634 Raw Material Jobs - Page 4

Source and evaluate suppliers and materials Manage purchase orders, quotations, and vendor negotiations Collaborate with the accounts and production teams for seamless operations Maintain proper documentation for procurement activities Required Candidate profile Graduate in Commerce, Business, or related field [Mechanical Preferable] Minimum 1 year of relevant experience (Freshers with strong skills can apply) Proficiency in MS Excel, Tally or ERP systems

We do have urgent requirement for "Die Casting" Company. Designation: Store manager Qualification: Any graduate Location: Bhosari, Pune Must knowledge required in store department Contact no Mr. Prasad 73870 80121

Job Title: QMS Coordinator Job Location: Syngene International Limited, Bengaluru About Syngene : Syngene ( www. syngeneintl. com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Core Purpose of the Role: This is an exciting opportunity to play a pivotal role in driving quality excellence at Syngene through the QMS function. The role offers exposure to implementing cutting-edge quality practices and refining compliance workflows, ensuring operational efficiency and regulatory readiness. It provides a platform to proactively identify improvement areas, embed quality culture across functions, and stay ahead of evolving standards in Formulations. Role Accountabilities: Drive the continuous enhancement of Syngene s Quality Management System by developing robust, in-house processes that reduce dependency on external audits and consultants. Begin by performing an in-depth review of existing QMS frameworks and regulatory guidelines. Design and implement optimized quality workflows leveraging digital tools and risk-based thinking. Evaluate system effectiveness through CAPA trends, and compliance metrics to identify process improvement hotspots. Based on these insights, the QMS evolved to support readiness for global regulatory expectations. Syngene Values: All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience Demonstrated Capability Education Experience: Candidate should have 9 -12 years exposure in Oral Solid Dosage forms and injectable facility quality assurance activities. Candidate should have USFDA audit exposure. Establish good Interpersonal skills with cross-functional teams. Skills and Capabilities: Expertise in handling multiple expression platforms Capable of thinking scientifically to address complex problems and develop solutions Work as a team and have collaborative mindset Good communication skills Education: B. Pharm/ M. Pharm Job Description: Key Responsibilities: Create/ revise procedures and other related documents as applicable. Review of SOPs, IOPs, EOPs, Protocol and Reports for Formulation Facilities. Handling of Change Controls, Deviations, CAPA, Customer complaints, Self-Inspection and Internal Quality Audit. Perform Trending of Change Controls, Deviations, CAPA, LIR and Customer complaints. Ensure compliance with observations of Self Inspection, Internal Quality Audit and client or regulatory audit. Perform activities related to SAP. Vendor qualification of raw material, packing material, consumables, contractors engaged in manufacturing pertaining to GMP manufacturing with respect to vendor questionnaire verification, vendor audit and compliance report verification for approval. Approval of vendors by desktop and site audits. (As required) Review of Risk assessment document from the vendor. Verification of vendor rating documents from the purchase. Inspection of RM, PM and consumables for any damage and discrepancy possible during receipt, storage dispensing and handling of these materials in warehouse. Review of vendor Quality Agreement. Preparation and updation of requalification schedule for Manufacturers. Archival of documents. Issuance of annexures and logbooks. Provide data for QMR and QGF meeting. Provide line clearance to Dispensing, Manufacturing and Packaging area. Provide dispatch clearance for Shipment. Preparation & Review of RSG report. Review and Approval of Calibration Certificate. Review of executed BMR and BPR. Responsible for review and release of Batches. Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

