We are looking for a strategic and proactive Chief Operating Officer (COO) to lead and expand the full spectrum of operations for B2B jewellery business. This role encompasses oversight of manufacturing, supply chain, logistics, compliance, and client delivery, with a focus on driving operational excellence, optimizing costs, and delivering exceptional service to its global wholesale and corporate clientele. Location : Mumbai Key Responsibilities Design and implement business operations to support scalable, efficient, and high-quality delivery of jewellery products to B2B clients. Translate the companys strategic vision into actionable operational plans and KPIs. Oversee jewellery production processes to ensure timely delivery, quality control, and cost-effectiveness. Manage vendor partnerships, outsourcing units, and in-house manufacturing teams. Optimize the sourcing of raw materials (precious metals, gemstones, packaging). Build strong supplier networks with a focus on sustainability, ethical sourcing, and reliability Work closely with the sales team to ensure smooth onboarding, order processing, and delivery for wholesale clients Collaborate closely with the Sales leadership to align operational capabilities with both domestic and international sales strategies and revenue targets. Support sales teams by ensuring operational readiness for client acquisition, pricing, proposals, and fulfilment across diverse global markets. Enable business growth by aligning supply chain, production capacity, and delivery timelines to meet the demands of domestic and export B2B clients . Ensure client satisfaction by meeting product specifications, timelines, and service level agreements (SLAs). Manage domestic and international logistics, including customs, documentation, and freight optimization. Implement ERP systems, manufacturing software, and automation tools to streamline operations and improve data visibility. Continuously identify inefficiencies and lead operational improvement projects. Ensure adherence to regulatory standards related to exports, trade, hallmarking, ethical sourcing, and workplace safety. Mitigate risks in production, logistics, and supply chain through proactive planning and systems. Lead and mentor cross-functional operational teams across production, QC, logistics, and procurement. Build a culture of accountability, efficiency, and continuous improvement. Key Skills 15-20 years of operational leadership experience in a B2B setting, preferably in the jewellery industry. Strong understanding of the end-to-end jewellery production and distribution process. Proven track record in scaling operations, managing large teams, and optimizing supply chains. Experience with ERP implementation and operations automation. Bachelor's degree in Operations, Engineering, Business Administration, or related field; MBA preferred. (ref:iimjobs.com) Show more Show less

CA FRESHER - LIFE INSURANCE Job Description DESIGNATION : SM POSITION GRADE : L4 DEPARTMENT : CPC-Channel Support SUB DEPARTMENT : Reinsurance REPORTING POSITION : SM DOTTED LINE MANAGEMENT LEVEL : L4 Objective Of The Role Ensure efficiency & accuracy in processing of Reinsurance Data. Identification & execution of various audit assignments for reducing risk at operations level. Key Responsibilities Weightage - QC /Audit of Data Shared with Reinsurer Diligently checking the accuracy of the data prepared to be shared with Reinsurer on time meeting quarter end deadlines Continuous co-ordination with Reinsurers, Actuaries and Accounts Team Control Reports Checking Daily Control reports for specific activities which help in reduction of manual & system risk at Operations level. Developing new reports and evaluating the feasibility of the same for enhancing team's efficiency & channelling the saved man-hours towards more appropriate value added activities. Audit Conducting various audits for plugging loopholes of different processes at user-end to reduce future operation losses. 50% 25% 25% TOTAL 100% INTERACTIONS Internal Relations : Operations, Accounts, Actuaries External Relations : Reinsurers Required Qualification And Skills Educational Qualifications : CA Work Experience : Insurance Ops or CA Audit Firm Other Skill Set Self-Managed Willing to take initiative Team-Worker (ref:iimjobs.com) Show more Show less

CA Fresher - Claim/Policy Servicing- Life Insurance Job Description This role is for SQA team Policy Servicing. SQA team conduct audits and QC activities of various processes within Policy Servicing, It also involves handling various external audits namely Internal audit of various processes and Statutory audit coordination. Key Deliverables Include Individual Contribution : Conducting various audits for plugging loopholes in different processes at the user-end to mitigate the risk of future operating losses/risks arising out of process gaps. Management Requirements Ensuring that the requirements (defined and ad hoc) sought by senior management are duly provided within time. Control Enhancement Developing new reports and evaluating the feasibility of the same for enhancing SQA's efficiency & channeling the saved man-hours towards more appropriate value-added activities. (ref:iimjobs.com) Show more Show less

