109 Autoclave Jobs - Page 3

Role & responsibilities: Set up and operate lyophilization machines, autoclave and all related equipments Record all relevant data on batch logs to ensure traceability and for compliance with regulations. Identify and address any equipment malfunctions, such as temperature deviations or pressure irregularities, which could affect product quality. Perform routine maintenance tasks like cleaning, calibrating, and troubleshooting the lyophilizers, ensuring the equipment remains in optimal working condition. Work with the maintenance team to resolve any more complex equipment issues.

Role & responsibilities To be part of a leading pharma company To be part of Injectable production department. Preferred candidate profile Diploma or 10+2 with more 1 year of relevant experience Perks and benefits Best in industry Transport Facility Medical Insurance

Walk-In Interview Date : 06 th April 2025 (Sunday) Timing : 9.00 AM to 1.30 PM Venue : Umedica Laboratories Pvt, Ltd. Plot No 221, II Phase GIDC Nr Morarji Circle, Vapi 396195. 1. Tablet Manufacturing Department: Ability to handle process like Dispensing, Granulation, Compression, Coating, SOPs preparation, well versed with ALCOA & GDP principles. QMS Manufacturing investigation (OOS/OOT/Deviation/CAPA),Training.) Position: Officer to Sr. Officer Qualification: M.Sc. / B.Pharma / M.Pharma No. of Vacant Position: 20 Experience: 2 to 4 years To Operate Granulation lines (RMG/FBD/FBP/Roll Compactor), Automatic Compression Machine (PLC/SCADA based Cadmach & Fluid Pack), Coating (Kevin & Gansons) Position :Technical Associates (Operator) Qualification: ITI / Diploma Experience: 1 to 4 years No. of Vacant Position: 15 2. Tablet Packing Department: Should have sound knowledge in SOPs, BPR, Line Clearance, Daily formats &records, Manpower Handling GDP, GMP. Position: Officer to Executive Qualification: B.Pharma / M.Pharma No. of Vacant Position: 10 Experience: 2 to 9 years(To Operate Blister Pack Machine ELMACH 3015 PDA machine/ IC 150C / WKH100 Cartonator machine/ Track and Trace machine with Temper Evident., CVC Primary & Secondary) Position: Technical Associates (Operator) Qualification: ITI / Diploma Experience: 2 to 5 years No. of Vacant Position: 15 3. Injectable Department: (Should have sound knowledge require in SVP, Aseptic Vial & Ampule filling, Washing, Autoclave & Sterilization. ) Position: Officer to Executive Qualification: B.Pharma / M.Pharma/ M.Sc. No. of Vacant Position: 05 Experience: 3 to 6 years Should Have Knowledge of ampule filling , Liquid vial Filling Machine , Rotary Vial Washing Machine , Bung Processor Steam Sterilization Position: Operator & Technical Associate Qualification: I.T.I / D.Pharma Experience: 1 to 7 years No. of Vacant Position: 05 4 . Quality Control Department: Candidates having educational qualification of BSc/MSc with specialization in Chemistry. Organic chemistry/Analytical chemcistry with experience of 2 to 7 years in Quality control departments. Working exposure in HPLC, GC, UV Vis spectrophotometer, FTIR, Melting point, Dissolution Apparatus etc with regulatory exposure of USFDA/MHRA/EU/Brazil ANVISA/TGA/WHO audit. .) Position: Officer to Sr. Officer Qualification: M.Sc. / B.Sc. Experience: 1 to 5 years No. of Vacant Position: 15 6. QA Department: (Should have sound knowledge in IPQA (Tablet Manufacturing / Packing/Injection)Training & QMS Activities Position: Officer to Sr. Officer Qualification: B.Sc / M.Sc. / B.Pharm / M.Pharm Experience: 1 to 6 years No. of Vacant Position: 05 7. TTD Department: Preparation of plan regarding transfer of process / product from development, scale-up, manufacturing of exhibit / submission, launch to post approval phase which shall encompass the quality aspects (including risk assessment principles) and necessary regulatory requirement aspects. Co-ordination between R & D / client (product transferring unit) and all applicable stake holder departments in the plant (receiving unit) so as to ensure the smooth and effective transfer of product. Position: Officer to Sr. Officer Qualification: / B.Pharm / M.Pharm Experience: 1 to 6 years. No. of Vacant Position: 03 8. Warehouse Department: Should have sound knowledge of SAP Activities , Handling of QMS related activities, Handling of Purchase Order , Purchase Requisition, GRN, RM, PM. Position: Officer to Sr. Officer Qualification: / B.Com / M.Com /BCA Experience: 1 to 6 years. No. of Vacant Position: 03 Kindly carry below listed documents during interview. 1. Latest Passport size photo 2. Latest updated resume 3. Xerox copy of Qualification Certificates 4. Salary Slip / Appointment letter copy of current company / CTC Proof