JD FOR OLIGO PRD Designation : Purification Scientist Job Location: Bangalore Department : Chemical Development - Oligonucleotide About Syngene At Syngene, Safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and sops, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards always Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Job Purpose: The key objective of the role is to support the oligonucleotide development activity in a PRD facility at Syngene. The candidate is expected to generate engineering data in the laboratory and provide technical inputs and hands on support to ongoing projects, based on thorough literature information or evaluation of available experimental data. Having good knowledge in the documentation like, Technology transfer document, risk assessment, and Investigation report. Knowledge of optimization and scale-up of anion exchange chromatography and ultrafiltration is essential. Support for the manufacturing activity. Having previous oligonucleotide/peptide synthesis knowledge is a plus. Key Responsibilities: Purification of MAbs, Peptides, Oligonucleotide and ADCs Experience with AKTA Systems: AKTA Pure, AKTA Pilot, and AKTA Bioprocess, AKTA Process & also worked with Continuous Chromatography. Support R&D for the development of the processes feasible to execute at the manufacturing facility. Perform a chromatography and ultrafiltration processes for the development activity. Maintain the raw material inventory and instrument spare part inventory. Interpretation and compilation of analytical data. Follow environment, health, and safety (EHS) requirements always in the workplace ensuring individual and lab/plant safety. Support manufacturing team at all stages of the execution of Oligonucleotide batches, this involves Synthesis, C & D process, Chromatography, Ultrafiltration, lyophilization and other daily activities. Follow up with Cross functional teams to complete the activities. Adhere to the Safety, Quality, Data Integrity norms as per policy. Prepare project related documents like, Process development report, Technology Transfer Document and weekly updates. Educational Qualification: M. Sc. , Biochemistry/Chemistry Technical/functional Skills: Experience in working in a Peptide/Oligonucleotide/ Biological upstream/downstream laboratory. Experience in setting up experiments and generate data suitable for technology transfer and execution at large scale. Experience in handling the automated instruments. Basic understanding of organic chemistry reaction principles. Basic understanding and knowledge on ion exchange chromatography, column purification and membrane filtration. Experience: 5-8 years post qualification Behavioural Skills: Should have the capability to work in a team and ability to handle demonstrate a good team spirit. While possessing a good ability to follow instruction should also demonstrate innovative in his/her approach, good communication skills. Should be proactive while working on allotted responsibility. Flexibility to work on shifts and staggered weekends depending on work responsibility. Equal Opportunity Employer: .

Role & responsibilities Handle all purchase-related tasks for mainly head office and schools, colleges, hostels including stationery, furniture, IT equipment, maintenance supplies, etc. Develop and maintain vendor relationships for regular supplies and services. Negotiate and manage Annual Maintenance Contracts (AMC) with service providers. Coordinate and communicate effectively with all units/branches regarding purchase needs and delivery status. Maintain records of purchases, quotations, invoices, and inventory. Ensure timely procurement as per requirement without delay. Assist in general administrative work at the head office. Ready to take up any task assigned by management (multi-tasking attitude). Ensure cost-effective and quality procurement through comparison and negotiation. Preferred candidate profile Graduate in any discipline (Commerce/Management preferred). Minimum 3-5 years of experience in purchasing/procurement/admin work. Strong computer skills MS Office (Word, Excel, Email), and Google Workspace. Excellent communication skills – written and spoken English, Marathi, and Hindi. Ability to coordinate across departments and vendors. Should be sincere, trustworthy, and willing to take initiative. Familiarity with basic accounting or ERP systems is an added advantage.

Job Summary We are seeking an associate for the Quality Control team responsible for conducting investigations in case of any failure, incidents, market complaint, OOS & OOT. The role involves ensuring accuracy in investigation, technical report writing/documentation, adherence to safety procedures and reporting discrepancies. Roles & Responsibilities • You will be responsible for conducting investigations in case of any failure, incidents, market complaint, OOS & OOT. The role involves ensuring accuracy in investigation, technical report writing/documentation, adherence to safety procedures and reporting discrepancies. • You will ensure accuracy of the documentation before submitting it for the Group Leader’s review or uploading online. • You will adhere to safety precautions and procedures during analysis. • Lab safety, following JSA (Job Safety Analysis), and using proper PPE (Personal Protection Equipment) at the workplace are emphasized. Qualification Educational qualification: A Bachelor’s degree in Chemistry, Analytical Chemistry, or a related field Minimum work experience : 5 to 7 years of experience in a laboratory setting, preferably in the pharmaceutical or related industry Skills & attributes: Technical Skills • Proficient in various analytical techniques, including sampling and analysis of packaging and raw material samples. • Experience with the operation and maintenance of analytical instruments, ensuring proper use and care as per SOPs. • Competent in SAP activities related to sample tracking, documentation, and data entry. • Knowledgeable about cGMP, SOPs, and STPs, ensuring accurate documentation and adherence to specifications. • Adheres to safety precautions and procedures during analysis, emphasizing the importance of lab safety, JSA (Job Safety Analysis), and proper use of PPE (Personal Protective Equipment). • Expertise in handling and upkeep of the chemical and solvent store, including the preparation and maintenance of volumetric solutions and reagents. Behavioural Skills • Keen attention to detail in analysis and documentation, ensuring accuracy in all tasks. • Effective communication and collaboration skills for communicating with the Group Leader, reporting discrepancies, incidents, and providing timely updates. • Takes initiative in ensuring the proper use and care of instruments, timely destruction of samples, and other assigned responsibilities. • Demonstrates problem-solving skills in addressing discrepancies, incidents, and ensuring smooth laboratory operations. • Upholds ethical standards, compliance with SOPs, and follows regulatory requirements in all activities. Additional Information About the Department Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future. 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/#!/