I. Leadership And Team Management Supervision & Mentoring: Lead, guide, and supervise a team of Radiology Technicians across different shifts and modalities. Provide mentorship, conduct performance evaluations, and identify areas for professional development. Training & Development: Organize and conduct regular in-service training programs for junior technicians on new equipment, advanced imaging techniques, safety protocols, and patient care best practices. Workforce Planning: Prepare and manage duty rosters, allocate resources (technicians and equipment) efficiently to optimize workflow and minimize patient waiting times for various specialized investigations. Problem Resolution: Act as a primary point of contact for technical issues, patient concerns, or interpersonal conflicts within the radiology technician team, resolving them promptly and escalating complex matters to the Head of Department. Compliance: Ensure all team members adhere strictly to hospital policies, national/international standards (e.g., AERB guidelines, NABH, JCI), and best practices in radiology. II. Operational & Technical Excellence Advanced Imaging Procedures: Oversee and, if necessary, perform complex diagnostic imaging procedures across all modalities (X-ray, CT, MRI, Ultrasound, Mammography, DEXA, etc.) for various super specialties (e.g., Cardiac CT/MRI, Neuro MRI, Oncological imaging, Interventional Radiology procedures). Patient Preparation & Care: Ensure meticulous patient preparation, accurate positioning, and empathetic communication for all procedures, particularly for critically ill, pediatric, or non-cooperative patients. Equipment Management: Oversee the daily operation, quality control, and routine maintenance of all highly specialized radiology equipment. Coordinate with the Biomedical Engineering Department for preventive maintenance, calibration, troubleshooting, and repairs of imaging machines. Maintain detailed logs of equipment usage, service records, and any malfunctions. Evaluate new equipment and technologies, providing recommendations for procurement. Radiation Safety (for modalities involving ionizing radiation): Ensure strict adherence to ALARA (As Low As Reasonably Achievable) principles for radiation exposure for patients and staff. Monitor and manage radiation dose levels, ensuring compliance with AERB guidelines and hospital radiation safety protocols. Oversee the use of appropriate shielding and PPE. Conduct periodic radiation safety audits and drills. Image Quality & Diagnostics: Monitor and ensure consistent production of high-quality diagnostic images across all modalities. Implement and oversee quality assurance (QA) and quality control (QC) programs for imaging equipment and processes. Troubleshoot image quality issues and take corrective actions. Assist radiologists in complex cases, providing technical support and clarification on imaging acquisition parameters. Contrast Media Management: Oversee the safe preparation, handling, and administration of contrast media, ensuring proper patient screening for allergies and renal function, and managing adverse reactions according to protocol. III. Documentation & Quality Assurance Record Keeping: Ensure accurate and comprehensive documentation of all patient details, imaging parameters, contrast administration, radiation doses, and procedure notes in the Hospital Information System (HIS) and Picture Archiving and Communication System (PACS). Reporting: Generate periodic reports on departmental workload, equipment performance, quality metrics, and incident reports. Audits & Accreditation: Actively participate in internal and external audits (NABH, JCI, AERB) related to radiology services. Implement and monitor corrective and preventive actions. SOP Development: Contribute to the development, review, and updating of departmental policies, procedures, and Standard Operating Protocols (SOPs) in line with best practices and regulatory requirements. Incident Management: Promptly report and document any equipment failures, patient adverse events, or safety incidents, participating in root cause analysis and implementing corrective measures. IV. Collaboration And Communication Inter-departmental Coordination: Foster excellent communication and collaboration with radiologists, referring clinicians (surgeons, physicians, oncologists), nurses, IT, CSSD, and other hospital departments to ensure seamless patient care pathways. Patient & Family Communication: Effectively communicate with patients and their families, explaining procedures, addressing concerns, and providing reassurance in a compassionate manner. Job Identification 30030 Posting Date 06/01/2025, 09:19 AM Apply Before 06/15/2025, 09:19 AM Degree Level Diploma Job Schedule Full time Locations 127, Shankarsheth Rd, , Pune, Maharashtra, 411042, IN Show more Show less

Selected Intern's Day-to-day Responsibilities Include Create motion graphics and visual effects using Adobe After Effects. Support editors on commercial and branding video projects. Learn real-world workflows, teamwork, and QC standards used in agency-level production. About Company: DGC Edits is a professional video editing service provider dedicated to helping individuals and businesses bring their video projects to life. Show more Show less

Client Coordination: Handle communications with distributors, dealers, and corporate clients via phone, email, and WhatsApp. Maintain client databases and ensure timely follow-ups for orders, payments, and inquiries. Assist in preparing quotations, price lists, invoices, and customer service responses. Inventory & Stock Management: Coordinate daily with the storekeeper to track raw materials, packaging material, and finished goods. Maintain stock reports and notify management about shortages or excess inventory. Assist in planning stock dispatches and incoming materials with logistic coordination. Documentation & Reporting: Create and update price lists, product catalogs, and sales presentations. Maintain and organize files for purchase orders, bills, vendor details, and other important documents. Prepare daily/weekly/monthly reports for management on sales, inventory, and operations. Administrative Support: Assist in scheduling meetings, managing calendars, and organizing business travel (if any). Support in vendor communication for raw materials, print jobs, packaging suppliers, etc. Coordinate with internal departments like production, QC, accounts, and logistics as required.

We are looking for a proactive and detail-oriented Quality Control Engineer to join our flexographic plate-making team. While prior experience in the flexo printing industry is not mandatory, the candidate should have a solid understanding of quality control principles in a production or manufacturing environment. The selected individual will be trained in the flexo plate-making process and will be responsible for planning daily production and inspecting plates for defects during and after the production process. Key Responsibilities: Production Planning: Plan and coordinate daily production schedules for flexo plate manufacturing. Ensure optimal use of materials, machines, and manpower for timely and efficient output. Liaise with internal teams to prioritize jobs based on urgency and customer requirements. Quality Inspection & Control: Conduct visual and dimensional checks on flexo plates during and post-production to identify any defects or inconsistencies. Learn and apply key quality parameters specific to flexo plate making (training will be provided). Document quality issues and assist in implementing corrective actions. Monitoring & Process Support: Monitor the production process to ensure adherence to quality standards and SOPs. Report any process deviations or recurring issues to the supervisor. Support in developing and updating inspection protocols and checklists. Reporting & Documentation: Maintain QC logs and production reports. Provide feedback and improvement suggestions to enhance output quality and reduce rework. Requirements:Diploma or Degree in Mechanical, Printing, Industrial, or Production Engineering. 1–3 years of experience in a quality control or production planning role in any manufacturing or printing-related industry. Basic knowledge of quality systems, visual inspection methods, and reporting tools. Strong attention to detail, problem-solving ability, and commitment to quality. Willingness to learn flexo plate production and its quality standards. Good communication and coordination skills. Preferred (but not required):Exposure to printing, packaging, or plate-making industries. Familiarity with ISO standards or quality assurance tools such as 5S, Root Cause Analysis, etc.