? Do Support process by managing transactions as per required quality standards Fielding all incoming help requests from clients via telephone and/or emails in a courteous manner Document all pertinent end user identification information, including name, department, contact information and nature of problem or issue Update own availability in the RAVE system to ensure productivity of the process Record, track, and document all queries received, problem-solving steps taken and total successful and unsuccessful resolutions Follow standard processes and procedures to resolve all client queries Resolve client queries as per the SLA’s defined in the contract Access and maintain internal knowledge bases, resources and frequently asked questions to aid in and provide effective problem resolution to clients Identify and learn appropriate product details to facilitate better client interaction and troubleshooting Document and analyze call logs to spot most occurring trends to prevent future problems Maintain and update self-help documents for customers to speed up resolution time Identify red flags and escalate serious client issues to Team leader in cases of untimely resolution Ensure all product information and disclosures are given to clients before and after the call/email requests Avoids legal challenges by complying with service agreements

? Do Support process by managing transactions as per required quality standards Fielding all incoming help requests from clients via telephone and/or emails in a courteous manner Document all pertinent end user identification information, including name, department, contact information and nature of problem or issue Update own availability in the RAVE system to ensure productivity of the process Record, track, and document all queries received, problem-solving steps taken and total successful and unsuccessful resolutions Follow standard processes and procedures to resolve all client queries Resolve client queries as per the SLA’s defined in the contract Access and maintain internal knowledge bases, resources and frequently asked questions to aid in and provide effective problem resolution to clients Identify and learn appropriate product details to facilitate better client interaction and troubleshooting Document and analyze call logs to spot most occurring trends to prevent future problems Maintain and update self-help documents for customers to speed up resolution time Identify red flags and escalate serious client issues to Team leader in cases of untimely resolution Ensure all product information and disclosures are given to clients before and after the call/email requests Avoids legal challenges by complying with service agreements

? Do Support process by managing transactions as per required quality standards Fielding all incoming help requests from clients via telephone and/or emails in a courteous manner Document all pertinent end user identification information, including name, department, contact information and nature of problem or issue Update own availability in the RAVE system to ensure productivity of the process Record, track, and document all queries received, problem-solving steps taken and total successful and unsuccessful resolutions Follow standard processes and procedures to resolve all client queries Resolve client queries as per the SLA’s defined in the contract Access and maintain internal knowledge bases, resources and frequently asked questions to aid in and provide effective problem resolution to clients Identify and learn appropriate product details to facilitate better client interaction and troubleshooting Document and analyze call logs to spot most occurring trends to prevent future problems Maintain and update self-help documents for customers to speed up resolution time Identify red flags and escalate serious client issues to Team leader in cases of untimely resolution Ensure all product information and disclosures are given to clients before and after the call/email requests Avoids legal challenges by complying with service agreements

? Do Support process by managing transactions as per required quality standards Fielding all incoming help requests from clients via telephone and/or emails in a courteous manner Document all pertinent end user identification information, including name, department, contact information and nature of problem or issue Update own availability in the RAVE system to ensure productivity of the process Record, track, and document all queries received, problem-solving steps taken and total successful and unsuccessful resolutions Follow standard processes and procedures to resolve all client queries Resolve client queries as per the SLA’s defined in the contract Access and maintain internal knowledge bases, resources and frequently asked questions to aid in and provide effective problem resolution to clients Identify and learn appropriate product details to facilitate better client interaction and troubleshooting Document and analyze call logs to spot most occurring trends to prevent future problems Maintain and update self-help documents for customers to speed up resolution time Identify red flags and escalate serious client issues to Team leader in cases of untimely resolution Ensure all product information and disclosures are given to clients before and after the call/email requests Avoids legal challenges by complying with service agreements