Experience : Minimum 3 -4years Preferable in Solar Industry Qualification : Any Graduate Job Description : The role involves overall operation under factory shed of the production facility including overseeing all factory functions and daily management of factory staff. The role will demand competence both in technical and management capabilities, with the candidate expected to have a grip on core manufacturing functions and staff management. Production Planning, Scheduling Raw Material Planning Handling Production, Quality, Process, PPC, Maintenance, Dispatch logistics, stored under one roof. Identify manufacturing defects, improve process to minimize such defects.

Oversee receipt, inspection, storage, and documentation of lead scrap and other raw materials. Manage store systems ensure stock accuracy, and implement stock control mechanisms Ensure hazardous material handling compliance and safe disposal of waste Required Candidate profile Graduate in Science /Commerce / Engineering +Certification in Materials Management / SCM (preferred) Min 10 + year in similar roles preferably in metallurgical or lead-based manufacturing industries

" Job Title: Head Procurement - Raw Materials (DGM/ GM) Location: Mumbai Reporting to: Commercial Head About the client: PSS has been mandated to hire the Head of Procurement - Raw Materials for a well-established and highly reputed Indian pharma company manufacturing formulations OSD and Injectables. Key Responsibilities: Department: Procurement Raw Materials Location: Mumbai HO Reporting to: Commercial Head Job Responsibilities: Overseeing the sourcing and procurement of Raw Materials for the manufacturing plants. Identifying, evaluating, and developing new vendors by inviting quotations, negotiating, and pricing. Preparing comparison statements, obtaining the necessary approvals, and processing the orders. Obtaining all supportive regulatory documents for filing drug dossiers. Follow up with vendors for dispatch details. Follow up with the Logistics team / CHA for clearance of the material. Preparing the raw material cost estimations for projects based on the requirement. You will be responsible for Vendor development, Vendor Audit, and Ongoing Vendor Management, meeting Quality, Food Safety, and other regulatory requirements of the industry. You will ensure procurement of Quality & quantity on time with a focus on Cost optimization and savings. Educational Qualifications and Experience: MBA in Operations/ Supply Chain with 15 years of work experience in the Procurement of Raw Materials in the Pharma industry. Good understanding of procurement processes in a manufacturing setup, commercial acumen, ability to negotiate, supply chain. Ability to manage internal and external stakeholders of the company. #LI-NV1 ",

Job Title: Assistant / Deputy Engineer - Quality Job Description: We are looking for a Quality Engineer Incoming Inspection with a strong understanding of raw material inspection in the plastics industry. The candidate should be capable of handling instruments and communicating effectively with suppliers to ensure quality compliance. Key Responsibilities: Perform incoming inspection for raw materials (plastics). Operate and analyze using instruments like MFI, Moisture Analyser, Muffle Furnace . Ensure proper handling and control of inspection instruments. Generate and escalate NCRs (Non-Conformance Reports) to suppliers. Track and follow up on corrective actions from suppliers. Communicate monthly PPM (Parts Per Million) performance to suppliers. Use VMS (Vendor Management Systems) for supplier quality data management. Identify and document plastic defects and coordinate resolution. Must-Have Skills: Incoming Inspection Instrument Control Supplier Quality Presentation Skills Industry Knowledge: Plastic Raw Materials Plastic Defect Analysis Quality Documentation

1) Analysis of raw material, Drug substance (API), Intermediates, by HPLC, GC, GC-MS, LC-MS, NMR, FT-NIR, UV-Visible Spectrophotometer Instruments. 2) Analytical method development for raw material and finished products (drug products) by HPLC, GC, GC-MS, LC-MS, NMR, FT-NIR, UV-Visible Spectrophotometer, Dissolution Instruments. 3) Preparation and maintenance of volumetric solutions, buffers, etc 4) Calibration of laboratory Instrument like UV-Visible Spectrophotometer, Balances, pH meter, KF Titrator, etc., as per calibration schedule 5) Experience in chemical analysis like, titration, moisture, LOD, sulphated ash, TLC IR, SOR, Clarity of solutions and quantitative solubility tests 6) Exposure of GMP / GLP / GDP in laboratory. 7) Knowledge of separation techniques in chemical separation in chromatography in Normal and reversed phase systems 8) Preparation of Standard operating procedures (SOP) for all the instruments, equipment and procedures. 9) Qualification of instruments

