1381 Qms Jobs - Page 49

Ability to handle day to day maintenance and operation of Instrumentation maintenance with the help of engineers Good analytical skill and system approach to analyze the problems Ability to carry out corrective action after analysing frequent breakdowns in plant equipment Exposure in Handling of MSGL equipment, RVD, ANF and pumps with Mechanical seals Knowledge of QMS and ISO systems

Ability to handle day to day maintenance and operation of Instrumentation maintenance with the help of engineers Good analytical skill and system approach to analyze the problems Ability to carry out corrective action after analysing frequent breakdowns in plant equipment Exposure in Handling of MSGL equipment, RVD, ANF and pumps with Mechanical seals Knowledge of QMS and ISO systems

Experience: 3-4 Years Education: Diploma or degree in Mech. Eng. Or relevant field Location: Gonde Plant Develop audit plans, schedules, and objectives for Quality Management System (QMS) audits. Conduct internal audits of processes, departments, and functions to verify compliance with ISO 9001:2015 or other relevant standards. Review documentation, processes, and records to ensure accuracy and consistency. Maintain accurate records of all audit activities and follow-up actions.

Ensure that the organization s Quality Management System confirms to customer, internal, requirements. Ensure evaluation of, and reporting on,Customer quality requirements for root cause , and take relevant corrective measures with RD Project leading at supplier end for Controller/PCB Assembly build up from QC perspective Inprocess and EOL lines issues taking up with relevant department for RCA corrective measures Field issues related to controller taking up for RCA Corrective measures with internal electronics RD team as well with supplier as applicbale Oversee product recalls/Warranty Issue and line rejection Report to top management on the performance of the QMS,which shall include the need for improvement. Execution of new production development with RD department for Quality requirement for Inprocess/EOL Coordinating with RD department time to time for issues observed during QC checks for its resolution (Not hampering dispatched schedules) Continual improvement in Processes for increased efficiency, Employee engagement, customer satisfaction etc Reviewing the release DCR (Design change release) for controller from quality standpoint and taking up with RD for any queries before final release to production Participate in NPD activities from Quality perspective

Description Underground Cable Designer - Transmission Distribution: Experience in Design of Underground Power line projects using different software or relevant such as Civil 3D, MicroStation, ArcGIS. Role and Responsibilities: Prepare designs and drawings to be carried out in accordance with relevant codes of practice, standards, regulatory authorities, and clients requirements. Coordinate with lower-level drafting personnel. Support their mentorship and technical development. Delegate and oversee workload to lower-level drafting personnel assigned to projects. Perform documented quality reviews of drawing packages adhering to the terms of the quality management system. Provide specialist knowledge input and keep up to date with the latest developments in particular fields. Innovate and identify optimal methods to perform design tasks. Be willing to make the necessary travels to carry out project requirements. Coordinate with project engineering and project management teams to ensure timely and quality deliverables. Perform QA/QC reviews of pulling calculations, alignments, layers, design standards, and construction design packages. Promote the interests of the company, for example through personal contacts, representation in professional groups, contributions at meetings and the publication of material where opportunities arise. Qualifications Qualifications Diploma in Electrical/Civil with 3-4 years of experience OR ITI in Electrical/Civil with 6-8 years of experience. Underground experience a plus. Transmission or distribution experience preferred. Proven verbal and written communication and IT (office packages) skills. Track record in finding solutions to complex problems within deadlines. Experience leading a team of engineers and designers Managing mul7ple projects, deadlines, and deliverables in parallel Communica7ng with mul7ple teams and stakeholders Priority management and schedule planning. Knowledge of underground powerlines construction methods a plus. Knowledge regarding easements, right-of-way, and permitting considerations and impacts. Knowledge of creating plan profile drawings using Civil-3D or MicroStation. Able to handle multiple projects simultaneously and to prioritize work. Knowledge of utility telecommunications, distributed energy resource integration, and advanced distribution technologies a plus. Strong analytical capability. Flexibility to work in different roles for different clients both locally and worldwide. Traveling will be a considerable advantage. Capable of devising new approaches to problems encountered. Job Engineering Primary Location India-Karnataka-Bengaluru Schedule: Full-time Travel: No Req ID: 250718 Job Hire Type Experienced Not Applicable #BMI N/A

Hiring for Jr. Executive / Sr. Executive for RA - API with 2 to 5 Years of experience.

Roles & Responsibilities: Carrying out inspection of machined components from sub contract at incoming / inward stage and ensure the drawing dimension and providing a Usage Decision in the SAP system. Verify the inspection reports of machined components from sub contract and compare with component drawing and ensure the quality requirements. Co ordinating with suppliers for getting right components and educating process and inspection methods. Co ordinating with cross functional departments like SCM / Purchase, Stores, Production, TOP department in order to clear the items. Arrange PMI test for the received components and ensure the PMI result with standards and clear it for next process. Providing the inspection support work for Machine shop 1 & 2 Attend the assembly issues related to sub-contract machined components. Allocate the TPI to sub supplier end for daily inspection based on buyer inspection request. Item code Approval for approved supplier in SAP system based on the request from concern buyers. Raise X2 Notification for the deviations observed during machined component inspection and assign to concern buyer and ensure the rework activity and closure of notification after getting feedback. Prepare the dimension report for API related components. Qualification and Experience DME with 5 - 7 years and BE (Mechanical) with 3 - 5 years of experience in relevant Valve Industry. Functional Skills Product Knowledge Knowledge in QMS Inspection Knowledge on machined components Qualification in NDT- PT Knowledge in Visual Inspection Behavioural Skills Communication Skills Team work

Support Customers with Conflict Mineral Declarations. Follow up with Divisions for Corrective Action reports to address the Customer complaints and upload to Supply ON and other Customer portals. Upkeep Corporate Quality intranet portals. Preparation of periodical Corporate Quality reports, distribution and follow-up. Customer specific requirements - Handling of specification and coordinating with the Divisions What you will bring along: BE/B.Tech in Electronics / Electrical / Chemical / Mechanical Fresher - 0 to 1 Year experience Excellent coordination and communication skills. Knowledge of Electronic Components, Quality Management system. Problem-solving skills and the ability to handle pressure. Conversant to work on Microsoft Office.

