1357 Quality Systems Jobs - Page 9

Responsibilities: Documentation & Record Review: Review specifications, sampling instructions, test methods, and analytical reports. Review and approval of Batch Manufacturing Record (BMR), Batch Packing Record (BPR), Master Formula Record (MFR), and Equipment Qualification Records. Review completed Batch Production Records and Laboratory Control Records post-batch completion. Review analytical data, Calibration & Preventive Maintenance schedules, and external audit reports. Review and finalize Certificate of Analysis (CoA) for finished products. Review Draft Equipment Cleaning Records and Hold Time Study protocols/reports. Review Standard Operating Procedures (SOPs) and Annual Product Quali...

Lead and manage testing operations in a NABL-accredited electrical testing laboratory. Supervise and guide all engineers to ensure efficient team performance. Maintain full compliance with NABL & ISO 17025 standards and laboratory procedures. Review. Required Candidate profile High Voltage (HV) Test Sets Insulation Resistance Testers (Megger) Earth Resistance and Earth Leakage Testers Transformer Testing Equipment, ower Analyzer, Multimeters, and Clamp Meterr

Job Description Summary Chemical Process Quality Engineer with the responsibility to provide special process and chemical process support in the Asian region. Drive quality across Chemical Process supply chain, including quality plan implementation. Support suppliers through qualification processes. Own supplier results, drive improvements utilizing supplier scorecards. Own supplier audits, ensuring compliance, and driving improvement plans where needed. In-depth understanding of key business drivers; uses this understanding to accomplish own work. In-depth understanding of how work of own team integrates with other teams and contributes to the business. Has experience and expertise to solve...

As a Child Part Development Engineer, your role involves timely development and localization of child parts. You will closely work with the New Model Development (NMD) and Quality Assurance (QA) departments. Your responsibilities will include: - Developing all child parts (plastic, sheet metal, rubber, injection moulding) for new projects according to the specified requirements. - Evaluating suppliers" competency, conducting SWOT analysis, and ensuring alignment with child part requirements to expand the Approved Vendor List. - Ensuring that the parts meet customer specifications and requirements, and submitting samples as per customer milestones. - Conducting first principle costing of chil...

Zeno is seeking a Supply Chain Manager Frame & Structural to lead the sourcing, procurement, and vendor development of critical structural components, including chassis, frames, and other load-bearing elements of our electric two-wheelers. Location: Bengaluru Work from Office (5 days a week) Start Date: Immediate About Zeno An unprecedented energy transition has begun. To meet 2040 net zero goals, over 2 billion electric two-wheelers (motorcycles) must be sold and $11 trillion in fuel consumption replaced. Zeno is building a tech platform to electrify this two-wheeler market, currently responsible for more than 4% of the world's GHG emissions. Our mission is to accelerate the energy transiti...

As a Design Engineer - Solar (Civil/Structural) at EDRC - (Solar), your role involves complete design and detailed engineering of Civil Structural Engineering for PV Solar Power plants. You will be responsible for managing the engineering activities within budget, delivering on time, and maintaining a high quality of engineering. Your key responsibilities will include: - Timely review of the drawings developed by the draftsman - Detail design of Civil and Structural components of Solar Plants such as Module mounting Steel Structures, Buildings, Road, Drain, Fence/Compound Wall, Grading, and leveling cable Trenches - Preparation and review of Pre-bid queries, DBR, BOQ & Scope of work for Prop...

Role Overview: As a Quality Assurance SPOC at VOIS India, your role is crucial in ensuring the transaction quality of activities performed by the HR operations team for data integrity and accuracy. Your primary objective will be to achieve quality assurance operational objectives by contributing information and analysis for strategic plans and reviews. You will be responsible for preparing and completing action plans, implementing productivity, quality, and customer-service standards, identifying and resolving problems, completing audits, determining system improvements, and implementing changes. Key Responsibilities: - Responsible for HR Ops Quality Audits - Prepare Monthly Quality Dashboar...