Reviewing and organizing raw footage, including audio, video, and images Assembling raw material into a seamless and coherent finished product, using editing software such as Adobe Premiere Pro or Final Cut Pro. Cutting and splicing footage to create a smooth flow and pacing, and incorporating special effects, music, and sound effects as needed. Collaborating with the stakeholder or team to understand their creative vision and making suggestions for how to achieve it best. Ensuring that all technical specifications, such as aspect ratios, resolutions, and color correction, are met and that the final product meets quality standards. Staying current with new technologies and trends in video editing, and continuously improving editing skills and knowledge. Maintaining accurate records of all projects and assets, including backup and archiving. Excellent technical skills in video editing, including proficiency in non-linear editing, color correction, and special effects. Excellent creativity, storytelling, and storytelling skills, including the ability to turn raw footage into a compelling finished product. Strong attention to detail, including the ability to identify and correct technical and creative issues in the editing process Requirements Bachelor degree in Film Production, Media Studies, Marketing, or a related field. Proven experience in video production and editing, with a minimum of 3 years in a leadership role. Proficiency in video editing software (e.g., Adobe Premiere Pro, Final Cut Pro). Strong understanding of video production techniques, storytelling, and visual aesthetics. Excellent communication and interpersonal skills.\u200b Benefits Flexible working hours 5 Days working culture Health Insurance Benefits Tenure Recognition and Awards Leave Benefits as per Milestones Performance Linked Growth Opportunities Out of Term Appraisals

Is an urgent position. Revert on- sv22@svmanagement.com Responsible to maintain purchase cost saving dashboard. Costing of outsource part with supplier & settled costing norms New supplier development with norms finalization. New BOC parts price finalization. Totals spend analysis (RM and BOC) RM movements, amendments & provisions. Understanding of RM grades viz. flat steel and tubes Dealing with steel mills viz. Posco, Tata Steel, JSW Steel Responsible to maintain document records like -- NDA, Supplier tooling agreement, Supplier purchase and quality agreements. Monthly MIS Report Periodic supplier audit for improvements Candidate- BE / Diploma Engineer with 5-10 years of experience in automotive industry typically sheet metal company