Job Summary: The Radiation Safety Officer (RSO) is responsible for ensuring compliance with radiation safety regulations and guidelines in the auto components manufacturing industry. The RSO will oversee the safe handling, storage, and disposal of radioactive materials, primarily used in non-destructive testing (NDT), X-ray inspection, or other radiation-related applications in the plant. Key Responsibilities: Radiation Safety & Compliance: Ensure compliance with Atomic Energy Regulatory Board (AERB) and other relevant regulatory bodies. Develop, implement, and monitor radiation safety programs as per industry and government standards. Maintain records of radiation sources, exposure levels, and personnel monitoring data. Conduct periodic radiation safety audits and inspections within the plant. Training & Awareness: Provide training to employees on radiation safety, safe handling of radioactive sources, and emergency procedures. Conduct refresher training sessions for workers exposed to radiation in their work environment. Ensure all personnel working with radiation sources are equipped with personal dosimeters and trained in their use. Monitoring & Risk Assessment: Conduct radiation exposure assessments and ensure radiation levels remain within permissible limits. Investigate and document any radiation incidents or abnormal exposure cases. Establish protocols for handling radiation-related emergencies and conduct periodic drills. Equipment & Safety Measures: Ensure radiation shielding and protective equipment are in place and maintained properly. Monitor and calibrate radiation detection and measuring instruments. Supervise the proper storage, transportation, and disposal of radioactive materials. Regulatory Compliance & Documentation: Maintain and submit reports to regulatory authorities as required. Liaise with AERB and other relevant agencies for licensing, renewals, and compliance checks. Ensure radiation workers undergo periodic medical check-ups as mandated by regulatory standards. Skills & Competencies: Strong knowledge of radiation physics, safety regulations, and hazard management. Excellent training and communication skills for educating workers on radiation safety. Ability to conduct risk assessments and implement preventive measures. Detail-oriented with strong documentation and regulatory reporting skills. Work Environment: Exposure to radiation sources used in quality inspection or material testing. Regular interaction with production, quality, and safety teams. Occasional travel for compliance audits, training, and inspections.

Candidate should be Well versed in quality inspection of FRP Materials. Knowledge of Quality inspection procedure for ASTM,ISO,EN & IS standard. Knowledge of Quality tools like 7 QC,5 S, Kaizen etc. Use of Measurement & inspection tools. Knowledge of Composite product & Mfg. Process of pultrusion process. Reworks & Rejected data trace-out of all order in final product & ensure to product Traceability for each & every profiles ongoing order. Significant contribution in preparing documents for All running Project & handling of TPI Inspection. Position for Shift duties (three shift) working -8 hrs Supervision, Report generation and Planning with coordination with team. Knowledge of Computer & ISO documentation. Handling all Pultrusion project independently. Sincere & hard working for First article inspection of finish product materials. Follow All Safety guideline & Zero tolerance policy.

Description External Job Description Job Purpose Responsible for Internal Audit & Risk management Business Responsibility Areas Assess the adequacy and relevance of internal control systems, policies and procedures report on the extent of compliance with the same Provide reasonable assurance to the Audit Committee and Executive Council over efficiency/effectiveness of operations including safeguarding of assets, the reliability of financial and management reporting, and compliance with laws and regulations Conduct proactive fraud audits to identify potentially fraudulent acts participate in fraud investigations under the direction of fraud investigation professionals, and conduct post investigation fraud audits to identify control breakdowns and establish financial loss Qualifications 1st Attempt CA Previous Experience Relevant Post Qualification Experience in Internal Audit