Responsible for 100% Adherence in opening of hub at 6AM Receiving the load from vehicle to the hub & in the portal with the other TLs Sorting shipments according to Pincodes & Route wise in coordination with other TLs Negotiating with riders during allocation of shipments Ensuring 100% OFD of rider partners by 10AM & OFP- 2PM Bagging & Connecting the RTO, RTS Shipments & bags Updation of Pincode to be done for the misroute & non-serviceable zone shipments Tracking live performance of rider partner by viewing the statuses updated by the rider partner, solving on field queries & analyzing the dashboards Real time calling on Not Contactable, CID and non OTP canceled cases Closure of runsheet after completion of delivery & pickup rider wise Adherence of Secondary QC Check before closing pickup runsheet Ensure collection of Cash On Delivery amount from riders Mandatory adherence of Inventory Reconciliation on daily basis Maintaining the safety & hygiene of the rider partners

Having hands on experience in BIS testing 694 or 1293. 1–3 years of experience in quality control, quality assurance, or laboratory testing in a manufacturing or industrial setting. Hands-on experience with laboratory equipment calibration, testing procedures, and inspection documentation. Proficient in reading and interpreting technical drawings and quality standards (BIS, ISO, ASTM, IEC). Knowledge of Production Part Approval Process (PPAP). Familiarity with CAPA (Corrective and Preventive Action) processes and root cause analysis tools (e.g., Fishbone, 5 Whys). Ability to prepare inspection reports and maintain detailed quality documentation. candidate from Cable Industry will get preference.

Job Title: Quality Control Executive Location: Sanaswadi ,Pune Job Summary: The Quality Control Executive is responsible for monitoring, inspecting, and testing products or materials to ensure they meet specified standards. The role includes maintaining quality systems, ensuring compliance with regulations, and helping to drive continuous improvement in product quality. Key Responsibilities: Conduct routine and non-routine analysis of raw materials, in-process samples, (PVC panels.) Perform quality checks Ensure that products comply with quality standards Maintain documentation Identify quality issues Train and guide junior QC staff if required.

👷‍♂️ Hiring – Supervisor (Production | Lashkaraa, Surat)📍 Location: SKB Retail India Pvt. Ltd., Surat 🕘 Time: 10:00 AM – 7:00 PM | 📆 Sunday Off 💰 CTC: Based on experience Role & Responsibilities:Supervise daily work of tailoring, embroidery & QC staff Assign tasks and ensure timely output from workers Maintain daily work and production reports Coordinate with design and production heads for smooth flow Monitor discipline, attendance & productivity of floor staff Resolve any work-related issues on ground level Preferred Candidate Profile:Experience in handling 25–50+ workers on production floor Strong communication and basic reporting knowledge Background in textile/garment industry preferred Must be organized and team-oriented 📩 Apply with Resume to: 7778972940

Roles & Responsibilities: Responsible for 100% Adherence in opening of hub at 6AM Receiving the load from vehicle to the hub & in the portal with the other Sorting shipments according to Pincodes & Route wise in coordination Negotiating with riders during allocation of shipments Bagging & Connecting the RTO, RTS Shipments & bags Updation of Pincode to be done for the misroute & non-serviceable zone Tracking live performance of rider partner by viewing the statuses Real time calling on Not Contactable, CID and non OTP canceled cases Closure of runsheet after completion of delivery & pickup rider wise Adherence of Secondary QC Check before closing pickup runsheet Mandatory adherence of Inventory Reconciliation on daily basis shipments

Job Title: Senior Press Operator – Automobile Press Parts Manufacturing Company: Amit Engineering and Tools Pvt. Ltd. Location: Chakan, Pune Reporting To: Production Manager / Plant Head Job Summary: Amit Engineering and Tools Pvt. Ltd., a leading manufacturer in the automobile press parts industry, is seeking an experienced Press Operator with 5–6 years of hands-on experience in automotive sheet metal component manufacturing and production planning & control (PPC). The candidate will be responsible for press operations, quality adherence, and supporting the execution of production plans effectively and efficiently. Key Responsibilities: 1. Press Machine Operation: Operate mechanical and hydraulic press machines (progressive, tandem, single stage). Perform die setup and tooling changes as per production requirements. Conduct first piece inspection and ensure continuous quality compliance. Monitor machine parameters and attend to minor mechanical issues. 2. Production Planning & Control (PPC): Execute production plans in alignment with PPC schedules. Ensure timely availability of materials, manpower, and tools for uninterrupted production. Monitor and report daily outputs, downtime, and rejection rates. 3. Quality Assurance: Conduct in-process checks and ensure adherence to customer quality standards. Collaborate with QA/QC team on inspection procedures and documentation. Follow and promote 5S, Poka-yoke, and Kaizen practices for continual improvement. 4. Maintenance & Safety: Carry out basic preventive maintenance of press machines. Ensure all safety protocols are strictly followed. Participate in root cause analysis and implement corrective actions. 5. Documentation & Reporting: Maintain production records, machine logs, and rejection reports accurately. Provide shift handover reports and coordinate with cross-functional teams. Support internal and customer audits with required documentation. Key Skills & Competencies: In-depth knowledge of press operations, tooling, and sheet metal fabrication. Familiarity with automotive industry quality systems like IATF 16949. Practical exposure to lean manufacturing, 5S, and Poka-yoke. Ability to interpret technical drawings and production schedules. Working knowledge of ERP systems is an added advantage. Strong team coordination, time management, and problem-solving skills. Educational Qualifications: ITI / Diploma in Mechanical Engineering / Tool & Die / Production. Certifications in press tools or PPC systems are preferred. Experience: 5–6 years in automotive press part manufacturing and PPC in Tier 1 or Tier 2 supplier companies. Salary Range: Rs. 15,000 to Rs. 60,000 per month, depending upon skills, certifications, and experience.