Maintain, upkeep and execute processes of stores with regard to direct/indirect material, area of work, material handling equipment and storage etc. as per safety compliance, cGMP norms and QMS to support, execute and coordinate in functioning of stores processes. Key Accountabilities (1/6) Execute the store operations like receipt, dispensing and dispatch etc. materials as per cGMP procedure to avoid any cross contamination & to achieve manufacturing targets Execute the dispensing activities as per the plan Weigh, count and verify materials as per purchase order and receipt documents and store materials in designated area Manage the dispensing activity to ensure compliance to cGMP Dispense the materials required for manufacturing, stock transfer and exports as per cGMP norms Ensure cross contamination of material is prevented while handling by following all procedure strictly Key Accountabilities (2/6) Maintain the online documentation & area as per cGMP guidelines and regulatory requirements to avoid any deviation Review the status labelling of materials to ensure correct labelling is performed by quality Perform status labelling for equipment and accessories Monitor logs and area on day-to-day basis to avoid any deviation during internal and external inspection Update data entries in online documentation to avoid data integrity Key Accountabilities (3/6) Dispose the scrap generated periodically in stores to remove blockage and ensure smooth store operations Ensure segregation and removal of scrap material by coordinating with housekeeping Minimise scrap related hazards through the risk management processes Key Accountabilities (4/6) Maintain safety in the store operations by complying to safety norms to reduce the incidences and accidents Monitor the store assistants to use proper safety appliances while handling materials during receipt and dispensing Identify and report possible hazards and handle (storage, receipt , issuance) hazardous materials safely Key Accountabilities (5/6) Prepare receipts and issue materials on time by coordinating with purchase and user department to ensure required material is positioned in scheduled time Indent of materials as per correct quantity & delivery schedule from purchase department Manage material receipts while adhering to relevant SOP & store the goods as per the required storage condition Account the receipts of materials by making GRN Issue materials to user department by following SOP as per given schedule Key Accountabilities (6/6) Review stock of materials and store goods in appropriate conditions to reduce materials damage due to improper storage and for smooth production activity, and update in the system Monitor and record the environmental conditions of area and equipment Store the goods in designated places as per required storage conditions Carry out the reconciliation of reviewed physical stocks and update the effect of reconciled stocks in system Major Challenges Delay in delivery time due to frequent changes in the production plans and shifting priorities. Erratic delivery time by production. Overcome by conducting status meetings, escalation and continuous follow ups Delay in routine work due to system failure and issue of slips. Overcome by training from SMEs and manually working to reduce idle time Key Interactions (1/2) Manufacturing for dispensing planning (Weekly) Packing for prioritization of production (Weekly) Quality Control for release and sampling (Daily) Quality Assurance for discrepancies and non-conformances (Daily) Purchase for receipts (Daily) Accounts for invoice submission (Daily) Planning prioritize production (Daily) Customs for re-warehousing (Daily) Safety for safety norms and approval of destruction material (Daily) Engineering for maintenance issues (Daily) Housekeeping for sanitization (Daily) Key Interactions (2/2) Equipment Supplier for dispatch related (Need Basis) Transporters for deliveries (Need Basis) Courier for tracking of materials monthly Government authorities for stamping of weights (yearly) Pest Control Services for pest related issues (Daily) Dimensions (1/2) Average number of GRN for raw material / packing material : 300 per month Average number of materials removed (expired/rejection) : 50 per month Average number of dispatches : 30 per month Achieve internal OTIF more than 90% Achieve Zero reportable accidents / incidences during manufacturing Achieve 0% errors in online documentation Meet 100% compliance to SOP and safety regulations Maintaining proper storage condition (100%) 100% Clearance/disposal of non-moving/rejected materials Dimensions (2/2) Key Decisions (1/2) Bin Allocation Handling of material at designated place Set priority for dispensing of a particular material as per manufacturing requirements Set priority for unloading of vehicle of a particular consignment Key Decisions (2/2) Improvements in store operations, facility and documents to Section Head - Stores Education Qualification Graduate or D. Pharm Relevant Work Experience 0-2 years of experience with exposure to stores operations, preferably in a pharma company with regulatory approvals

To perform Machine and area clearance during dispensing, manufacturing and packaging operation. To perform sampling of blend, finished product, reserve sample, stability sample, hold time samples and other in-process samples and to manage sampling aids. To carry out in-process checks, AQL and ANSI Sampling as per respective documents viz. protocol,BMR, BPR, SOPs and other GxP documents. To ensure GMP practices at manufacturing shop floor. To verify raw material dispensing activity. To approve batch coding details during packaging operation. Review of executed batch records and release for next processing stage. Preparation and review of CPV data trend. To perform impact assessment of breakdown memo. To initiate change control, unplanned and planned deviation where ever required. To review area, equipment and cleaning log and to ensure proper labelling. To review environmental monitoring record, calibration records and executed Batch Manufacturing and packaging Records and respective electronic records. To perform calibration of IPQA instruments. To ensure appropriate labelling during manufacturing and packaging. Storage, handling and dispensing of printed packing materials. To review and approve packaging artworks, proofs and shade cards. To archive executed documents like BMR, BPR, Hold time Protocol etc. To review and approve the Quality Notification (Viz Change control and Deviation) during Batch Manufacturing/packaging. To monitor and record the environmental condition of label control room. To prepare and revise functional SOPs, wherever required. Activities other than defined in the Job Responsibility are to be done, as per the requirement of HOD, by following HODS instructions and guidance.