PURPOSE OF THE JOB Apply and deploy Serial Supplier Quality Assurance policy in collaboration with Procurement. Responsible for Non-Conformity Report management and Supplier performance for a precise scope of suppliers/projects, after the product validation, the First Article Inspection (FAI) + 3 deliveries. Perform inspections for low-critical parts Manage Quality performance of assigned Suppliers Manage Incoming Inspection activities when appointed SQ inspection leader for the given site ORGANISATION Organization structure (job belongs to) Site location/Quality/Supplier Quality Reports directly to Supplier Quality Manager Site (QC-SQ-01) Internal Procurement, Supplier Quality Industrial organization, Industrial Quality Supply chain External Suppliers Sub-contractors MAIN RESPONSABILITIES Depending on the size of the site and the teams to be managed, roles and responsibilities described below can be assigned to one person or split over several SQ Serial engineers. There must be one single person in charge of leading incoming inspection (one single interface towards Industrial), which can have also the SQ Serial Performance management role. SQ Serial Performance management Non- Conformities Management: Responsible for Non-Conformity day-to day management, insuring reactivity to inform supplier of Non-Conformity Report (NCR), to replace defective parts and to implement securization. Animate Non-Conformities Report treatment by setting-up relevant actions plan to reach Non-Conformity Report (NCR) target. Invoice the Cost Of Non-Quality (CONQ S1) to the suppliers. Ensure management of Suppliers waiver requests for assigned scope and Suppliers Containment actions: Organize the retrofit to be performed by the supplier. Decide quality wall if necessary. Solving issues & Continuous Improvement: Secure in a timely manner strong and complete supplier containment actions plan to secure the Manufacturing line Challenge our suppliers to enforce relevant corrective and preventive action plan, challenge reactivity. Check the effectiveness of the corrective and preventive action plan of the Supplier, ask for evidences, challenge them and perform suppliers visit. Ensure control plan sustainability (regular follow-up on main suppliers). Set up and manage Supplier improvement roadmap for non-performing Suppliers according to Supplier Quality escalation process (Green / Yellow / Red status) Organize reviews with suppliers and visit suppliers premises as necessary. Inspection of low-critical parts: Ensure performance of inspection for low critical parts (parts non-included Supplier Part List) Check the effectiveness of the corrective and preventive action plan of the supplier (ask for evidences, challenge them, and perform suppliers visit do supplier visit). Ensure control plan sustainability (regular follow-up on main suppliers). For trusted suppliers: to take part of the Return Of experience (REX) analysis. Top Issues Dashboard: Prepare and monitor supplier Quality review at unit level to tackle the Top issues. Incoming inspection leader The Incoming inspector Leader ensures the compliance of purchased products and parts delivered to the ALSTOM facilities. He / She manages the team of Incoming Inspectors to ensure consistent, accurate and on-time completion of incoming inspection activities. Accountabilities & Authorities: Manage day-to-day Incoming Inspection Activities: Collaborate with SPQD, SQ Serial Engineers and Incoming Inspectors to ensure Control Plans are defined and registered in the ERP system Ensure appropriate control keys (and rules associated) are implemented in the ERP system, with clear and documented sampling rules, dynamically defined and updated. Ensure inspection instructions/ checklists are defined and available for Incoming Inspectors Establish and manage the process for maintaining and storing records at Incoming Inspection Ensure Incoming Inspectors comply with procedures for inspection, tool calibration, storage of records, NCR characterization and ERP transactions. Initiate outside special process inspections or outside lab testing when required Ensure control plans are modified when NCRs are detected at incoming and on the production line Inform SQ Serial and Supply Chain on defects detected at Incoming (Non-conformities opened) and impact on part availability Schedule daily meetings to share daily priorities and manage daily workload of Incoming Inspectors Maintain and publish KPIs and identify opportunities for performance improvement Incoming Inspection team competencies management through skills matrix and scheduling trainings when required Performance measurements: Complete inspections within allocated target lead time and ensure priority inspections are completed on time Accuracy and correct defect characterization in Non-conformities and related ERP tasks (blocking stock, tasking, etc.) Ensure set up and implementation of continuous performance improvement actions with a regular analysis of downward trend in quantity of NCRs detected after incoming inspection during the production cycle (non-functional issues only) Manage Incoming Inspection activities when appointed SQ Referent for the given site LOCATION & MOBILITY: Site and travel to suppliers site for SQ Serial Engineer / Professional MAIN REQUIRED COMPETENCES Educational Requirements Mandatory: Bachelors degree in Quality or Engineering or equivalent Familiar with supplier qualifications standards (ISO, ASME, IRIS, Local Standards, etc.) Fluent in English Desirable: Masters degree in Quality or Engineering or equivalent Experience Mandatory: 1 to 3 years experience in Quality, Production Knowledge in a technical field Desirable: Experience managing supplier relationships is a plus Experience using SAP or similar computer applications Competencies & Skills See related Quality & Continuous Competencies Matrix 8D Methodology Collaborative Persuasive and resilient

We are hiring for one of our Leading client for QMS Engineer for Bangalore. Total experience - Minimum 4 Years in Automotive industry, EV chargers etc. Location - Bangalore (Whitefield) Job Description: I. Experience • Establish the quality policy • Ensure quality objectives fit the strategic direction • Ensure QMS requirements are integrated into the organisation business processes • Ensure resources needed for the QMS are available • Communicating the importance of the QMS requirements • Engaging, directing and supporting people to participate in the QMS • Ensure customer and legal requirements are met • Ensure that risks and opportunities are identified and addressed • Assign responsibility for the QMS, its processes, reporting, and for managing change • Review the QMS at planned intervals • Provide manufacturing floor support relative to process trouble-shooting and on the job training • Work with the Plant Manager and department heads to develop forward thinking plans to grow the effectiveness of the Quality System • Monitor Cost of Quality results and engineer changes which will help the plant surpass COQ objectives • Directly and through subordinates, effectively oversee traditional Quality Control functions • Restricting products from shipment, as necessary, in accordance with established procedures • Communicating with customers, other plants, and with consumer affairs and field sales, to resolve problems reported II. knowledge • Automotive business process approach knowledge • ISO, IATF, EHS PPAP, MSA, SPC - Knowledge • AIAG CQI 17 Soldering process (reflow, wave) - Knowledge • SMT process knowledge (PCBA, PCB, IPC standards) • SMT part testing knowledge (ICT, FCT, AOI, EOL) • Problem solving (8D) - Knowledge. • Interpretation of 2D & 3D drawing & technical specification - knowledge III. Education • Bachelor of Engineering (B.E) Electrical /Electronics / Equivalent