Department: R&D Quality (GPvP QA) Designation: Executive (QA Pharmacovigilance) Location: Gurgaon Job Description (jd) Assist in developing global Pharmacovigilance system auditing program and responsible for conducting and reporting audits being a lead auditor/co-auditor for outsourced parties (CROs, Service Providers, Vendors), Affiliates & Partners etc., associated with Sun Pharma Pharmacovigilance operations. Assist in conducting and reporting audits for Sun Pharma sites associate with Pharmacovigilance activities/ operations to assure adequacy & adherence with established Quality Systems. Management of Internal Audit Observation Database (IAOD) with the perspective of sharing audit repo...

Active involvement in all upstream manufacturing activities. Perform error free operation by eliminating operational gaps in advance. Active trouble shooting to minimize the various risks prior to execution and during execution. Initiate and process upstream deviations /investigations and closure. Pre -execution activity: Area and equipment readiness. Issuance of raw material /consumables and issuance batch records. Upstream process execution: Batch process operation /unit operation (including CIP, SIP and preparation upstream accessories), close monitoring of batch performance and data. Follow and practice on-line documentation all the time. Follow cGMP practices during the manufacturing ac...

Management and control of SOPs, Master documents, labels & other GMP impacted documents Implementing necessary quality systems at the site including complaint Investigation, qualification and validation, change control, deviation and non-compliance management, documentation, supplier quality assurance etc Out of specification & Out of trend investigation Deviation Investigation Incidence investigation Review of Batch Manufacturing Records (BMRs), Analytical record & related documentation Validation & Qualification Change control review & management Preparing the Annual Product Review and Annual Quality Review Batch Rework/Reprocessing Approval Approval of repacking, relabeling and non-standa...

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 and minimum wastage Ensure parallel execution of multiple reactions Monitor the reaction by observing progress by using analytical techniques Identify and execute appropriate workup and purification technique to produce an intermediary / final compound of desired quality Anal...

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 and minimum wastage Ensure parallel execution of multiple reactions Monitor the reaction by observing progress by using analytical techniques Identify and execute appropriate workup and purification technique to produce an intermediary / final compound of desired quality Anal...

Responsibilities: * Lead quality initiatives * Ensure compliance with ISO standards * Oversee internal audits & inspections * Implement QMS strategies * Develop & maintain quality policies & procedures Food allowance Health insurance Annual bonus Provident fund

As a Civil and Structural Engineer at our company, your main responsibility will be to execute civil and structural works to support plant operations. This includes implementing effective department working standards and procedures to ensure compliance with the organization's quality systems requirements. You will also be in charge of guiding a team of contract engineers and handling spares planning and procurement. To apply for this position, please share your resume with mv41@sanmargroup.com and ns52@sanmargroup.com.,

Job Description: You will be responsible for supporting the development, assembly, and optimization of the innovative Auskey Digital Stethoscope. Your role will involve research and development, process setup, quality systems, and technical documentation in a fast-paced med-tech environment. Key Responsibilities: - Support the development of the Auskey Digital Stethoscope - Handle the assembly and optimization processes - Establish and maintain quality systems - Prepare technical documentation related to the product Qualifications Required: - Bachelor's degree in a relevant field - Experience in research and development within the medical technology industry - Strong understanding of quality...

As a Production Technology and Maintenance Specialist at our company located in IND Rewari - Bawal, you will play a crucial role in ensuring compliance with quality systems, policies, procedures, and safety regulations. Your primary responsibilities will involve investigating and resolving loss issues, developing maintenance standards, coaching technicians and operators, and executing maintenance activities in the line. Key Responsibilities: - Investigate and resolve Loss issues (Breakdown, Waste, Speed) by attending meetings and providing engineering status updates. - Resolve repeat loss issues using systematic problem-solving techniques. - Support Shift Technicians in investigating losses ...

As a Senior Manager in the Powertrain Production (Machine Shop) department at Ahmedabad Plant, your main responsibility will be overseeing the Powertrain Cylinder Block Machining operations. You will be reporting to the DGM of Powertrain Cylinder Block & Head Machining and will be responsible for resolving process and quality issues related to engine assembly and testing. Your role will also involve identifying engine defects, leading root cause analysis, setting up new model machining processes, implementing capacity improvements, and driving revenue cost reduction initiatives. Additionally, you will be expected to generate improvement ideas, develop safety working culture, and implement TP...