Creating Passion: Your Responsibilities Reponsibilites To carry out abrasive blasting operations for structural and precision components of tower cranes and drive systems to achieve the required surface cleanliness, roughness (anchor profile), and preparation standards prior to painting or coating processes. The Shot Blaster ensures proper surface preparation for long-term coating adhesion and corrosion resistance, as per technical and quality specifications (e.g., ISO 8501-1). Surface Preparation Perform shot/grit blasting on fabricated assemblies, machined components, or drive housing components. - Ensure uniform blasting to remove rust, scale, weld slag, oil, and previous coatings. Achieve the required surface cleanliness grade (e.g., Sa 2.5 / Sa 3) and anchor profile as specified in the technical specification sheet or paint system. Pre-Blasting Inspection Verify material identity using heat code / part ID prior to blasting. Ensure weld joints, oil marks, burrs, and surface damages are appropriately rectified before blasting. - Mask or protect critical surfaces (e.g., machined areas, threads, nameplates) from abrasive media using suitable masking tape or shields. Equipment Operation & Setup Operate manual/semi-auto blasting machines, including blasting pots, hoses, nozzle guns, recovery system, and dust collectors. - Adjust air pressure, nozzle size, and abrasive flow as per job card / SOP. Monitor compressor operation and airflow consistency during the job. - Ensure adequate lighting and ventilation inside blasting booths. Abrasive Media Handling Load, monitor, and maintain abrasive blasting media (e.g., steel shots, aluminum oxide). Ensure media cleanliness by screening and rejecting contaminated or broken grits. - Inform supervisor for replenishment of low media stock. Post-Blasting Inspection Conduct visual inspection of blasted surface for cleanliness, roughness, or missed areas. Reject and reblast areas that show flash rust, oil residue, under-blasting, or excessive pitting. Inform quality or paint department once surface is ready for primer application. Documentation & Traceability Record job number, component name, part number, heat number, blasting parameters, date, and operator initials on surface treatment records or Q-log sheet. Ensure traceability between raw material heat code and finished component at all stages. Tag components clearly post-blasting before transfer to paint. Maintenance & 5S Wear mandatory PPE: blasting helmet with air supply, earplugs, gloves, overalls, and steel-toe boots. Follow confined space entry protocols and ventilation system operation. Handle used abrasives and waste according to hazardous waste handling norms. Follow SOP in case of emergency (e.g., equipment burst, media exposure, fire). Coordination with Other Teams Coordinate with quality, paint, fabrication, and material handling teams for job sequencing. Report delay reasons, rejection causes, or equipment readiness status. Support continuous improvement or 8D problem-solving activities in case of quality issues. Contributing Your Strengths: Your Qualifications Qualification & Education Requirements: Minimum Education- ITI / NCTVT in Painter / Fitter / Fabrication / Surface Treatment or equivalent Preferred Vocational Training- Industrial Blasting, Abrasive Media Handling, Safety in Surface Treatment Additional Training / Certifications- SSPC/NACE Blaster Certification Level I (preferred) Internal training on ISO 8501-1, ISO 12944, ISO 11124 blasting standards (if available) Work Instruction Comprehension- Must be able to read and interpret job cards, pictorial SOPs, and technical paint/blasting parameters in English or local language Experience Industry Experience- Minimum 2 4 years in surface preparation/blasting operations in heavy fabrication, construction equipment, pressure vessels, or shipbuilding Equipment Experience- Hands-on with air pressure blasting pots, suction blasting, recovery & dust extraction systems Familiarity with Standards- ISO 8501 (surface preparation), ISO 11124 (abrasives), NACE/SSPC standards Safety Experience- Experience in working with full PPE, confined booth operation, ventilation, and safety interlocks Preferred Skills / Special Skills Equipment Usage- Authorized to operate blasting machine, compressor, and recovery systems after safety checks Job Execution- Authorized to proceed with blasting after verifying masking, fixture integrity, and job cards Process Escalation- Process Escalation Surface Readiness Confirmation- Can declare a part ready for paint based on visual inspection and blasting standards Maintenance Request- Authorized to raise maintenance ticket for preventive or breakdown repairs Safety Non-Compliance Reporting- Right to report any violation of EHS protocols or absence of PPE in area Job Priority Request- Can inform supervisor regarding job urgency or re-sequencing if dependent process is delayed Have we awoken your interest? Then we look forward to receiving your online application. If you have any questions, please contact Sonali Samal. One Passion. Many Opportunities. The company Liebherr CMCtec India Private Limited in Pune (India) was established in 2008 and started its manufacturing plant in its own facility on Pune Solapur Highway in 2012. The company is responsible for the production of tower cranes and drives. Location Liebherr CMCtec India Private Limited Pune India (IN) Contact Sonali Samal sonali.samal@liebherr.com shweta.shakrawarti@liebherr.com

Role & responsibilities To plan, manage and buy domestic and import specialty chemicals and materials, In line with sourcing strategy. To ensure materials are received on time, in full quantity and at most competitive rates and with acceptable quality standards. To identify new suppliers, Conduct supplier audits.