Job Purpose The John Cockerill Group, a world leader in Green Hydrogen technologies has established itself as a reliable partner for all the stakeholders aiming to achieve Net zero emission targets. We are present across geographies and in all key energy markets. Our mission is to accelerate the transition to green hydrogen for a carbon-neutral world. We are a recognized leader globally for large-scale decarbonized hydrogen production solutions. John Cockerill Hydrogen (JCH2) has Global footprints and to supports its International and domestic operations we are looking for an Electrical, Automation & Instrumentation Manager (EAI-M) to be based in Mumbai (India) office. The EAI-M will be responsible for planning, leading, and providing engineering/technical support for a large Projects. Needless to mention, the EAI-M will be a key member of JCH2 team to achieve operational excellence and support the growth objectives of the organization globally. Electrical, Automation & Instrumentation Managers currently having experience in in EPC / Design engineering organizations with similar profile in oil & gas/Energy/Heavy engineering space would be preferred. Key Result Areas Lead a multi-disciplinary (Inhouse or Engineering subcontractor s) engineering team for successful execution of Green Hydrogen product development and project follow-up (from FEED to Plant start-up & client handover) with in predefined schedule and cost budget. Lead and mentor a growing team of engineers and technicians, fostering their professional development and aligning their skills with business needs. EAI-M will work in tandem with Headquarter EAI-M and acts as a primary interface point between John Cockerill (JCH2) Indian team and John Cockerill Global teams, being technology and execution team, or local partner, vendors, Engineering subcontractors, and client for seamless flow of information and on time technical resolutions. Key Responsibilities Responsible for electrical design for feeding stacks (AC/DC conversion). Responsible for the design of all instrumentation, cabling and control philosophy for each product. Responsible for electrical design in EPC projects. Oversee and coordinate resources within in-house EAI team, responsible for the team load management. In cooperation with EAI-M, develop product roadmaps, guidelines for projects and standardize studies. Technical point of contact with the customer and other internal & external stakeholders of the project. Finalizing the requirements of applicable local, international, regional rules & regulations - key focus on Ex rules. Finalize the list of applicable codes and standards to be followed for the FEED & Detail engineering phase of projects. Define requirement of engineering software s, tools, and methods for completion of engineering. Define the engineering scope split between in house engg teams and external engineering subcontractor as applicable. Define list of documents to be submitted for PMC/Client approval. Finalize list of packages, equipment s etc. falling on critical milestones and prepare a schedule for their ordering. Finalize list of vendor document for each package /equipment s required in Information and approval category. Lead and organize technical review Education and Experience Graduate in Electrical, Instrumentation, Power Electronics or Automation Engineering from a reputed university. Post-graduation will be an added advantage. 10 to 15 years experience in large engineering / project / process / heavy engineering industry with an exposure to Multinational environment. Good process background Experience in the Oil&Gas sector is a competitive advantage, including relatives codes & standards Background, Skills, and Competencies Identification and management of technical risks Solution-oriented with a high capacity to collaborate with all types of profiles. Compliance with the internal quality management system Compliance with norms, internal standards, as well as specific customer requirements Autonomous profile, able to take initiative, to work in a team with multiple interfaces related to various areas of expertise. Able to handle a variable workload (some very busy periods with multiple projects in parallel) Proactivity in the implementation of technical continuous improvement processes, based on feedback. Good exposure and understanding of PESO norms. Knowledge of International Standards such as IEC / ATEX / UL Should have managed the complete process of Engineering Change Management Fluency in English is mandatory, and knowledge of French is added advantage.

Take actions to improve on time delivery, quality, and customer satisfactionTrack and monitor the progress of numerous customer orders and partner jobs. Provide excellent customer and partner service by building relationships, creating partnerships, and by providing frequent and timely customer interactions on order updates Apply first-hand technical knowledge (or leverage other subject matter experts) on manufacturing design and production to ensure jobs are delivered on time. Understand supplier capabilities and execute supplier oversight activities, which include frequent phone assessments, detailed schedule creation, quality reviews, and supplier corrective actions. Assess the impact of manufactured part rejections; communicate with suppliers and customers to work through problems and resolve cases. Manage customer complaints that result in replacements for returned products Report out on status, risk, and efforts to recover troubled orders and jobs. Job Duties Document all case activity in the central database. Leverage company technology platforms and comply with the Quality Management System Monitor the integrity of supplier quality metrics. Interface with Engineering, Customer Care, Quality, Sales, and Shipping teams to ensure manufacturing processes are capable of customer on-time delivery and satisfaction. Effectively communicate with all key stakeholders, including suppliers, customers, and leadership. Participate and provide input on initiatives to simplify and automate complex processes. Perform all work in compliance with Xometrys quality and safety systems, policies, and procedures. Qualifications Prior project management, supply chain, and customer service experience are required. A minimum of 3 years of related experience, preferably in manufacturing or operations A Bachelor of Science Degree in Supply Chain, Engineering, or a technical related field is preferred. Working knowledge of and/or education, skills, and experience associated with manufacturing processes, engineering drawing requirements, and mechanical and electrical inspection methods. Capable of performing root cause analysis and identifying solutions to complex problems. A self-starter who can work independently and can drive actions to completion. Strong organizational skills and the ability to work in a dynamic environment. Able to multitask, meet deadlines, and support all supplier quality field activities. Strong communication skills (both oral and written) + ability to manage up and to the side. Education, including special education A Bachelor of Science Degree in Supply Chain, Engineering, or a technical related field is preferred. Working knowledge of and/or education, skills, and experience associated with manufacturing processes, engineering drawing requirements, and mechanical and electrical inspection methods. Special work experience required A minimum of 3 years of related experience, preferably in manufacturing or operations Personal qualities Capable of performing root cause analysis and identifying solutions to complex problems. A self-starter who can work independently and can drive actions to completion. Strong organizational skills and the ability to work in a dynamic environment. Able to multitask, meet deadlines, and support all supplier quality field activities. Strong communication skills (both oral and written) + ability to manage up and to the side Language skills English C1