? Do Support process by managing transactions as per required quality standards Fielding all incoming help requests from clients via telephone and/or emails in a courteous manner Document all pertinent end user identification information, including name, department, contact information and nature of problem or issue Update own availability in the RAVE system to ensure productivity of the process Record, track, and document all queries received, problem-solving steps taken and total successful and unsuccessful resolutions Follow standard processes and procedures to resolve all client queries Resolve client queries as per the SLA’s defined in the contract Access and maintain internal knowledge bases, resources and frequently asked questions to aid in and provide effective problem resolution to clients Identify and learn appropriate product details to facilitate better client interaction and troubleshooting Document and analyze call logs to spot most occurring trends to prevent future problems Maintain and update self-help documents for customers to speed up resolution time Identify red flags and escalate serious client issues to Team leader in cases of untimely resolution Ensure all product information and disclosures are given to clients before and after the call/email requests Avoids legal challenges by complying with service agreements

? Do Support process by managing transactions as per required quality standards Fielding all incoming help requests from clients via telephone and/or emails in a courteous manner Document all pertinent end user identification information, including name, department, contact information and nature of problem or issue Update own availability in the RAVE system to ensure productivity of the process Record, track, and document all queries received, problem-solving steps taken and total successful and unsuccessful resolutions Follow standard processes and procedures to resolve all client queries Resolve client queries as per the SLA’s defined in the contract Access and maintain internal knowledge bases, resources and frequently asked questions to aid in and provide effective problem resolution to clients Identify and learn appropriate product details to facilitate better client interaction and troubleshooting Document and analyze call logs to spot most occurring trends to prevent future problems Maintain and update self-help documents for customers to speed up resolution time Identify red flags and escalate serious client issues to Team leader in cases of untimely resolution Ensure all product information and disclosures are given to clients before and after the call/email requests Avoids legal challenges by complying with service agreements

? Do Support process by managing transactions as per required quality standards Fielding all incoming help requests from clients via telephone and/or emails in a courteous manner Document all pertinent end user identification information, including name, department, contact information and nature of problem or issue Update own availability in the RAVE system to ensure productivity of the process Record, track, and document all queries received, problem-solving steps taken and total successful and unsuccessful resolutions Follow standard processes and procedures to resolve all client queries Resolve client queries as per the SLA’s defined in the contract Access and maintain internal knowledge bases, resources and frequently asked questions to aid in and provide effective problem resolution to clients Identify and learn appropriate product details to facilitate better client interaction and troubleshooting Document and analyze call logs to spot most occurring trends to prevent future problems Maintain and update self-help documents for customers to speed up resolution time Identify red flags and escalate serious client issues to Team leader in cases of untimely resolution Ensure all product information and disclosures are given to clients before and after the call/email requests Avoids legal challenges by complying with service agreements

Responsible for the availability of raw materials, catalysts and instrument spares as per high pressure lab requirements. To analyse quality results and discuss the experimentation plan and parameters with Research Incharge. Understand the safety aspects of all reactions, chemicals and catalysts to be used in high pressure reactions. Ensure the proper setup ( compatability of autoclave, high pressure addition pumps, thermostats etc) as planned. Carry out reaction process as per the provided plan, get the analysis done for raw materials, catalysts , in process reaction intermediates and product. Record all observations and give suggestions for improvement. Report any breakdown, abnormal functioning of instruments in high pressure lab. Ensure proper housekeeping of the lab. Maintain highest safety practices while working by using required PPEs (Personal protective equipment). Maintain the log sheets of all the experiments regularly with critical observations and feed the data into Electronic Lab Notebook (ELN). Ensure working in lab as per SOP's provided. Maintain stock of all the chemicals, catalysts and instrument spares required as per 5'S' (sort, set-in-order, shine, standardize, sustain) After reaction completion, decontaminate the autoclave/instruments properly. To ensure proper and complete recovery/quenching of catalysts after reaction. To ensure proper and safe storage of catalysts and maintain its record. Segregate effluents as per the lab system. To undergo trainings as per schedule. Roles and Responsibilities Note:- Experience in High pressure Lab is must

