285 Jobs in Halol - Page 12

Analyze and optimize logistics costs to improve efficiency and reduce expenses.Manage diesel inventory and tracking as we have our own Diesel pump.Monitor incoming and outgoing diesel supplies.Maintain accurate records and data.

Product & tooling Design, Development,Prototyping & Testing of products meeting International regulations.Heading Design & development team.Responsible for business expansion by adding new products & new customers from Tractor & Trucks & Bus Segments Required Candidate profile Defining project description & budget in conjunction with Customer requirements.New Product Design & Development of Tractor & Bus driver Seats Suspension meeting International/Regulations for quality

Planning production activity on daily &weekly bases as per PPC.Ensuring various process r carried out as per standards.Rejection analysis.Layout change for improvement in production.Follow up material shortage & participation in Kaizen, Pokayoke.5S Required Candidate profile Ensure availability of relevant work instruction & process sheets.OEE Calculation.Manpower handling,SOP & employing TPM,WIP Control,PU chemical Knowledge.Maintenance Of PU Machine,PU process knowledge

Implementing lean mfg activity, Waste reduction,Cycle time reduction,Layout modification & preparing plant P&L.Leveraging skills implementing Plant manufacturing cost reduction plan to maintain cost contribution, monitoring overall resource capacity Required Candidate profile Leading production capacity planning as per 3M'S concepts.Monitoring process schedules & production orders w.r.t inventory,staffing requirements,work procedures & duty assignments in IATF Environment

Procurement BOPs as per PPC Plan & Inventory Norms,releasing schedules 2 Vendors & Performance Evaluation monthly basis & send VPR 2 suppliers.Local & Outstation Inventory Control as per inventory norms & focus on increasing Inventory Turn Ratio,MIS Required Candidate profile Kaizen & 5S Activity. Must be aware of working in Perpetual inventory environment, also high Inventory turnover ratio. Managing high turnover inventory.

Sun Pharmaceutical Industries Limited WALKIN DRIVE @ BARODA Function : MS&T - Injectable Experience : 1 to 6 years Qualification : B.Pharm/M.Pharm Job Location : Halol - Gujarat Date of Interview : 11th May 2025 || Time : 9.30 am - 1.00 pm. Venue of Interview : Sun Pharmaceutical Industries Limited, Near Akshar Chowk, Tandalja Road, Vadodara - 390012 Job Description: Execution of technology transfer to Sun/CMO Site transfer, Scale up, Exhibit, Process validation batches plan with effective planning and utilization of men, materials and machineries. Documentation work like new production introduction form, Scale-up reports, review of Sun/CMO BMR, sampling plan, PV protocol, URS preparation, and Dashboard preparation. To ensure that product is produced and stored according to the appropriate documentation in order to btain the desired quality. Responsible for Review & comments of MF, FMEA, RA & protocol (Sampling plan, Process validation protocol) and compliance. Handling & Support of Trouble shooting batches for data comparison and route cause Investigation at Sun/CMO. Investigation for product trouble shooting To ensure that the Packing operations or activities are carried out on timely. To monitor & prior checkup of equipment planned for usage in Scale up, Exhibit, Process validation batches i.e. Equipment preparation, vial washing & dehydrogenation, CIP/SIP System, PLCs, instruments etc. Responsible for Supervise and perform skid trials for better product development and process improvements and also minimizing manufacturing related constraints in future. To prepare the Scale up report, get evaluated and signed by authorized person prior going to Exhibit batches & their submitted to QA. Responsible to help the officers and operators to standardize production activities to achieve better efficiency and quality. To review validation protocol, SOP and other cGMP Documents. Close coordination with all the supporting departments i.e. Production, NPQC, QA, QE (Engineering) and warehouse for smooth running of Scale up, Exhibit, Process validation batches. To ensure the compliance of various in-process control instructions provided in MF, FMEA, RA, BMR, and MBMR.

Role & responsibilities Degree/Diploma in Engineering or Industrial Safety. Certified in ADIS or equivalent safety qualifications. 47 years of relevant safety experience in a foundry or heavy manufacturing environment. Sound knowledge of foundry hazards (e.g., heat, molten metal, dust, noise). Familiarity with Gujarat state regulations and the Factory Act. Strong communication, leadership, and problem-solving abilities. Proficiency in MS Office and EHS reporting tools. Preferred candidate profile Ensure adherence to all statutory and company-specific safety regulations and protocols. Conduct routine inspections of foundry processes (melting, pouring, core making, fettling, etc.) to identify and mitigate risks. Develop, implement, and monitor EHS policies, risk assessments, and safety improvement plans. Investigate incidents and near-misses, prepare detailed reports, and implement corrective actions. Organize regular safety training and toolbox talks for all employees and contractors. Maintain safety records, including inspection checklists, training logs, and incident reports. Ensure compliance with ISO 45001, Factory Act, and GPCB/PCB safety guidelines. Coordinate emergency response drills (fire, spill, evacuation) and ensure readiness of all safety equipment. Monitor and enforce proper use of PPE, safety signage, and lockout/tagout procedures. Liaise with government authorities during inspections, audits, and accident investigations.

Role & responsibilities Shop floor experience is required in the Tablets and Capsules section and sound knowledge of solid oral equipment functioning and operating principle Perform real-time monitoring of manufacturing and packaging processes to ensure adherence to GMP, SOPs, and regulatory requirements. Conduct in-process checks for critical quality attributes (e.g., weight, hardness, uniformity, and packaging integrity) at defined stages of production. Ensure timely documentation and approval of batch manufacturing records (BMR) and batch packaging records (BPR). Lead and coordinate qualification activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for equipment and utilities. Develop and review qualification protocols and reports, ensuring compliance with engineering and quality standards. Support the validation of facilities, equipment, and systems, including HVAC, water systems, and compressed air systems. Collaborate with the engineering team to ensure equipment and systems meet quality and regulatory requirements. Perform risk assessments for engineering processes, focusing on critical quality aspects during design and operational phases. Support maintenance and calibration activities by verifying adherence to predefined quality standards and documentation requirements.

Role & responsibilities Hands on experience required on handling of Process validation and Cleaning validation Design and execute validation protocols for process and cleaning validation activities, including IQ (Installation Qualification), OQ (Operational Qualification), PQ (Performance Qualification), and CV (Cleaning Validation). Develop and maintain a validation master plan (VMP) that aligns with regulatory requirements and organizational goals. Conduct process validation studies to ensure manufacturing processes consistently produce products that meet predefined quality attributes. Analyze process performance and critical parameters during validation runs and document results. Ensure adherence to Good Manufacturing Practices (GMP) during all validation activities. Develop and execute cleaning validation protocols to confirm the effectiveness of cleaning procedures in removing residues, contaminants, and microorganisms. Establish acceptable residue limits and cleaning verification procedures based on product toxicology and batch size. Monitor cleaning practices and perform periodic revalidation as required.

Role & responsibilities Experience required in Quality Control Laboratory and investigation of OOS/OOT/LIR/OOC, with expertise in reviewing analytical documents such as AMV protocols and reports. Experience with analytical techniques like HPLC, GC, FTIR, and UV-Vis spectroscopy. Prior exposure to quality management systems and laboratory automation tools. Perform detailed investigations for OOS, OOT, LIR, and OOC results. Identify root causes and propose effective corrective and preventive actions (CAPA). Document investigation outcomes clearly and ensure timely resolution.