. Lead the customer audit process and ensure compliance with quality standards. Monitor quality performance trends and prepare MIS/reports for management. Support NPD teams in validation, PPAP, and customer-specific requirements. Drive continuous improvement and cost reduction initiatives in line with quality standards. Ensure adherence to ISO/TS...

This role is responsible for client projects by route designing and synthesis of molecules as per client specifications, independently or through supervision of a team of chemist. Responsibilities Set-up and execute reactions for synthesis of target molecules Understand the project requirements and deliverables from manager as specified by the client Understand the reaction protocol and search literature as required Efficiently delegate work and monitor team members for effective planning, execution and delivery Understand and discuss the MSDS (Material Safety Data Sheet) with team members Identify and mitigate any potential safety risk with the help of supervisor Plan and execute reactions ...

This role is responsible for executing chemicals reactions to synthesize required quantities of molecules / compounds as per client specifications using efficient route and techniques. Responsibilities Set-up and execute reactions for synthesis of target molecules/ compounds: Understand the project requirements as specified by the client, the synthetic route Understand and discuss the MSDS (Material Safety Data Sheet) with team members Identify and mitigate any potential safety risk with the help of supervisor Plan and execute reactions with proper reagents and equipment (glassware, stirrers, vacuum pumps etc.) maintaining specified conditions (temperature, pressure etc.), with optimum usage...

This role is responsible for executing chemicals reactions to synthesize required quantities of molecules / compounds as per client specifications using efficient route and techniques. Responsibilities Set-up and execute reactions for synthesis of target molecules/ compounds: Understand the project requirements as specified by the client, the synthetic route Understand and discuss the MSDS (Material Safety Data Sheet) with team members Identify and mitigate any potential safety risk with the help of supervisor Plan and execute reactions with proper reagents and equipment (glassware, stirrers, vacuum pumps etc.) maintaining specified conditions (temperature, pressure etc.), with optimum usage...

ApoPharma, a member of the Apotex group of companies, is a pharmaceutical company devoted to the discovery, development and provision of new medicines to help improve the quality of life of patients with debilitating and life-threatening diseases. Investigation into the pathological role of iron in human disease, and how to use novel medicines to treat conditions created or worsened by iron, is a major research focus of ApoPharma. Job Summary Perform and report of analysis of Stability, Inprocess and Finished products, Cleaning Method validation analysis by using various analytical instruments. Job Responsibilities Analysis of Stability, Inprocess and Finished products samples, Cleaning Meth...

Post - Asst. Manager QMS Skills -+ QMS , IATF , ISO , Rubber hose , tube Email jobpune22@gmail.com Experience - 8-10 years Education - BE/ B-tech/ DME Contact - 9356395439

Focus on ISO COORDINATION, QMS IMPLEMENTATION, QUALITY MANUALS, PLANT INTERNAL AUDIT SYSTEM, conduct QUALITY SYSTEM AUDITS, QMS TRAINING, INTERNAL QMS AUDIT, DOCUMENT CONTROL, EXTERNAL AUDIT COORDINATION, MR ACTIVITY, Plan SOPs, QA CERTIFICATIONS etc Required Candidate profile BE 2+yrs exp with AUTO / ENGG Unit into QA with strong exp in SYSTEM QUALITY / QMS Must have proven exposure in ISO, TS, AITF etc Exposure in INTERNAL & EXTERNAL AUDIT, ISO COORDINATION etc must Perks and benefits Excellent Perks. Call Mr. Prabhu @ 7010863499 now

Roles and Responsibilities : Conduct internal audits to ensure compliance with quality standards and regulations. Develop and implement quality systems, processes, and procedures for automobile components manufacturing. Lead supplier audits to assess their quality management systems and identify areas for improvement. Analyze data from inspections and testing results to identify trends and root causes of defects. Job Requirements : 14-20 years of experience in the auto components industry or related field. Strong knowledge of quality documentation, inspection, compliance, root cause analysis, and supplier quality assurance. Proven track record in implementing effective quality control measur...

As a Diploma holder in Mechanical or Production, you will be responsible for managing a team of 10-12 workmen in the weld body shop. Your main focus will be on process improvement to enhance quality, productivity, and safety. You will have administrative control over the team, including manpower management, training, and skill upgradation. Achieving production and quality targets, as well as implementing loss recovery strategies, will be key aspects of your role. You should have hands-on experience in line operations, part loading sequence, and line data management. Efficiency analysis and continuous improvement through practices like KAIZEN will be essential. Training new workmen, conductin...

About Us Scimplify is a specialty chemicals manufacturing company offering a full-stack solutionfrom R&D and custom synthesis to large-scale manufacturing and doorstep delivery. Headquartered in Bengaluru, India, we serve multiple industries ranging from pharmaceuticals to agrochemicals and industrial chemicals to personal care and fragrances. We enable 500+ businesses across 20+ countries to develop and scale innovative chemicals from lab to commercial production. We have raised over $54 million from top tier investors such as Accel and Bertelsmann, We are a team of 250+ professionals with entities in India, Japan, USA, UAE, and Indonesia. Learn more about why Forbes thinks we are the top 1...

Quality Manager for Wiring Harness & Cable Assembl QMS Work with the Cross functional team to put together a Quality Management System encompassing the lifecycle of NPD projects comprising of initiation, planning, execution, control and close-out. Required Candidate profile 14+ years of experience in implementing ISO 9001,14001,IATF ISO 13485 in Manufacturing sector implementing Quality tools like Process capability MSA SPC FMEA PPAP APQP review quality performance KPIs