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...

Job Purpose To ensure the Shift activities on quality parameters are working in good condition and maintaining BIS records. Job Context & Major Challenges UltraTech Cement Limited has an annual capacity of 116.75 million tonnes. It manufactures and markets Ordinary Portland Cement, Portland Slag Cement and Portland Pozzalana Cement. It also manufactures ready mix concrete RMC. The Company has 23 integrated plants, 26 grinding units, 7 bulk terminals including one in Sri Lanka and 5 captive jetties which includes significant presence in the Middle East with 2 grinding units and 1 clinkerisation plant in UAE, and 1 grinding unit in Bahrain. UltraTech Cement is the country largest exporter of c...

About Us Zapcom is a global Product Engineering and Technology Services company, specializing in bespoke, customer-centric solutions across industries like BFSI, e-commerce, retail, travel, transportation, and hospitality. Headquartered in the US, with a presence in India, Europe, Canada, and MENA, we excel in transforming ideas into tangible outcomes using AI, ML, Cloud solutions, and full-stack development. At Zapcom, we value accountability, ownership, and equality, empowering you to excel. We listen to your aspirations and provide the support needed to achieve them. Our diverse, collaborative culture ensures every voice is heard, driving innovation and business value. With global opportu...

Position Overview The Quality Head is the senior quality leader responsible and accountable for the overall Pune site Quality organization and contractors under the Quality Shared Services remit You will be the executive quality representative responsible for maintaining strict compliance with corporate, divisional, and regulatory quality system standards throughout the Pune Site, Global Quality Shared Services (GQSS), and associated and approved contractors This role reports to the AVP, Global Quality Management Systems, and is a member of the Global QMS Leadership team This role has significant and impactful responsibility, including executive quality leadership and decision making, regula...

Your primary role is to be a vital member of the team and a main point of contact for customer projects Your mission is to contribute to product management activities from an engineering perspective, while also enhancing the technical proficiency of the GECIA team with a solution-oriented mindset Additionally, you will be responsible for ensuring on-time delivery and a first-time right approach in all your work Key Responsibilities Customer Focus - Study & Analyse Technical Specifications for Scope, Technical requirements and work content based on the inputs received - Generate 3D layouts, detail engineering and drawings for new deigns, Customised/ES Piston products and Skid Packages - Monit...

Background The Hans Foundation (THF), established in 2009, is a Public Charitable Trust that works towards creating an equitable society to enhance quality of life for all through the empowerment of marginalized and underprivileged communities in India. The Hans Foundation works for the Health and Wellbeing of remote and under-served groups, with an additional focus on children, persons with disabilities and women. THF also works for holistic Education and Livelihood development of our communities. Our Two-Fold Strategy involves identifying working within Aspirational Districts and high poverty index in the North, North-East and East regions within specific states, as well as catering to low...

Position: Deputy Manager- Liquid-Dielectrics Employment Type: Fixed Term Employment on ERDA Rolls for initially 03 Years, it will be regularized based on the performance Location: Makarpura, Vadodara Qualification: Essential: M. Sc. (Organic or Inorganic Chemistry) (Full Time) Desirable: Ph.D. in Organic or Inorganic or Polymer chemistry Experience Description ( Minimum 12 years to Maximum 18 years) Work experience in a testing laboratory or quality control department of industries in field of transformer oil testing involving following mentioned work areas Key Responsibilities 1. To plan and monitor the day-to-day activities of oil section 2. To achieve the revenue targets of section 3. To ...

Role Description: The Senior Manager Quality Compliance External Affairs will enhance quality, compliance, and regulatory flexibility by providing leadership and support of external activities impacting Amgens Operations function with link to Regulatory Affairs-CMC, with a regional focus on Japan & Asia Pacific (JAPAC). This role will shape, coordinate and provide input in the development of policy, regulatory requirements, and expectations consistent with Amgens position and priorities on GMP/GDP primarily in JAPAC and regarding related international organizations (e.g., APEC, ICH, Pharmacopoeias, PIC/S, WHO) in support for GCP, GLP, GPvP compliance, as requested. The senior manager will ex...