199 Jobs in Jadcherla - Page 4

R Key Responsibilities and Skills: Assisting in Electrical Work : Junior electricians work alongside experienced electricians, helping with tasks like wiring, installing fixtures, and repairing equipment. Troubleshooting : They learn to diagnose electrical problems and assist in finding solutions. Safety Compliance : Adhering to safety regulations and using tools safely is a critical aspect of the job. Reading Blueprints : Understanding technical drawings and schematics is essential for planning and executing electrical work. Documentation : Keeping records of work completed and materials used is part of the job. Communication : Junior electricians need to be able to communicate effectively ...

Key Responsibilities: Installation and Maintenance : Installing, maintaining, and repairing utility systems, including water lines, gas pipes, electrical wiring, and waste management infrastructure. Troubleshooting and Repair : Diagnosing and fixing problems with utility systems, minimizing downtime and service interruptions. Inspections and Preventative Maintenance : Conducting regular inspections and performing preventative maintenance to ensure systems operate efficiently and reliably. Record Keeping and Documentation: Maintaining accurate records of maintenance activities, system updates, and compliance with safety regulations. Emergency Response : Responding to emergency calls and addre...

Role & responsibilities Production - Autoclave, Compounding, filling, QMS, Vial Washing, Lyophilizer QC-Micro - EM, Water Testing, Product Analysis (MLT & Sterility) Engineering - Process Maintenance (Mech & Instrumentation) with scope of Sterile Equipments & Calibration

Company Description LEESA LIFESCIENCES PRIVATE LIMITED is a mining and metals company located in Jadcherla, Mahbubnagar, Telangana, India. Our company operates out of several sites and specializes in innovative solutions in the mining and metals sector. We are committed to sustainable practices and excellence in the field, aiming to set new standards in the industry. Role Description This is a full-time on-site role for a Civil Engineer located in Jadcherla. The Civil Engineer will be responsible for performing civil engineering design, planning, and stormwater management. Day-to-day tasks include drafting, reviewing project drawings, managing construction projects, and ensuring compliance w...

Boiler Operation:Operate and control high-pressure boilers to generate steam or hot water Monitor boiler gauges, meters, and controls to ensure proper functioning Safety Compliance:Adhere to safety protocols and guidelines for boiler operation Conduct regular safety checks and inspections to prevent accidents Equipment Monitoring:Monitor and adjust boiler parameters to maintain optimal efficiency and performance Respond to alarms or abnormalities in the operation of the boiler Maintenance:Perform routine maintenance tasks, such as cleaning, lubricating, and replacing worn components Schedule and oversee periodic inspections and repairs Water Treatment:Manage water treatment processes to ensu...

HIRING FOR OSD - PRODUCTION & QC PRODUCTION(OSD) Experience: (01-07Years) Compression, Granulation, Coating, Capsule filling, Inspection QC Experience: (02-09Years) HPLC, GC, RM,PM, Stability, IP/FP, Method Development, Method Transfer QUALIFICATION : ITI/DIPLOMA/BSC/MSC/B PHARM/M PHARM With relevant Experience ITI/DIPLOMA/BSC/MSC/B PHARM Freshers can Apply DESIGNATIONS: Operator/Sr Operator/Jr Officer/Officer/Jr Executive/Executive INTERVIEW VENUE: SK Consultancy Services, H.No-1-77, 3rd Floor, Bachupally X Road, Opposite Sri Swastik Multi Specialty Hospital, Towards Nizampet Road DATE &TIME: 26th July 2025 ( Saturday); From 09.00 A.M. to 03.00 P.M NEED TO CARRY: Resume 3 Month Pay slips In...

We are seeking a visionary Plant Head to revolutionize operational excellence. As a pivotal leader, you will drive the company's mission to deliver high-quality pharmaceutical solutions worldwide. Collaborating with cross-functional teams, including tech transfer, sales, and quality control, you will ensure seamless operations and timely dispatches. This role offers a unique opportunity for professional growth, with exposure to global markets and cutting-edge pharmaceutical practices. Must-Have Master's degree (Preferred), 25+ years of experience, Expertise in Production Planning, Quality Control, and Engineering Management, Experience in Regulatory Compliance Exposure to Contract Manufactur...

Role & responsibilities : Only for male candidates Shri Kartikeya Pharma [Jadcherla / India] located in JADCHERLA TELANGANA, India had its last known inspection on 04 Jan 2024. There are 1 known inspections on record Preferred candidate profile Freshers,1-2 yrs

Role & responsibilities Plant overheads accounting. Imprest & advances analysis & recovery. Statutory compliances as per calendar GST & TDS and Returns GST Working Departmental MIS . Handling receivables and payables Maintaining minimum cash balance & making it available to meet day-to-day plant requirements. Release of salaries at the latest by 7th of next month Preferred candidate profile : Strong Knowledge in Finance & Accounting , statutory compliance , GST & TDS returns.