JOB SUMMARY: We are seeking an experienced and detail-oriented Quality Control Engineer to lead and oversee quality assurance processes in our namkeen manufacturing facility. The ideal candidate will ensure product consistency, compliance with food safety standards, and continuous quality improvement in line with FSSAI and other relevant regulatory guidelines. KEY RESPONSIBILITIES: Quality Assurance & Compliance Develop, implement, and monitor quality control procedures to maintain high product standards. Ensure compliance with FSSAI, ISO 22000, HACCP, and GMP standards. Conduct regular audits (internal and external) and inspections of raw materials, production processes, and finished goods. Process Monitoring & Control Oversee in-process quality control at various stages of namkeen production (mixing, frying, seasoning, packaging). Monitor critical control points (CCPs) and preventive control measures. Team Leadership & Training Lead the QC team and coordinate with production, procurement, and R&D teams. Train staff on hygiene standards, quality practices, and SOP adherence. Documentation & Reporting Maintain and manage quality documentation including checklists, test reports, batch records, and deviation logs. Generate regular quality performance reports and recommend improvements. Root Cause Analysis & CAPA Investigate non-conformance or customer complaints; conduct root cause analysis and implement Corrective and Preventive Actions (CAPA). Product Development Support Work with R&D to validate new product trials and ensure quality parameters are met. QUALIFICATIONS AND SKILLS: Bachelor’s or Master’s degree in Food Technology, Food Science, Chemical Engineering, or a related field. 5 years of experience in quality control, preferably in the namkeen or snacks industries Strong knowledge of FSSAI, HACCP, ISO, and other relevant quality systems. Experience in managing audits and working with external regulatory bodies. Analytical mindset with a strong attention to detail. Proficiency in MS Office, quality management software/tools. Good leadership, communication, and team management skills.

Axalta has remained at the forefront of the coatings industry by continually investing in innovative solutions. We engineer technologies that protect customers’ products – whether they are battling heat, light, corrosion, abrasion, moisture, or chemicals – and add dimension and beauty with colourful finishes. We have a vast and ever-evolving portfolio of brands primed to play an important part in everything from modernizing infrastructure around the world to enabling the next generation of electric and autonomous vehicles. We are currently looking for a Production Officer to join us at our facility in Savli. Key responsibilities: Demonstrate Core Values of Axalta i.e. Safety, Ethics and Valuing people. To achieve Planned Production target to meet the Market Demand. To ensure quality of the product as per required specification. To ensure generation of Quality Incidence Report for observed process deviations and work in team to resolve the same with QC, Process Engineer and Technical, if required. To take active part and support for Quality Complaints resolution, doing RCFA and implement CA and PAs’. Plan and arrange Raw Materials and Packaging Materials as per Production Plan, and responsible for shop floor RM/PM accounting and variance. To implement ISO 9000 requirements on shop floor and ensure all record generation, maintenance and smooth retrieval. Reporting of incident of any nature as per the site SHE procedures. Co-ordinate with Maintenance team for improving the performance of the Plant. To ensure healthy 5 “S” for AXALTA Savli Unit Basic safety knowledge of plant operation. Basic Knowledge on weight measurement process in filling and packaging area. Basic Knowledge on MRP printing and label Printing. Require knowledge on Excel and word in computer. To have basic understandings of different Paint processing equipments. Must be familiar with SAP transactions. To have basic knowledge of HMI and SCADA operation The Candidate will be working in the rotational Shift Duty. Candidate Experience Required - 2-3 Years Qualification- BSC/MSC/BTech/BE- Production Industry- Chemical/Paint/Coating/ Ink Team handling or IC role- IC Reporting into- Section head Axalta operates its business in two segments: Performance Coatings and Mobility Coatings, which serve four end markets, including Refinish, Industrial, Light Vehicle and Commercial Vehicle, across North America, EMEA, Latin America and Asia-Pacific. Our diverse global footprint allows us to deliver solutions in over 140+ countries and coat 30 million vehicles per year. We’ve recently set an exciting 2040 carbon neutrality goal, in addition to 10 other sustainability initiatives, and we take pride in working with our customers to optimize their businesses and achieve their goals. Our Company: Axalta has remained at the forefront of the coatings industry by continually investing in innovative solutions. We engineer technologies that protect customers’ products – whether they are battling heat, light, corrosion, abrasion, moisture, or chemicals – and add dimension and beauty with colorful finishes. We have a vast and ever-evolving portfolio of brands primed to play an important part in everything from modernizing infrastructure around the world to enabling the next generation of electric and autonomous vehicles. Axalta operates its business in two segments: Performance Coatings and Mobility Coatings, which serve four end markets, including Refinish, Industrial, Light Vehicle and Commercial Vehicle, across North America, EMEA, Latin America and Asia-Pacific. Our diverse global footprint allows us to deliver solutions in over 140+ countries and coat 30 million vehicles per year. We’ve recently set an exciting 2040 carbon neutrality goal, in addition to 10 other sustainability initiatives, and we take pride in working with our customers to optimize their businesses and achieve their goals. Show more Show less