Job Description Position : HVAC Technician/Engineer/ Officer Pharma Vaccine Manufacturing Company : GreenSignal Bio Pharma Pvt Ltd Location : Gummidipoondi, Chennai, Tamil Nadu Employment Type: Full-Time Experience : Minimum 3+ years as an HVAC Engineer/ officer/ Technician (preferably in the pharmaceutical industry) Educational Qualification: Diploma / Bachelor's / Master’s degree in Mechanical, Electrical, HVAC, or a related field Job Summary: The HVAC Technician / Engineer/ Officer will be responsible for the installation, maintenance, and troubleshooting of HVAC systems within the pharmaceutical cleanroom environment . The role requires expertise in GMP compliance, temperature control, differential pressure monitoring, and air quality management to support vaccine manufacturing operations. Roles & Responsibilities: 1. HVAC System Installation & Preventive Maintenance Install, inspect, and maintain Air Handling Units (AHUs), chillers, cooling towers, ventilation systems, and HVAC ducting . Perform routine preventive maintenance to optimize HVAC system performance. Diagnose and troubleshoot mechanical, electrical, and airflow issues in HVAC systems. 2. Cleanroom HVAC & Contamination Control Ensure temperature, humidity, and pressure differentials meet pharmaceutical cleanroom standards. Maintain HEPA filtration systems and oversee regular filter replacements. Ensure compliance with ISO 14644 cleanroom classifications and GMP guidelines. 3. Air Distribution & Ventilation Management Maintain air distribution systems, including ducting, dampers, diffusers, and exhaust systems . Monitor and maintain fume hoods, dust extraction systems, and air showers . Ensure proper functioning of differential pressure monitoring systems for contamination control. 4. Refrigeration & Cooling Systems Maintenance Conduct regular servicing of water-cooled and air-cooled chillers . Oversee the operation and maintenance of cooling towers, condensers, and refrigeration units . Ensure compliance with energy efficiency standards and refrigerant handling protocols . 5. Compliance, Validation & Documentation Perform calibration and validation of HVAC equipment to meet GMP and regulatory requirements . Maintain detailed records of service logs, maintenance reports, and HVAC validation documents . Support internal and external audits by providing necessary HVAC system documentation. 6. Building Management System (BMS) & Automation Operate and monitor BMS-controlled HVAC systems for real-time performance tracking. Assist in troubleshooting automation systems and HVAC control units . Ensure accurate logging of HVAC parameters in the Building Management System. Key Skills & Competencies: Strong knowledge of GMP, ISO 14644, and ASHRAE standards for pharmaceutical HVAC systems. Expertise in HVAC troubleshooting, preventive maintenance, and calibration . Hands-on experience with cleanroom HVAC systems and contamination control . Ability to work effectively in a fast-paced, regulated environment . Strong problem-solving and analytical skills . Excellent teamwork and communication skills . Willingness to stay updated with industry advancements in HVAC technology. Why Join Us? Opportunity to work in a leading pharmaceutical company. Career growth in the specialized field of pharmaceutical HVAC operations. Competitive salary and benefits. Be part of a team contributing to vaccine manufacturing and healthcare innovation. About GreenSignal Bio Pharma Pvt Ltd: GreenSignal Bio Pharma Pvt Ltd is a leading pharmaceutical company specializing in vaccine manufacturing . Our commitment to innovation, compliance, and operational excellence drives our success in delivering high-quality healthcare solutions. For more information, visit: www.gsbpl.com Interested candidates can apply at: hr@gsbpl.com Contact us at: 8778926365 Apply now and be a part of our team driving pharmaceutical innovations

Roles and Responsibilities - Vial Operator 1. Operate the Vail/ Cartridge filling Machine. 2. Operate the Vail/Cartridge Washing and Tunnel 3. Having Knowledge in Aseptic Operation 4. Operate the Autoclave 5. Knowledge in Equipment preparation. Desired Candidate Profile Must have worked in Sterile injectable Plant. Interested Applicant can send their CV on janhavi.shedekar@mjbiopharm.com or contact on 9619744167.

1. Water sampling and testing 2. Media preparation and sterilization 3. Handling of microbiology lab instruments (pH meter, Analytical balance, Autoclave, Laminar air flow, and Incubator) 4. Testing of Food and Masala samples. 5. General knowledge of log book and Good Laboratory Practice norms. Role & responsibilities Interested candidates can share their Resume on WhatsApp - 8905997178

Dear Aspirant , Greetings From Eugia Pharma Specialties , Unit ..! We glad to inform you all that we planned Walk In Interviews for below vacancies in our Manufacturing unit. Department - Production (Injectable) Qualification - M. Pharmacy / B. Pharmacy / M. Sc /B Sc / Diploma / ITI Designation - Sr. Executive / Executive/ Operators Experience - 2Yrs to 8 yr. Skills - Vial Filling/ Sealing / Autoclave / Lyo and etc Work Location : Eugia Unit -3, Pashamylaram Walk In Details: Date : 23.03.2025 Time : 10 AM - 02 PM Venue : Eugia SEZ (Aurobindo Pharma Limited-Unit 16), Balanagar, Ambatapur, Telangana 509202 Google Maps: https://maps.app.goo.gl/KxN3JSa7wL8MoYpm6 Contact : Mr Prabhakar / Ms Rama