About Company: Alkem MedTech Pvt Ltd is a wholly owned subsidiary of Alkem Laboratories Ltd, which is the 5th largest listed Pharmaceutical company in terms of market share. As the first MedTech venture of Alkem Labs, Alkem MedTech is dedicated to advancing precision, high-risk, and implantable medical devices along with their accessories. MedTech is a strategic priority for Alkem Labs, representing a significant growth avenue. We are beginning our MedTech journey by focusing on Musculoskeletal solutions and have plans to expand into multiple segments, establishing a robust, multi-faceted MedTech company in the near future. Alkem MedTech will be manufacturing in India, aligning with the vision of the Government of India to boost domestic production and innovation in the medical technology sector. We are looking for passionate and innovative talents to join our pioneering team. If you are excited about shaping the future of medical technology and want to be part of a transformative journey, Alkem MedTech is the place for you. Why Join Us? Innovation-Driven Environment : Work on cutting-edge technologies in precision and implantable medical devices. Growth Opportunities : Be part of a strategic growth initiative for one of the leading pharmaceutical companies and be part of creating a legacy. Collaborative Culture : Engage with a team of dedicated professionals committed to making a difference in healthcare. Impactful Work : Contribute to life-changing medical solutions in the Musculoskeletal segment and beyond. Manufacturing in India : Support the vision of the Government of India by contributing to domestic production and innovation in the MedTech sector. Join us at Alkem MedTech and help shape the future of healthcare technology. Purpose of the role: The Warehouse Supervisor is responsible for overseeing the efficient operations of the warehouse, ensuring the safe storage, handling, and distribution of orthopedic products, including implants, surgical instruments, and related medical supplies. This role requires leadership, organization, and attention to detail to maintain an accurate inventory, comply with regulatory requirements, and ensure the timely delivery of products to customers or healthcare providers. Roles & Responsibilities: Warehouse Operations: Supervise daily warehouse activities, including receiving, storing, inventory management, and shipping of orthopedic products. Ensure that products are stored in the correct locations, utilizing proper handling techniques to avoid damage and maintain quality. Oversee the picking, packing, and shipment of orders, ensuring that they are accurate and meet customer specifications. Implement and enforce safety protocols to ensure compliance with OSHA, FDA, and other relevant regulations governing orthopedic products. Inventory Management: Maintain accurate inventory records, tracking product levels, movements, and stock rotation. Perform regular physical inventories and reconcile with the warehouse management system (WMS) to prevent discrepancies. Ensure proper labeling, barcode scanning, and tracking of all orthopedic products to facilitate easy identification and efficient stock rotation. Regulatory Compliance & Quality Control: Ensure compliance with industry standards, including FDA, GMP (Good Manufacturing Practices), and other regulatory bodies governing the storage and handling of orthopedic products. Maintain cleanliness and organization within the warehouse to comply with regulatory requirements and avoid cross-contamination or damage to products. Monitor and ensure that products are handled, stored, and transported according to established guidelines to maintain their integrity and prevent product recalls or errors. Conduct routine inspections to verify product quality and document any defects or discrepancies. Shipping & Receiving: Oversee the receiving process, ensuring that incoming shipments are inspected for accuracy, quality, and condition. Coordinate the timely shipping of orders to customers, distributors, and healthcare facilities, ensuring compliance with delivery deadlines and customer expectations. Maintain relationships with shipping carriers to ensure cost-effective and efficient transportation of products. Process Improvement & Efficiency: Identify opportunities for improving warehouse processes, reducing errors, and increasing overall efficiency. Implement best practices in warehouse management, including the use of technology such as barcode scanners, RFID, and warehouse management systems (WMS) to streamline operations. Monitor performance metrics and take corrective actions as necessary to meet operational goals related to order accuracy, inventory turnover, and shipping times. Health and Safety: Ensure the warehouse operates in a safe and efficient manner by enforcing workplace safety standards and OSHA guidelines. Conduct safety audits and risk assessments regularly to identify and mitigate potential hazards. Ensure that all warehouse equipment (e.g., forklifts, pallet jacks) is properly maintained and operated by certified staff. Reporting & Documentation: Maintain accurate records of inventory transactions, shipping and receiving activities, and any incidents that occur within the warehouse. Prepare and present regular reports on inventory levels, warehouse performance, and any operational issues to senior management. Ensure proper documentation is maintained for regulatory compliance, product traceability, and audits. Education background: BE / BTech preferred Preferred Experience (Industry/therapy/function no. of years): 4-5 years of experience in the MedTech, Pharma industries Competencies: Proficiency in SAP MM, SAP WMS, Bin Management System, QMS ( NC & CAPA) Personal Attributes: Self-motivated and proactive. Ability to handle stress and maintain a calm demeanor. Flexible and adaptable to changing priorities.

Job Purpose "This position is open with Bajaj Finance ltd." Duties and Responsibilities Duties and Responsibilities:Role: Work as part of the audit team for one of the most prestigious & rapidly growing fintech company in India Conduct Internal Audit for BFL & other group companies with special focus on IT domain; under supervision of National Lead / Chief Corporate Audit Work jointly with dynamic team of ~20 professionals with varied experience Scope: Cover specific domains as- IT General Controls (ITGC):IT infra, Cloud, DC, User Assets IT Security:Information security, cyber security, Change management & SoD controls Fintech technologies:RPA, BOT, API, Mobile Apps, Website controls Platform review:Technical & Functional controls in core platforms like SFDC, FinnOne, Pennant, Finnacle, SAP & other apps Review other allied business processes in lending business like consumer loans, business loans, commercial loans Support IT reviews in other group entities like holding company, investment company & insurance companies. Required Qualifications and Experience Required Qualifications:Qualifications: BE/BTech 2-4 years of experience in reputed companies / big consulting firms in Technology Risk domain CISA / CISSP / CISM is strongly recommended Strong domain knowledge of information technology areas & its impact on business processes in BFSI sector Leadership Skills: High motivational levels and need to be a self-starter Ability to grasp/ learn and unlearn processes Excellent oral and written communication, analytical skills, clarity of thoughts and perseverance. Demonstrated success & achievement orientation