Company Description Auto Pickup Petro chem Pvt. Ltd. is a fast-growing manufacturer of high-quality engine oils and greases, established in 2020. The company, originally operating under Sri Niwas Lubricants since 2006, aims to offer premium lubricants for both automotive and industrial segments. Located in New Delhi, our state-of-the-art manufacturing plant ensures top-notch products, including gear oils, engine oils, coolants, and greases. We have a widespread distribution network across India, dedicated to delivering excellent products and services at affordable prices. Role Description This is a full-time on-site role for a Production Manager located in Bahadurgarh. The Production Manager will oversee daily production operations, ensure adherence to manufacturing standards, manage production schedules, and coordinate with various departments to optimize workflow. Responsibilities also include maintaining safety protocols, troubleshooting production issues, and striving for continuous improvement in production processes. Qualifications Strong Knowledge in Manufacturing Processes and Production Management Experience in Quality Control and Safety Standards Team Leadership and Management Skills Familiarity with Industrial Equipment and Maintenance Excellent Communication and Problem-Solving Skills Ability to work in a fast-paced environment and meet deadlines Bachelor's degree in Engineering, Manufacturing, or a related field Experience in the automotive or lubricant industry is a plus. Exact Job descriptions:- 🚀 We're Hiring: Production Manager – Lubricants Manufacturing 📍 Location: Bahadurgarh, Haryana (Manufacturing Plant) | 🏭 Industry: Lubricants | 💼 Experience: 3+ Years Are you ready to drive the heart of operations in one of the most dynamic sectors of manufacturing? If you're passionate about production, safety, and innovation — and love leading from the front — this is your opportunity to make a real impact in the lubricants industry. 🔧 What You'll Do – Key Responsibilities ✔️ Lead the end-to-end production process — from planning to packaging ✔️ Ensure daily/weekly/monthly production planning based on sales & inventory forecasts ✔️ Monitor blending, filling, and packaging lines for smooth operations ✔️ Optimize resource allocation — manpower, machinery, materials ✔️ Drive quality assurance in collaboration with QC teams ✔️ Enforce safety regulations and best practices across the plant ✔️ Lead and mentor a team of production operators, shift leads & technicians ✔️ Implement process improvements to enhance efficiency and reduce costs ✔️ Manage project execution — new plant setups, commissioning, upgrades ✔️ Generate and present production reports & KPIs to leadership 🎓 Who You Are – Qualifications & Skills 🔹 Bachelor's in Engineering – Mechanical / Chemical / Industrial 🔹 3+ years in production or plant management in lubricants or allied industry 🔹 Strong understanding of formulations, quality protocols, and compliance 🔹 Excellent leadership, planning, and communication skills 🔹 Hands-on experience with ERP systems (SAP preferred) and MS Office 💡 Why Join Us? At Auto Pickup Petrochem Pvt Ltd, we don’t just manufacture lubricants — we engineer excellence. Join a team where innovation meets execution, and every shift brings growth, teamwork, and results. 🚀 Apply Now & Power Up Your Career 📩 Send your resume to 9711289333 (Whatsapp Quick Response) 📞 Contact: Nikhil Sachdeva HR Manager 9711289333 🔗 Apply via LinkedIn Easy Apply or just DM "Interested" – we'll review your profile and get in touch. 👉 Make sure to follow & connect with us first for quicker response! . . . . . . . 📢 #HiringNow #ProductionManager #LubricantsIndustry #PlantOperations #ManufacturingJobs #JobsInLubricants #ChemicalEngineering #MechanicalEngineer #OperationsLeadership #QualityAndSafety #SAP #ProductionJobs #IndustrialJobs #TeamManagement #ProcessImprovement #JobOpening #ViralHiring #LinkedInJobs #ApplyNow Show more Show less