Job Description: Mechanical Inspector Raw Material & Forging Inspection Job Title: Mechanical Inspector Raw Material and Forging Inspection Location: Kolkata Job Summary: We are looking for a Mechanical Inspector with hands-on experience in raw material and forging inspection. This role involves incoming inspection of raw materials such as steel, aluminum, and alloys, as well as forged parts. The inspector will assess material certifications, dimensional accuracy, visual and surface defects, and ensure conformance to technical standards and specifications. Key Responsibilities: - Inspect incoming raw materials including bars, billets, plates, and forgings for dimensional and visual compliance. - Verify mill test certificates (MTC), heat numbers, chemical and mechanical properties against purchase specifications. - Perform hardness testing, grain flow inspection, and micro/macro structural evaluation (in coordination with lab). - Check forging defects like laps, folds, cracks, underfills, and surface decarburization. - Ensure traceability and proper marking of accepted materials and quarantining of rejected lots. - Coordinate third-party inspections, sample testing, and mechanical testing where applicable. - Utilize inspection instruments such as vernier calipers, micrometers, ultrasonic testers, and hardness testers. - Prepare inspection reports, NCRs, and maintain documentation for quality records. - Collaborate with procurement, engineering, and supplier quality teams to address non-conformances. - Follow safety and material handling procedures in the inspection area. Qualifications: - Diploma / Degree in Mechanical or Metallurgical Engineering. - 35 years of experience in raw material and forging inspection in a manufacturing or forging environment. - Understanding of metallurgy, forging processes, and inspection standards (e.g., ASTM, IS, EN). - Familiarity with NDT methods (UT, MPI, DPI) and grain flow orientation. - Ability to interpret material test certificates and engineering drawings. - Certified Level II in DP,VT & UT - Preferred Skills: - Knowledge of ISO 9001, IATF 16949, or AS9100 quality systems. - Hands-on experience with ERP or quality tracking software. - Basic understanding of material traceability and lot control.

1.Purchase of Raw material, consumable & general items 2.Securing favorable terms for pricing, delivery, and quality. 3.Ensuring optimal stock levels to meet demand & handle Stores. 4.Purchase of Raw material like SS, MS, CR & SS sheets. Required Candidate profile 5. Ensuring all purchases meet company policies and industry standards. 6. Budget Management: Managing procurement budgets effectively. 7. Candidate fromengineering industry preferred

Inventory Management: Monitor and manage food, beverage, and supplies inventory to reduce waste and ensure optimal stock levels. Conduct periodic stock audits and reconciliations. Cost Control & Analysis: Analyze food and beverage costs, identify trends, and recommend strategies to improve profitability. Develop cost-effective measures to minimize wastage without compromising quality. Standard Operating Procedures (SOPs): Implement and maintain SOPs for procurement, inventory control, and operational efficiency. Ensure compliance with company policies and industry regulations. Vendor Coordination: Collaborate with suppliers to ensure timely delivery of quality products at competitive prices. Evaluate vendor performance and negotiate contracts where necessary. Reporting & Analytics: Prepare detailed reports on inventory, sales, and cost analyses for senior management. Identify actionable insights and provide recommendations for improvement. Quality Assurance: Regularly inspect food and beverage quality to ensure consistency and adherence to brand standards. Support the Quality Assurance team in implementing best practices. Collaboration: Work closely with the operations, kitchen, and finance teams to align goals and improve overall efficiency. Support new outlet launches by setting up inventory and controls processes.