Job Title Executive/Sr Executive Environment, Health & Safety (EHS) and ETP Role Overview An executive-level role responsible for steering the companys EHS strategyensuring workplace safety, environmental compliance, and the effective operation of the Effluent Treatment Plant (ETP). This position oversees all EHS and ETP activities, integrates them into the broader pharmaceutical manufacturing process. Key Responsibilities 1. EHS Leadership & Strategy Develop EHS policies aligned with ISO 14001/45001 standards and corporate sustainability goals Lead EHS team in risk assessments, audits, incident investigations, and corrective actions Drive safety culture via training, toolbox talks, Gemba wa...

Job Title HotMelt Extruder Operator OSD Pharmaceutical Production Company Overview We are a leading pharmaceutical manufacturer specializing in continuous oral solid dosage (OSD) products. Our facility utilizes hot-melt extrusion Key Components of the Extruder in Granulation Feeder : Delivers the powders or wet granulation material to the extruder barrel. Screw : The screw inside the barrel performs the compaction, mixing, and shearing functions. The screw is typically a caterpillar screw or conveyor screw . Barrel : The barrel houses the screw and is where the material undergoes compaction and mixing. Die Plate : The plate with holes that shapes the extruded material into strands or granule...

Responsible for following activities in purification area of BM/BU based on campaign basis 1. Following GMP, safety practices in production facilities and work place. 2. Responsible for production activities: Execution of area, line clearance before execution of activities. Execution of product changeover activities. Responsible for column cleaning, packing, unpacking, evaluation and maintenance. Responsible for drug substance (FDS) transfer/dispensing. Execution of production activities. Monitoring and review of batch parameters/performance. Ensuring material are arranged properly before activities. Verification of samples for analysis. Responsible for shift Monitoring. Handling of online r...

1. Responsible for operation and cleaning of Vial washing machine, Depyrogenating tunnel, Vial / PFS filling stoppering machine, vial sealing collection machine and Lyophilizer. 2. Responsible for involvement in aseptic media fills formulation and filling activities in aseptic areas. 3. Responsible for operation and cleaning of HPHV Steam sterilizer. 4. Responsible for cleaning, preparation of components as per load pattern. 5. Preparation and filtration of disinfectants, IPA etc., 6. Responsible for area and equipments cleaning in FP facility. 7. Handling of APA equipments and to be involved in personnel gowning qualification. 8. Online Execution of Batch documents and related logbooks. 9. ...

1. Responsible for review of specifications, STPs, GTPs and analytical test data sheets. 2. Review of analytical reports of raw material, packing materials, water samples, product samples, OOT, water trends and ensuring compliance. 3. Responsible to attend the training programs. 4. Responsible for monitoring of quality control Lab (Daily calibration, PMP, Instruments back up data, Excel work sheets lock, user log books). 6. Responsible for handling technology transfer documents. 7. Responsible for review of stability protocols, stability analytical data and summary reports. 8. Responsible for handling of change controls, OOS, OOT, Incidents and investigations. 9. Responsible for compliance o...

1. Responsible for preparation of Validation Master Plan, validation related SOPs and schedules. 2. Responsible for preparation of facility, equipment, area qualification protocols and reports. 3. Responsible for execution of facility, equipment and area qualification activities. 4. Responsible for compilation and review of validation raw data and test certificates. 5. Responsible for preparation and review of Computerized system validation (CSV) documents and execution of CSV for equipments. 6. Responsible for preparation of User Requirement Specification, Design Qualification, FAT protocols, SAT protocols, Installation qualification, Operational qualification and Performance qualification,...

1. Responsible for operation and cleaning of HPHV steam sterilizer 2. Responsible for operation and cleaning of vial washing machine and depyrogenation tunnel. 3. Responsible for cleaning, preparation of filling machine parts and load patterns. 4. Responsible for washing, drying and preparation of garments for manufacturing areas. 5. Preparation and filtration of disinfectants, IPA etc. 6. Cleaning of equipments and rooms in processing areas. 7. Online Execution of Batch documents and related logbooks. 8. Handling of various type of filters and filter integrities. 9. Participate in qualification of equipments (DQ, IQ, OQ and PQ) in manufacturing areas. 10. Execution of production related act...