As the global leader in high-speed connectivity, Ciena is committed to a people-first approach. Our teams enjoy a culture focused on prioritizing a flexible work environment that empowers individual growth, well-being, and belonging. We’re a technology company that leads with our humanity—driving our business priorities alongside meaningful social, community, and societal impact. How You Will Contribute CIENA's Packet products portfolio comprises of a broad family of products for access and aggregation tiers of the network. Typically spanning from the Metro edge to the customer edge, these products provide Carrier Ethernet/MPLS/G.8032/TDM services in mobile backhaul, enterprise and residential domains. The Packet Software and Access R&D organization is responsible for delivering platform-independent Service Aware Operating System (SAOS), Access products and next-generation virtualized operating system to support Virtualized/SDN/NFV applications. Solution test automation engineers will be responsible for automation suite for platform-independent current and next-generation packet software encompassing the broad spectrum of CIENA's networking products. You will get an opportunity to innovate and influence new technologies that shape the future of Next Generation networks. The Must Haves Automate solution test plans to verify product capabilities Execution of automated regression suites and reporting test results with artifacts using Quality Center (QC) Work closely with engineers across teams to ensure quality for the features Build in-depth knowledge of product architecture and develop ability to root-cause issues Coordinate activities with North America test and development teams on a need basis FS and test plan / scripts review Detailed knowledge of Carrier Ethernet products and at ease to ramp up quickly on new technologies and concepts SME on two or more of the following domains: Carrier Ethernet, MPLS, G.8032, OAM (BFD, CFM, EOAM, AIS), BGP, ISIS, OSPF Required Skills Position requires proficient troubleshooting and problem-solving skills Team oriented; strong inter-personal skills and ability to understand customers’ needs, expectations and perspective Demonstrated ability to multitask on multiple projects Demonstrated communications skills, both verbal and written, to effectively communicate/collaborate with remote QA and Development teams Strong commitment to product excellence and quality Quickly comes up to speed in understanding of advanced concepts/methodology and contributes to improving and extending the impact and effectiveness of those concepts or new approaches to the current project Conducts knowledge sharing sessions (Critical): Moderate to complex topics, including smaller protocol or RFC related information, specific functional area presentations or methods of procedures. Topics not product related that may help enhance process or efficiency, such introduction to new tools for testers Required Experience BE / B.Tech. (EE/CS) Degree About 4-8 years of relevant experience in telecommunications, test and automation Hands-on Experience on at least 2 of the following Networking Protocols: Carrier Ethernet, MPLS, G.8032, OAM (BFD, CFM, EOAM, AIS), BGP, ISIS, OSPF Good experience in Python is must Experience with Ixia traffic generators Experience on IxNetwork is desirable Understanding of AI and ML is desirable Not ready to apply? Join our Talent Community to get relevant job alerts straight to your inbox. At Ciena, we are committed to building and fostering an environment in which our employees feel respected, valued, and heard. Ciena values the diversity of its workforce and respects its employees as individuals. We do not tolerate any form of discrimination. Ciena is an Equal Opportunity Employer, including disability and protected veteran status. If contacted in relation to a job opportunity, please advise Ciena of any accommodation measures you may require. Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Manager 2 Date: Jun 12, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Experience from major pharma industries in Non-oral Products: Topical product and transdermal product. Experience in end-to-end topical product development activities for generic product development ANDA (Cream, ointment, gel, solution, lotion, foam, patch etc.) as well as NDA 505(b)(2), 505(b)(1). Experience in execution of lab scale manufacturing, reverse engineering, analytical know-how, plant level manufacturing activities; scale-up and exhibit batches based on quality principles QbD, QTPP, CQA, CMA, CPP, RA, FMEA. Experienced scientist to perform experiments for development of optimum prototypes (generic, non-infringing composition and robust manufacturing process) with diverse class of drugs & prodrugs (sensitive to pH, acid, base, temperature, oxygen, humidity). Experience in regulatory documentation CMC, MF, BMR, PDR, controlled correspondence for CMC, Biowaiver & Dossier preparation for US-FDA, EU-EMA, AU-TGA & DCGI through successful filing. Experience in working with cross-functional teams (ADD, MSTG, production, QC, QA, RA, IPC, PMO, BD, Microbiology, Pharmacology etc.) to achieve project goals - Filings and subsequent approvals. Knowledge and develop continuous understanding on competitive intelligence, due diligence, US-FDA quality concepts, statistics and global pharma trend analysis to support new product evaluation & introduction. Job Responsibilities: To design, conduct and verify/review experiments to develop a robust formulation. To do literature search, patent search, prepare summary report and review. To prepare product development reports and protocols. To do product scale-up, exhibit batches and prepare reports for product filing and regulatory queries including post filling and post approval market queries. To prepare documents (i.e. PDR, CPD etc.) for regulatory submission Group work co-ordination. Project status report preparation. Experimental result review, interpretation and conclusion. To prepare technology transfer documents. To procure raw materials (API / excipients), packaging materials, innovator samples in consultation with packaging/purchase department. To do product validation, site transfer/change activities of products. To write Laboratory Notebook to enter details related to drug product manufacturing. To prepare test request for analysis of raw materials (API/Excipients) and Drug product. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Background Praan (Praan, Inc.) is an impact focused deep-tech startup democratizing clean air using breakthrough filterless technology. The company is backed by top tier VCs and CXOs globally and currently operates between the United States and India. Our team puts extreme attention to detail and loves building technology that's aspirational. Praan's team and culture is positioned to empower people to solve large global problems at an accelerated pace. Why Everyone worries about the dooms-day in climate change which is expected to occur in the 2050s. However, there's one doom's day which is the reality for millions of people around the world today. Air pollution takes more than 7 Million lives globally every single year. Over 5% of premature children death occur due to air pollution in developing countries. Everyone has relied on governments or experts to solve the problem, but most solutions up until today have either been too expensive or too ineffective. Praan is an attempt at making the future cleaner, healthier, and safer for the generations to come. Job Description Work on Quality Control for NPD as well as batch production parts made in steel, aluminium, FR4, and other materials. Ensure appropriate dimensionality, finish, safety, and fitment metrics required for each part at vendor sites prior to part dispatches to Praan Prepare quality planning documents for inspection across all vendor sites Audit the QC Process done by the supplier and their teams Improve Quality planning activities based on product and finish requirements Maintain MIS through dashboards for the daily QC checks for the parts and their fitment Overlook QC for finished products prior to dispatch and establish SOPs for current and upcoming products and accessories Work on action plan for non-adherence of targets Be pro-active by planning for available resources required for production and inspection cycles. Visit vendor sites to ensure quality consistency across raw material, process, finishing, and dispatch of goods to our production line Develop and implement procedures and checks based on audit policies to ensure adherence to quality standards and regulatory requirements Investigate and resolve quality-related customer issues by identifying root causes, implementing corrective actions, and monitoring for recurrence to enhance product reliability and customer satisfaction Coordinate and expedite purchase orders to ensure timely procurement and delivery of materials Oversee the acquisition and maintenance of required certifications ensuring all processes and products meet industry standards and regulatory requirements Collaborate closely with industrial design, mechanical engineering, and supply chain teams to ensure quality consistency without change in delivery timelines or dispatch Skill Requirements BS/MS in Mechanical, Production or relevant Engineering degree. 4+ years of experience as a NPD QA/QC Manufacturing Engineer Strong understanding of tolerances and finishes. Past experience and understanding of manual and computer-automated manufacturing processes Past experience drafting and following QA/QC Manufacturing processes Excellent Communication Skills Good to Have CAD/File review and edit experience Past experience working at a startup Praan is an equal opportunity employer and does not discriminate based on race, religion, caste, gender, disability or any other criteria. We just care about working with great human beings! Show more Show less

Our Team Sanofi Business Operations is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. Sanofi Business Operations strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally. Main Responsibilities The Associate Statistical Programmer will work with Medical Affairs biostatisticians and/or programmers and Sanofi Business Operations biostatistics and programming personnel to implement statistical analysis plans and provide QC’d data packages including tables, figures, and listings for use in publications (i.e. abstracts, posters, oral, presentations, manuscripts, and ad-hoc data analysis requests) ; The Associate Statistical Programmer will assist in developing, implementing of programming techniques. The Associate Statistical Programmer will ensure SOPs are followed and that timelines and quality standards are met. People: 1) Develop and maintain effective relationships and collaborations with the end stakeholders (Medical community) and local biostatistics and/or programming team members within the allocated Global business unit and product – with an objective to develop statistical data outputs. Performance / Process: 1) Conduct appropriate post-hoc statistical analyses of clinical trial data and/or registry. 2) Design, develop, test, implement, and document statistical programming in high-level software packages e.g. SAS. 3) Produce well documented data packages that include tables, listings, and figures. 4) Closely follow QC plans and timelines set by senior members of the Sanofi Business Operations biostatistics and programming team. 5) Remain current on advanced programming methods Customer: 1) Work closely with Global Medical Affairs biostatisticians and/or programmers to identify statistical analysis needs and assist in developing assigned deliverables. About You Experience: B.Sc. or Master's degree minimum 1 years of relevant experience required, or a minimum of 6 months of relevant internship experience. Soft skills: Ability to manage timelines and Ability to work independently and within a team environment. Technical skills: Base SAS programming skills, basic knowledge SDTM & ADaM (CDISC) Education: Bachelor or Master of Science degree or equivalent in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related field. Languages: Excellent English language knowledge – written and spoken Pursue progress, discover extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com! null Show more Show less