Dear Aspirant , Greetings From Eugia Pharma Specialties , Unit ..! We glad to inform you all that we planned Walk In Interviews for below vacancies in our Manufacturing unit. Department - Production (Injectable) Qualification - M. Pharmacy / B. Pharmacy / M. Sc /B Sc / Diploma / ITI Designation - Sr. Executive / Executive/ Operators Experience - 2Yrs to 8 yr. Skills - Vial Filling/ Sealing / Autoclave / Lyo and etc Walk In Details: Date : 23.03.2025 Time : 10 AM - 02 PM Venue : Eugia SEZ (Aurobindo Pharma Limited-Unit 16), Balanagar, Ambatapur, Telangana 509202 Google link : https://maps.app.goo.gl/TpvUmrAjTBXakHv77 Contact : Mr Prabhakar / Ms Rama

Purpose of the role: Responsible for all areas of the Engineering function of DS block and Water System. Primary Responsibility: Strategic: • To conduct Periodical plant energy audits to improve the efficiency of the system & to bring down the operating cost. • Plant upgradation works planning, execution on periodical basis. • Plan & work towards the target set by the management based on business needs. • Updated & aware of cGMP requirements. Operational: • Operation & Maintenance of Utility equipment’s – Boiler, Chiller, Hot water system, Cooling tower, Air compressor, Pumps, Valves, Piping system. • Operation & maintenance of clean Utility equipment’s: Raw water storage & Distribution system, Water Pre- Treatment system, Softener, Purified water generation, Water for Injection generation, Pure steam generation along with Storage & Distribution system. • Attend to Preventive & Breakdown maintenance for Plant & Process equipment’s related to Drug product- Filling lines, Autoclaves, Manufacturing/ Filtration vessels, CIP, SIP, TCU, Autoclaves, Packing machine, etc. Drug Substance- Fermenters, Centrifuges, Homogenizers, HPLC columns, Filtration vessels, CIP, SIP, TCU, Autoclaves, etc. • Gas distribution systems. • Mechanical maintenance support Fire protection systems. • Mechanical support for ETP & STP. • HVAC, BMS, EMS systems. • Good Documentation practices. • Monitoring of outsource agency for plant operation. Review & coordinate for finalization of agreements. • Preparation/Review/Training of SOP, Preventive Maintenance, Break down Maintenance, Schedule, Planning. • Knowledge of plant safety & cGMP requirements. Audit & Statutory Compliance. • Coordination with user departments & plan for Preventive/Breakdown maintenance. • Ensure smooth operation of plant & machinery to avoid breakdowns & production loss. • Plan for required spare parts inventory & AMC. • Shift scheduling, Manpower planning & reporting. • Computer skills including Auto CAD, Microsoft Projects. • Prepare/ Review/ Execution of SLIA, URS, DQ, QRM, CLIA, FAT, SAT, IQ, OQ & Support for PQ. • Goal settings to team members & annual review. Providing the same to department head for review & approval. • Responsible for handling of controlled documents such as SOP’s, logbook and qualification protocol etc., • Responsible to ensure preventive maintenance of the equipment is completed as per schedule and review the preventive maintenance schedule as per SOP. • Prepare/ Review/ Execution of SLIA, URS, DQ, QRM, CLIA, FAT, SAT, IQ, OQ & Support for PQ including EDMS documentation

Pfizer Healthcare India Private Limited - Visakhapatnam Walk - in interviews for Freshers Junior Associates - Manufacturing Dates & Venue: Written Assessment & Personal interview on Wednesday, 26th Mar 2025 at 9:00 AM Interview address : Government Polytechnic College, Pharmacy Block, Kancharapalem, Visakhapatnam - 530007 Eligibility Criteria: Diploma Pharmacy only (2024 Pass out) & Pass Percentage 60% in Academic & No backlogs. Job Description Operate production equipment such as injectable machines, sterile machines, parenteral machines, formulation machines, filling machines, capping machines, compounding machines, washing machines, sealing machines, Visual inspection & packing machines. Monitor and control the production process to ensure quality products are produced within specified parameters. Maintain accurate records of production data and perform routine maintenance tasks on equipment as required. Collaborate with other team members to resolve issues and improve overall efficiency. Ensure adherence to Good Manufacturing Practices (GMP) guidelines.