Biocon Biologics is a subsidiary of Biocon Ltd, an innovation led global biopharmaceuticals company. Biocon Biologics is engaged in developing high quality, affordable biosimilars that can expand access to a cutting-edge class of therapies to patients globally. It is uniquely positioned as a fully integrated pure play’ biosimilars organization in the world and aspires to transform patient lives through innovative and inclusive healthcare solutions. The Company has a large portfolioof biosimilars under global clinical development with three of these commercialized in at least one of the developed markets of EU, U.S. and Japan. Biocon Biologics has a product pipeline of 28 molecules, including 11 with Mylan, severalwith Sandoz and is developing many independently. BioconBiologics believes that strong partnerships offer enormous opportunities to co-create the future of healthcare, building a patient ecosystem beyond the product, which can transform millions of lives. Job Level: Associate Manager - IT quality and Compliance Location: Bengaluru (Jigani Link Road) Job Type: Full-Time Experience Required: 5-6 years in Life Sciences with 3-4 years in IT Job Description: Ideal candidate will have a strong background in the life sciences domain, with hands-on experience in the validation of scientific applications such as Laboratory Information Management Systems (LIMS) and other laboratory instruments Key Responsibilities: Lead and manage the validation processes for scientific applications, ensuring compliance with industry standards and regulations. Collaborate with cross-functional teams to implement and maintain LIMS and other scientific applications. Provide technical expertise and support for the integration and optimization of scientific applications. Develop and execute validation protocols, test plans, and reports. Ensure data integrity and security within scientific applications. Troubleshoot and resolve issues related to scientific applications and their interfaces. Stay updated with the latest trends and advancements in life sciences and IT. Qualifications: Bachelor’s or master’s degree in Life Sciences, Biotechnology, Bioinformatics, or a related field. Overall experience of 9+ years of employment tenure. 5-6 years of experience in the life sciences domain. 3-4 years of experience in IT, specifically in the validation of scientific applications. Strong knowledge of LIMS and other scientific applications. Excellent problem-solving and analytical skills. Strong communication and interpersonal skills. Ability to work independently and as part of a team. Preferred Skills: Experience with regulatory compliance (e.g., FDA, EMA). Knowledge of GxP, 21 CFR Part 11, and other relevant regulations. Familiarity with project management methodologies. Review operations and related controls provide assistance to Author applicable SOPs governing the CSV processes for BBL IT Equal Opportunity Employer Biocon Biologics is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Biocon Biologics also complies with all applicable national, state and local laws governing non-discrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act.

Job Overview: Electrica Engineers Pvt Ltd is seeking an experienced Senior Manager to lead the Quality Department . A strong background in the Automotive Lighting industry and Quality Management Systems is required. The ideal candidate will improve Quality Assurance policies , Develop Product and Process Guidelines , and ensure Operational Efficiency . Key responsibilities include managing Customer complaints , handling Audits , driving Continuous Improvement , and maintaining Compliance with Industry standards . Key Responsibilities : Process and Product Quality Management: Collaborate with relevant departments (Engineering, Manufacturing, Supply Chain, etc.) to establish and maintain quality standards for both processes and products. Define acceptable quality metrics aligned with customer requirements, focusing on key performance indicators (KPIs) like PPM and defect rates. Quality Result Indicators Accountability: Achieve and monitor quality targets such as customer PPM, zero repetitive quality concerns, and eliminate customer line stoppages due to quality issues. Regularly report on quality performance and implement corrective actions as necessary. Compliance with IATF16949 Quality Management System: Ensure adherence to the IATF16949 standard, providing support for audits and maintaining system documentation to guarantee compliance. Customer Complaint Management: Analyze and resolve customer complaints using the 8D methodology, ensuring effective communication with customers and follow-through on corrective actions. PPAP Documentation: Prepare and review necessary documentation for the Production Part Approval Process (PPAP), Including Layout Reports, SPC, MSA, and Checking Aids, ensuring Customer and Regulatory Compliance. Rejection Data Analysis: Collect and analyze monthly rejection data, using quality tools (e.g., Pareto analysis, Fishbone diagrams) to identify process failures and implement corrective measures. Scorecard Performance Analysis: Perform detailed cause analysis of scorecard results, develop action plans, and implement corrective measures to improve performance and meet quality targets. Regulatory Compliance (Customer Standards): Ensure compliance with customer-specific standards and regulatory requirements such as IMDS, ROHS, ELV, REACH, Thermal Cycle, Identification Marking, and Flammability. Warranty Data and Trend Analysis: Analyze warranty data to identify new potential issues, follow up on 3MIS, and collaborate with cross-functional teams to address root causes. Use of Quality Tools: Utilize advanced quality management tools and techniques such as SPC, PPAP, Control Plans, FMEA, Poka-Yoke, 7 QC Tools, MSA, and others to monitor and improve quality performance. Desired Qualifications : Education: Bachelor's degree in Engineering, specializing in Electronics & Telecommunications (E&TC), Mechanical Engineering, or a related field. Experience: Minimum of 14 -20 years of experience in the Automotive or related Engineering Industry. Proven experience handling Original Equipment Manufacturers (OEMs) such as TATA Motors , SAVW , Mahindra & Mahindra (M&M) , Bajaj Auto , Piaggio , Nissan , Stellantis , or similar. Experience in Automotive Lighting is preferred. Key Skills : Analytical Skills: Strong ability to analyze data, perform root cause analysis, and resolve quality issues. Problem-Solving: Ability to identify quality challenges and develop effective solutions. Quality Problem-Solving: Expertise in identifying and resolving complex quality issues within the manufacturing process. Team Leadership: Proven experience leading and motivating quality teams to meet goals. Communication Skills: Excellent verbal and written communication skills, with the ability to interact with cross-functional teams and customers. Customer Complaint Management: Experience managing customer complaints, ensuring timely resolutions and customer satisfaction. Regulatory Compliance: In-depth knowledge of industry standards and regulatory requirements (e.g., VDA 6.3 certification, IATF 16949). Root Cause Analysis: Expertise in conducting root cause analysis and implementing effective corrective and preventive actions. Continuous Improvement: Focused on driving continuous improvement through process optimization and quality initiatives. Quality Audits: Experience conducting or managing quality audits (including VDA 6.3 Certification and IATF 16949). Training Development: Experience developing and delivering quality training programs for internal teams. Quality Documentation (CP, PFMEA, MSA, SPC): Expertise in maintaining and updating quality-related documentation, including Control Plans (CP), Process Failure Mode and Effect Analysis (PFMEA), Measurement System Analysis (MSA), and Statistical Process Control (SPC). Customer Complaint Management: Skilled in managing and resolving customer complaints effectively to ensure high customer satisfaction. Quality Management Systems (e.g., IATF 16949): Proficient in the implementation and maintenance of quality management systems, including IATF 16949. Automotive Industry Knowledge: In-depth knowledge of the automotive industry, including standards, regulations, and best practices for quality assurance. Capabilities & Desired Characteristics : Lead & Collaborate : Lead and/or collaborate with cross-functional teams and departments to ensure expedited closure of complex product and process quality issues from initiation to closure. Technical Expertise : Act as a technical expert to lead IATF16949, ISO9001, VDA QMS audits. Implement procedures and best practices per industry QMS standards. Problem-Solving : Facilitate the use of structured problem-solving tools in root-cause investigation and corrective action identification. KPI Management : Create and manage KPIs, ensuring clear communication and expectations with factories for timely improvement plans. Collaboration & Prioritization : Ability to work collaboratively with cross-functional teams and handle multiple tasks while prioritizing effectively. Product Improvement : Develop and execute product improvement processes for the resolution of various quality issues and coordinate with other departments for the development of new products as per APQP & PPAP standards. Quality Improvement Cell : Build a cross-functional Quality Improvement Cell for constant review of processes and develop solutions to improve efficiency and reduce waste. Root Cause Analysis : Experience with root cause analysis and corrective actions. Organizational Skills : Strong organizational and time management skills. Employee Benefits : 1. Comprehensive Health Insurance: We prioritize the well-being of our team by offering comprehensive health coverage, ensuring peace of mind for you and your family. 2. Professional Development Opportunities: At Electrica, we believe in continuous learning. We provide access to training programs, workshops, and certifications to help you grow in your career. 3. Work-Life Balance Support: We promote a healthy work-life balance through flexible working hours and paid time off, ensuring you have time to recharge and focus on what matters most.