Technology Architect is responsible for programming and delivering solutions for products which have been continuously evolving to meet clients requirements. Day to day activities involve clear understanding of business requirements, bug fixes, doing impact analysis, implementing and documenting the right solution. It also involves close coordination with all stakeholders like BAs, Product Management, QC and Support teams. Responsibilities Troubleshoot and debug applications. Learn about new technologies. Stay up to date with current best practices. Manage cutting- edge technologies to improve applications. Collaborate with multidisciplinary team of designers, developers and system administrators. Be involved and participate in the overall application lifecycle. Focus on coding and debugging. Help and support to other team members. Build high- quality reusable code that can be used in the future. Develop functional and sustainable web applications with clean codes. Show more Show less

Adv Engineer: Skid Engineering / Piping Layout: JD: DIRECTLY ACCOUNTABLE for: • Preparation of Basic/Detailed engineering deliverables consisting of Plot Plan, Equipment GA, Piping Layout, Pipe Rack Study Sketches, Vessel Nozzle Orientation, Vent and Drain Piping Layout, Process and Utility Piping Design Drawing, Line List, Critical Line List, Skid Fabrication & transportation documents while ensuring compliance to UOP's technical specification, Process and Procedures. • Incorporating the requirements of Local/statutory Requirements viz factory inspector, Oil Industry Safety Directorate(OISD), Indian Boiler Regulation(IBR), chief controller explosives(CCoE/PESO), tariff advisory committee (TAC), pollution board, local bodies, aviation authorities, and should have good knowledge of hazardous area classification. • Studying and appraising applicable codes on a Project, standards & statutory regulations, Site design data including facilities around the plot. • Providing inputs to Structural, Static, Rotary, electrical / instrumentation groups for various purposes. • Providing Guidance and review of 3D software (e.g. PDS, PDMS, Plant 3D etc.) database set-up by Detailed Engineering Contractor (DEC) at the beginning of Project. • Inspection and testing of piping skids/ modules during fabrication/ construction for conformance with project equipment requirements and applicable codes. • Routing of Stress Critical line. Shall be well versed with Piping Stress, Piping Material and Different Specialties. • Providing inputs to procurement process consisting of preparation of material/ purchase requisitions (for bids, for ordering, for costing exercises, design specific QA/ QC requirements etc); conducting evaluation of vendor bids including liquidating of TQ's etc; conducting review of vendor engineering deliverables (like data sheets, drawings etc). • Meeting expectations for delivering sales support and on-site technical services to customers for existing units etc. • Preparing/ reviewing and/ or approving following documents either created by in-house engineering team or by a team from third party agencies: Ø General Arrangement and Piping Layout within the Skid or within the Module including pipe supports to allow for safe operation and maintainability consistent with Industry standard and practices. Ø Piping isometric drawings along with the Bill of Material consistent with piping layout. • Candidate should have thorough knowledge of 3D software and Responsible for leading 3D modelling effort and reviews using SPR, Navisworks software or some other similar software. • Reviewing the work of others in the group for technical accuracy and compliance with established guidelines and procedures and be the approver for all piping related deliverables. • Ensuring to meet customer satisfaction requirements, including UOP Quality standards and UOP technical standards. • Actively participating to ensure that ISO 9001 certification is maintained. • Providing input and participating in vendor performance evaluation reviews, project close-out reports and subsequent meetings. Acting on applicable specialist group-related RCA's (root cause analysis) for CAPA's (corrective & preventive actions) that come out of these reviews. • Following-up on items and lessons learned for applicable specialisation as captured thro' RCA's for a CAPA, field reports, establishing root cause and implementing corrective actions. • Providing deliverables within budgeted cost and schedule at a high level of quality • Communicating with project manager on a regular basis regarding progress, changes & schedule. • Keeping up to date with current technology developments in area of expertise and sharing this knowledge with others, where appropriate through leadership of Community of Practices. • Managing applicable specialist group-related documentation and working with the Team to implement the Document Management system to ensure alignment with work process. • Supporting and following corporate HS&E policies, in relation to Office & Field Safety practices and engineering design policies. Additional Position Accountabilities include: • Identifies needs and opportunities for Work Process and Productivity improvements (in area of expertise) and provides necessary oversight through implementation • Sets technical standards, policies, and procedures in area of expertise • Coordinate revisions and improvements going forward • Supports the Manager for development and maintenance of outside supplier relationships, as assigned • Explains UOP's philosophy regarding equipment issues to internal and external customers • Represents area of expertise on UOP equipment teams, as assigned Minimum Required Competencies : • Relevant 8+ years of experience in detailed engineering Skid Engineering &/or Piping Layout discipline for the petroleum refining & petrochemical industry. • Candidate shall have an excellent knowledge of Principles, Practices and Procedures related to piping engineering. • Excellent knowledge of B31.3 Piping Code. • Expertise in Plot Plan, General Arrangement, Skid Engineering and Piping Layout within the Skid or within the Module including pipe supports. • Candidate shall have knowledge and competency with 3D modeling. • Review of piping isometric drawings along with the Bill of Material consistent with piping layout. • Has prior experience of design and analyzing piping systems. • Experience/ Knowledge of inter-disciplinary linkages & interdependencies. • Understanding of Equipment Design and Fabrication techniques, standards and tools. • Excellent interpersonal and communication skills to be used at the international level with colleagues worldwide. BASIC QUALIFICATIONS: • Minimum bachelor's degree in mechanical. • Master's degree may be an asset. • Able to communicate effectively in English. ADDITIONAL QUALIFICATIONS: • Good analytical skills and sound judgment. • Highly motivated, Independent and Team player • Negotiation skills and business acumen are an advantage Show more Show less