1. Preparation, review and revision of SOPs, GTPs and Work sheets. 2. Execution of analytical method validation protocols for product samples. 3. Testing and review of product / Miscellaneous samples for AET. 4. Operation and maintenance of laboratory Instruments. 5. Monitoring of temperature, DP and RH of the Microbiology laboratory. 6. Involve in the execution of Media fill validations. 7. Cleaning, verification of laboratory cleaning and glassware cleaning in the Microbiology laboratory. 8. Receipt, storage, preparation, sterilization and maintenance of sterile media and reagents. 9. Performing the isolation, identification and confirmation tests for test organisms and Isolates. 10. Respo...

Planning and executing assay-runs for cell based assays and ELISA as part of Method Development and Method Qualification studies Analysis of the data using parallel line analysis and equivalence testing Writing protocols and reports for Method development and Method qualification studies Maintenance of the cell lines, preparation of cell banks Review of raw data and data recording sheets and to ensure good documentation practices. Planning of day-to-day activities independently. Trouble shooting of the issues (if any) aroused during execution of assay-run. Involving in documents preparation for SOP, STP, MOA.

1. Preparation and Maintenance of SOPs, STPs, Specifications, GTPs and Worksheets related to Product testing. 2. Preparation, revision, review and execution of Analytical method Validation protocols and reports related to product testing. 3. Responsibilities for preparation of masters (Product, Specifications, Tests, worksheets, Test plans and TTD etc.) in LIMS. 4. Responsibilities for effective documents (STPs, Specifications and GTPs etc.) uploaded in LDMS. 5. Responsible for material management like weekly, monthly indent Ensure monthly indents are placed and materials received in timely manner, reservation placed through SAP. Ensure compliance `w.r.t expiry, usage and discard of material...

1.Responsible for giving line clearance between startup of various finished product formulation and filling operations. 2.Responsible for performing in process checks during finished product operations as per respective established procedures. 3.Responsible for Monitoring and Coordination of process validation, Hold time studies, media fill and cleaning validation activities. 4. Responsible for preparation of IPQA SOPs and review of finished product SOPs. 5. Responsible for preparation of Annual Product Review Reports. 6. Responsible for continued process verification reports. 7.Responsible for compliance to GMP in finished product area. 8.Responsible for review of all finished product log b...

1) Development of mass spectrometry based methods for analysis of various molecules for pivotal studies such as biosimilarity, comparability etc.. 2)operation and maintenance of mass spectrometry instrument and performing troubleshooting activities 3)developing and carrying out multiple assays aimed at characterization of protein based therapeutics across various stage of the project 4) participate in design, development and implementation of methods for CQA/impurity characterization of molecules. Interpret results,and draw conclusions from multiple stage experiments 5) Author technical documents such as SOP,MoA,study protocol and reports for method and product development

1. Responsible for operation and cleaning of HPHV steam sterilizer 2. Responsible for operation and cleaning of vial washing machine and depyrogenation tunnel. 3. Responsible for cleaning, preparation of machine parts and load patterns. 4. Responsible for Washing and preparation of garments for manufacturing areas. 5. Preparation and filtration of disinfectants, IPA etc. 6. Cleaning of equipments and rooms in processing areas. 7. Online Execution of Batch documents and related logbooks. 8. Handling of various type of filters and filter integrities. 9. Participate in qualification of equipments (DQ, IQ, OQ and PQ) in manufacturing areas. 10. Execution of production related activities and achi...

1. Aseptic handling. 2. Media and feeds preparation for shake flasks experiment and bioreactors batches. 3. Shake flasks handling for clone, media and feed selection. 4. Bioreactors preparation (1L,5L,20L). 5. Batch execution in small scale bioreactors and large-scale bioreactors. 6. In process sample analysis like cell count, viability, metabolites (glucose, lactate, ammonia, glutamine etc. 7. SOP preparation related to instruments and process. 8. Shift duties for batch monitoring. 9. Able to work in a team.

The candidate would be developing various analytical method (such as CD, Fluorescence spectrscopy ,CE UH/HPLC etc..)for CQA to support biosimilarity and analytical studies. Qualify method for biosimilarity and analytical studies. Responsible for performing biosimilarity, characterization and analytical studies for various molecules across lifecycle . Evaluation, interpretation and graphical representation of the measurement data as well as presentation of the results obtained from multiple experiments. Author technical documents such as MoA,MQR,SOP,study protocol and report.

1. To perform Area cleaning. 2. To perform Equipment operation and cleaning. 3. To perform the visual inspection and packing activities. 4. To perform the documentation as per Batch record and SOP. 5. Responsible to maintain documents as per cGMP norms. 6. Ensure the training completion before doing activity. 7. Maintain personal hygiene. 8. Reporting all the activities, incidents and problems to Reporting officer.