Hello Candidate, Greetings from Hungry Bird IT Consulting Services Pvt Ltd. We are hiring Production Manager - API Manufacturing for our client a leading pharmaceutical manufacturing company dedicated to API/Intermediate. Company: Leading Pharmaceutical API Production Company Location: 1) Hyderabad, 2) Visakhapatnam About the Company: Active Pharmaceutical Ingredient manufacturing company, robust product portfolio spread over major product segments encompassing Expectorants, Muscle Relaxants, Analgesic and Anti Fungal. Job Description We are seeking a highly skilled and experienced Production Manager to oversee the production operations of our Active Pharmaceutical Ingredient (API) manufacturing facility. The ideal candidate will have a deep understanding of API manufacturing processes, particularly in the areas of expectorants, muscle relaxants, analgesics, and anti-fungal APIs. Key Responsibilities: Production Planning and Scheduling: Develop and implement comprehensive production plans and schedules to meet customer demands and optimize resource utilization. Monitor production progress and adjust plans as needed to ensure timely delivery. Process Optimization: Continuously evaluate and improve existing production processes to enhance efficiency, reduce costs, and improve product quality. Implement innovative technologies and techniques to optimize production yields and minimize waste. Quality Assurance: Ensure strict adherence to cGMP, ISO, and other relevant regulatory standards. Oversee quality control procedures, including sampling, testing, and documentation. Collaborate with the Quality Assurance team to identify and resolve quality issues promptly. Team Management: Lead and motivate a team of production personnel to achieve production goals. Provide training and development opportunities to enhance employee skills and knowledge. Foster a positive and collaborative work environment. Regulatory Compliance: Stay updated on regulatory requirements and industry best practices. Ensure compliance with all applicable regulations, including FDA, EDQM, and WHO guidelines. Prepare and submit regulatory documentation as required. Safety and Environmental Compliance: Implement and enforce strict safety protocols to minimize workplace accidents and injuries. Promote a culture of safety and environmental responsibility. Ensure compliance with environmental regulations and waste management guidelines. Troubleshooting and Problem-Solving: Identify and troubleshoot production issues, such as equipment malfunctions, process deviations, or quality problems. Implement effective solutions to minimize downtime and maximize productivity. Qualifications and Experience: Bachelor's or Master's degree in Pharmacy, Chemical Engineering, or a related field. Minimum of 10 years of experience in API manufacturing, with a strong focus on expectorants, muscle relaxants, analgesics, and anti-fungal APIs. In-depth knowledge of API manufacturing processes, including synthesis, purification, and formulation. Strong understanding of cGMP, ISO, and other regulatory requirements. Proven track record of leading and managing production teams. Excellent problem-solving, decision-making, and analytical skills. Strong communication and interpersonal skills. Ability to work under pressure and meet tight deadlines. If you are a highly motivated and experienced Production Manager with a passion for API manufacturing, we encourage you to apply. (Interested candidates can share their CV to krishna@hungrybird.in or call on 9966952299.) Please furnish the below-mentioned details that would help us expedite the process. PLEASE MENTION THE RELEVANT POSITION IN THE SUBJECT LINE OF THE EMAIL. Example: KRISHNA, HR MANAGER, 7 YEARS, 20 DAYS NOTICE Name: Position applying for: Total experience: Relevant Experience: Notice period: Current Salary: Expected Salary: Thanks and Regards Krishna +91 9966952299

Role & responsibilities 1. To maintain and ensure the cGMP compliance. 2. Preparation of MPCR, PVP, PVR, HSP & HSR based on TTD. 3. Preparation of proposed commercial MPCR based on marketing requirements. 4. Raw material tracking for the smooth functioning and timely execution of the products. 5. QMS related activities (CRF/Deviation/Investigation/CAPA) and compliance. 6. Follow up for CRF approval. 7. Creation of HALB code and preparation of BOM in SAP 8. Compilation of validation documents like Process validation report and Hold time study report. 9. Any other job assigned time to time by superiors. Preferred candidate profile US Market experience in ANDA filing, CMC documentation, regulatory compliance, and technology transfer. Perks and benefits As per company policy