Job Purpose To assess the quality of Billets from time to time to ensure right quality received from the supplier. To develop a quality culture through continual improvements and team working. Analyze reasons for external and internal and initiate, monitor and implement corrective actions, to prevent recurrence Ensure guidelines are followed in the case of products where special testing is required to satisfy the customer Liaison with external agencies for third party inspections. Initiate action plans to reduce customer complaints, sales return and internal rejection. Identify and train employees on any special needs identified for effective working of the systems to develop the right competencies. Monitoring of the KPI’s on monthly basis & initiating the plans to achieve to meet the requirements. Visit to Customers for understanding customer perceptions Understand Customer process and applications. Provide inputs for developing customer specific practices. Develop/modify products based on customer inputs. Lead Quality control subcommittee, Deployment of QC tools. Implementation of Quality control projects. Carry out RCA (5 why, fish bone, 8D) Have an advanced understanding of product, process and system standards and requirements relevant to aluminium extrusion Show more Show less

Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait . We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. Job Description QC and formatting of clinical trial protocols, informed consent forms (ICFs), clinical study reports (CSRs), investigator’s brochures (IBs), and clinical data summaries for phase 1-phase 3 and post-marketing surveillance studies and as per agreed timelines. QC and formatting of clinical modules of eCTD dossiers for global approval in developed and emerging markets with high quality and as per agreed timelines. Ad-hoc writing support for clinical documents such a ICFs, CSRs and protocols CSR publishing for regulatory submissions. Ad hoc QC and formatting support for cross-functional teams in Medical Affairs and Clinical Development Support in creating and/or updating SOPs, checklists, and templates. Work collaboratively with other medical writers and cross-functional stakeholders within the Clinical Development function. Support Group Lead in maintaining and tracking medical writer occupancy and resourcing Qualifications M Pharm with minimum 5 years of experience in document QC and formatting within the pharmaceutical industry Excellent written, spoken, interpersonal and presentation skills Proficiency in editing and formatting documents using Microsoft Office and Acrobat. Good understanding of medical terms, clinical trials, and drug development process. Ability to analyze and interpret scientific and medical data Highly detailed orientated and excellent time management skills Additional Information About the Department Biologics Currently operates in the Global Biosimilars business - a segment that is poised for attractive and sustained growth over the next 10–15-year time horizon. With a robust portfolio of biosimilar products across key therapeutic areas, covering ~US$80+ Bn in innovator sales – future business pipeline covers a variety of product classes and therapy areas, and new modalities. Fully integrated organization with over two decades of experience in developing, manufacturing and commercializing multiple biosimilar products. With a Product Development engine that has end-to-end capabilities – in-house clone development, upstream and downstream process development, bioanalytical development and proprietary formulation. Supported by a Clinical and Regulatory team with experience in executing complex biosimilar programs with innovative global trial designs. We have a proven experience in commercial-scale manufacturing across a variety of technology platforms with global quality standards and a highly competitive cost structure Rich experience of commercializing high-quality biosimilars in multiple markets with over 900,000 patients having benefited from our products till date. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/ Show more Show less

Purpose of the Role Within the framework Project vehicle or Program vehicle and Capacity enhancement - Ensures the processing and the industrialization Vehicle Production Process Engineering for the perimeter CMON in accordance with the EOL tool programming - Need to co-oridnate with enginnering team to understand the requirements and carry the advanceed study of EOL test requirment - Create EOL test Sequnce creation and standarsing EOL Process sheet, Station readiness and drive the issues . - Interface with the other department(Project, Quality, Manufacturing, Product) Job Responsibilities - Advanced study during co design phase. - Raise Manufacturing issue in PLM & follow up for resolution with Product - Write the technical requirements to be met by the product to allow the industrialization of the chosen solution - EOL Test sequence creation for diffenet station ( Flashing , Brake filling, Rolls & Brake, Wheel Alignemnet ,ADAS,Final check ) production tools - Incorporating the new model vehcile in Filling machine, wheel alignmnet , Rolls & Brake , ADAS - Anaylse the DTC with avaialble infomration and drive the Engineering team for solution. - Anayse the CAN logs using different tools and conclude the issue for NRC. -Tooling, Jigs, Fixture Design & Implementation for EOL Process - Process FMEA, control plan creation for Critical/Safety process - Keep a detailed inventory of the EOL process in the various terminal factories. Identify deviations from the repository and propose convergence actions - Assisting the team in case of any technical failures/breakdown to troubleshoot and to rectify issues at the earliest - Equipment Technical Specification creation, RFQ creation, Technical Alignment , Installation , Snag Closure & Buy off. - Supplier Selection, Technical Specification creation, Installation & Buy off. - Handover to Serial life Production - Lesson learnt creation & Feed back to Upcoming New vehicle models - Repair process creation for New Vehicle. Job Specification Qualification Engineering Graduate Experience 5 ~ 10 years Experience Competencies a) Technical Assembly Layout & architecture Knowledge in CANoe,Canalyzser Java,CMD,MS office Knowledge in Vehicle Architecture , UDS protocol FMEA, A3 Resolution /8D/QC story approach in the Problem Solving b) Behavioural Good Communication in English , French /German is added advantage Good Negotiator Proactive Approach Capacity with decision making , Prioritization Show more Show less