About Company Founded in 2011, ReNew, is one of the largest renewable energy companies globally, with a leadership position in India. Listed on Nasdaq under the ticker RNW, ReNew develops, builds, owns, and operates utility-scale wind energy projects, utility-scale solar energy projects, utility-scale firm power projects, and distributed solar energy projects. In addition to being a major independent power producer in India, ReNew is evolving to become an end-to-end decarbonization partner providing solutions in a just and inclusive manner in the areas of clean energy, green hydrogen, value-added energy offerings through digitalisation, storage, and carbon markets that increasingly are integral to addressing climate change. With a total capacity of more than 13.4 GW (including projects in pipeline), ReNew’s solar and wind energy projects are spread across 150+ sites, with a presence spanning 18 states in India, contributing to 1.9 % of India’s power capacity. Consequently, this has helped to avoid 0.5% of India’s total carbon emissions and 1.1% India’s total power sector emissions. In the over 10 years of its operation, ReNew has generated almost 1.3 lakh jobs, directly and indirectly. ReNew has achieved market leadership in the Indian renewable energy industry against the backdrop of the Government of India’s policies to promote growth of this sector. ReNew’s current group of stockholders contains several marquee investors including CPP Investments, Abu Dhabi Investment Authority, Goldman Sachs, GEF SACEF and JERA. Its mission is to play a pivotal role in meeting India’s growing energy needs in an efficient, sustainable, and socially responsible manner. ReNew stands committed to providing clean, safe, affordable, and sustainable energy for all and has been at the forefront of leading climate action in India. Job Description Review and approval of contractor’s FQAPs. Assuring implementation of Quality Plan. Inspection and audit of TL construction work including substation as per FQAP and checklists. Follow up of Quality observations/NCs and timely closure with contractor. Quality audits and Quality checks during erection of Towers. Quality inspection during stringing activity and experience in final checking of towers. Monitoring and planning the Site quality inspections through TPAs. Monitor and review all the Civil activities at site like material incoming, in-process activities, testing and commissioning. Inspection of Transmission line tower parts line templates angles and Bolts etc. Monitoring overall project quality control and quality assurance. Inspection of incoming materials (IMIR) Knowledge of relevant IS codes related to civil works. Preparation of NCs if any, find out root cause, proposed corrective action and suggest preventive action. Review of Drawings, SOP, FQP, Check list, etc. Implementing the QA/QC management system at the site. Provide daily & weekly feedback to project, and quality manager regarding progress reports, inspection & test status, quality issues & NC status. Preparing IMIR, Cube register, test reports for materials. Documentation and testing as per QAP & ITP Directly coordinating with the contractors regarding project activities such as construction, maintenance, support, documentation, and testing activities to ensure compliance with specifications, codes, and client requirements. Providing on job quality training. Reporting and documentation as per Indian Standards Auditing and documentation. Skills to do commissioning and testing. 3rd party inspector and contractor- management. Knowledge of Reinforced Cement Concrete, concrete cube test validation, NDT & core test. Knowledge of relevant IS codes of civil and structure works. Knowledge of raw material testing for civil construction works at site and lab.

Role & responsibilities Responsible for RM/PM Dispensing SAP Basic documentation Preferred candidate profile Pharmaceutical experience is a must. Interested candidates can share their CV/Resumes to noor.m.judge@zyduslife.com

Should be conversant in operations of Sliding Head, Multi spindle machines, CNC Lathes with minimum programming knowledge. Should have adequate knowledge of ISO -9000 systems For more details call - 8050070079

Job Description Responsible for receipt and storages of Raw and Packaging materials. Responsible for reconciliation Raw and Packaging materials. Responsible Cleaning and sanitization activities of classified area. all the activity of classified area including Area compliance etc. Responsible for various warehouse activity related activities like operation of Isolator, Operation of PAS-X system, operation of RLAF , Dispesning of Raw material & packaging materials and Calibration/Verification of weighing balances. Responsible for various audit compliances as required. Handling of Rejected materials. Handling Of FG Dispatch. Work Experience 1-6 Years. Education Graduation in Science or Science Diploma in Science or Science Competencies

Job Description Management of RM/PM/CM section including all required documents review and approval including timely support to manufacturing activity with cGMP compliance. Management of sample management section including all required documents review and approval including timely support to manufacturing activity with cGMP compliance. Preparation of SOP s/ STP s/ equipment URS/ Qualification/ Study protocols/ reports pertaining to RM/PM section. Review of equipment URS/ Qualification protocols/ reports pertaining to Raw Material/ Packaging Material/ Analytical section. The candidate should be conversant with Quality module of SAP system. Timely Updation of RM/PM/CM and water analysis results in SAP system. To ensure timely In-house calibration/ verification of RM/ PM/ Analytical equipment s as per the approved procedures and calibration/ verification frequency along with approved documentation. To ensure the testing of pre-purchased RM/PM/CM samples for Vendor qualification activity of newly identified vendors. The candidate should be conversant procedure for procurement of chemicals/ Reagents/ consumables and maintain their inventory records. To Ensure cGMP compliance in laboratory and ensure that the laboratory is always maintained in audit ready status. Work Experience 8 to 10 years Education Masters in Chemistry or Organic Chemistry Competencies