QA Head Foundry Overview : QA Head must Have Good Knowledge in All Foundry Proces, Machining Activities & Experience in Handling Automotive Customers, He Should Work Closely In The Various Department For Analysis & Reduction of Rejection & Customer Complaints , He will be Responsible for Handling All Types of Audits, Documentation , by Creating System Across Departments Experience : 15/20Yearas Education- DME/BE Mech, Metallurgy Skills : a) Experience in SG & CI iron (FOUNDRY)Casting Manufacturing b) Experience in All Foundry Process c) Familirity with ( IATAF& ISO) QMS & IMS Customer Specific Requests d) Knowledge of Foundry Defects & Remedies e) Proficiency in Data Analysis & Use of Different Softwares f) Fluent English Communication & Interpersonal Skills Key Responsibilities : a) Process Control in All Departments b) Customer Handling CAPA , 8D Submission c) Familirity with ( IATAF& ISO) QM & LMS Customer Specific Requests d)Overall Quality Management e) APQP, PPAP Documentation & Execution f) COPQ & COQ Analysis & Overall Management g) Final Quality Inspection Including Dimenstion of NDT etc h) Planning & Execution of Various Activities at All m/c Vendors i) Rejection Review Analysis & Taking Corrective Action j) Laison with Different Calibration Bodies & Arranging Audits Personal Attributes: a) Highly Oragnised & Detail Oriented b) Proactive & Self Motivated c) Strong Team Working & Collabrative Capablity d) Adaptive & Open to Change

Job Title: Quality Manager Aerospace Industry Company: Senwell Exports Private Limited Location: Wagholi Kesnand, Pune Industry: Aerospace Manufacturing Experience: 10 to 20 Years About Us: Senwell Exports Private Limited is a leading aerospace manufacturing company committed to delivering precision-engineered components that meet the highest industry standards. We are looking for a dynamic Quality Manager who can drive excellence, ensure compliance, and elevate our quality standards to global benchmarks. Key Responsibilities: Quality Assurance & Compliance – Establish and enforce AS9100 & ISO 9001 quality management systems to ensure aerospace regulatory compliance. Process Optimization – Develop and implement quality control procedures for CNC, VMC, and precision machining processes. Root Cause Analysis – Identify, analyze, and resolve quality issues using 8D, FMEA, CAPA, and Six Sigma methodologies. Supplier & Vendor Quality – Oversee supplier audits, evaluate materials, and ensure adherence to aerospace quality standards. Customer Satisfaction – Lead quality assurance initiatives to meet client specifications and enhance product reliability. Team Leadership – Guide and mentor the quality team, fostering a culture of continuous improvement and operational excellence. Requirements: Experience: 10+ years in quality management within the aerospace, defense, or precision manufacturing sector. Expertise in Standards: Strong knowledge of AS9100, ISO 9001, NADCAP, and aerospace regulatory requirements. Technical Proficiency: Familiarity with CNC/VMC machining, GD&T, metrology, CMM, and SPC tools. Problem-Solving Skills: Proven ability in root cause analysis, risk assessment, and quality failure resolution. Strong Leadership: Ability to drive cross-functional quality initiatives and collaborate with production, design, and supply chain teams. Why Join Us? Work with an industry-leading aerospace manufacturer shaping the future of precision engineering. Be part of a dynamic team committed to world-class quality and innovation. Competitive salary, career growth opportunities, and exposure to cutting-edge technology.

Roles & Responsibilities - Support Quality Management Systems (QMS): Assist in developing, implementing, and maintaining QMS, ensuring compliance with industry standards and certifications. Quality Control and Assurance: Oversee quality control operations, perform inspections, and ensure products meet quality standards. Process Improvement: Identify process improvement areas, implement corrective actions (CAPA), and promote continuous improvement. Non-Conformance Management: Manage NCRs, identify root causes, and ensure corrective actions are implemented. Customer and Supplier Quality Management: Ensure suppliers meet quality standards, review supplier performance, and address customer complaints. Support New Product Introduction (NPI): Participate in quality assurance for new products, conduct reviews, and ensure quality standards during scaling. Qualification Must having Batchelors Engineer Graduate (BE) with 10-12 years relevant experience of quality management.

Preferred candidate profile: The ideal candidate would be a person who takes complete ownership of the department, performs and guides the team to perform their responsibilities to achieve the targets set by management. They must be able to continue to strive to improve the relationship with the customer through providing the right quality product and ensure ZERO rejections at the customer end by implementing systems and process to reduce the overall PPM inside the plant and thereby ensuring that the customer is satisfied with our quality focus. Proven experience as Quality Manager Conscientious and responsible A keen eye for detail and a results driven approach Outstanding communication skills Excellent organizational and leadership skills Proficient in MS Office In depth understanding of quality control procedures and relevant legal standards Excellent math abilities and working knowledge of data analysis/statistical methods Candidate having an MBA degree is a strong advantage. Certification of quality control is a strong advantage (IATF16949) Knowledge of SAP QA Module is also an advantage. Role & responsibilities: Heading the entire plant quality control & assurance activities Implementation and maintenance of QMS throughout the plant Customer handling for quality related queries Regular customer visits Customer complaint handling Supplier audit Internal rejection reduction Incharge of COPQ Maintaining TS 16949 system Customer audit NPD quality, PPAP, FMEA, CP, PFMEA, Poka yoke Setting up and training quality team Supervising and reviewing daily activities of QMS Preperation of annual budget for the dept and ensuring the compliance Managing the Quality lab , MSA, Gauge R&R Cost saving, Kaizens, etc Perks and benefits: Company offers various benefits to employees who become confirmed like education assistance for their children, health insurance for the family, etc. Food is provided by the company.