Role & responsibilities Drug Product (Filling-Officer/Executive) Experienced in handling of O-RABS, Operation of Vial washing/Filling/Lyophilizers/Autoclave/Process vessels. Bacterial vaccine manufacturing- (Upstream/Downstream) Experience in execution of upstream process & of Downstream purification operations

Formulation and Preparation Execute the preparation of formulations as per predefined recipes and batch records. Measure and mix ingredients accurately to meet quality standards. Monitor critical process parameters such as temperature, pressure, and mixing speeds. Autoclaving Operations Operate and monitor autoclaves to sterilize equipment, materials, and products. Ensure proper loading and unloading of materials into autoclaves. Maintain autoclave logs and verify cycle parameters to meet sterilization requirements. Filling Operations Operate and maintain filling equipment for liquid, powder, or other formulations. Ensure accurate filling of products into containers, maintaining precision and adherence to specified quantities. Conduct routine checks for leaks, spills, or defects during filling. Vial Washing Operate automated/semi-automated vial washing machines. Conduct inspections to ensure vials are free of particulate matter and meet cleanliness standards. Document washing activities and perform regular cleaning of equipment. Sealing and Capping Operate and monitor vial sealing and capping equipment to ensure proper closure. Conduct in-process checks for sealing and capping integrity. Troubleshoot minor issues with sealing and capping machines to minimize downtime. Compliance and Documentation Follow Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs), and safety guidelines. Complete batch production records, equipment logs, and other documentation accurately and promptly. Assist in internal and external audits by providing necessary production documentation. Maintenance of Equipment Ensure all equipment is cleaned, maintained, and ready for use according to SOPs. Conduct minor preventive maintenance and assist the maintenance team in troubleshooting issues. Maintain cleanliness and organization in the production area. Experience : 3 to 7 Years Work Location : Hyderabad, Qualification: ITI, Diploma / B Tech (Mech, ECE, EEE), Graduation, Post Graduation

Location : Rajpura City : Rajpura State : Punjab (IN-PB) Country : India (IN) Requisition Number : 37640 Business Title: Technician Production Effective Global Job Title: Technician Production Reports to : AM (Production) Role Purpose Statement : Responsible for performing various tasks to operate, monitor, troubleshoot, perform preventive maintenance, safety, food safety, chemical safety and GMP etc Main Accountabilities : Operate churn cum blending of VP refinery & RO refinery in accordance with established procedure and guidelines Operate short mix, bleacher, autoclave, deo, Fractionation, and acid oil plant in accordance with established procedure and guidelines Perform necessary pre-operation activities to ensure proper equipment startup and Operations Monitor plant parameters to ensure quality production and reduce unplanned stoppages and maintain log-books of the same Responsible for upkeeping & cleanliness of Churn and blending section and to maintain 5S of surrounding areas Supervision/monitoring of work of contractual manpower deployed in the churn and blending & to guide them as and when required Responsible for maintaining quality parameters and avoid/control wastage within standards provided To actively participate in workshops, trainings organized from time to time and demonstrate the learnings at shopfloor Knowledge and Technical Competencies : Knowledge to operate, maintain (Maintenance) & trouble shooting of refinery operations Manpower handling Education/Experience : Full time Diploma in Mechanical or Electrical Five yearsexperience in edible oil or FMCG Manufacturing Industry Bunge (NYSE: BG) is a world leader in sourcing, processing and supplying oilseed and grain products and ingredients Founded in 1818, Bunges expansive network feeds and fuels a growing world, creating sustainable products and opportunities for more than 70,000 farmers and the consumers they serve across the globe The company is headquartered in St Louis, Missouri and has 25,000 employees worldwide who stand behind more than 350 port terminals, oilseed processing plants, grain facilities, and food and ingredient production and packaging facilities around the world Bunge is an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, transgender status, national origin, citizenship, age, disability or military or veteran status, or any other legally protected status Bunge is an Equal Opportunity Employer Minorities / Women / Veterans / Disabled

Roles and Responsibilities Operate production equipment such as autoclaves, blister packers, bottling machines, capsule fillers, granulators, lyo (lyophilization) machines, ointment makers, osd machines (osd-general & osd-beta), vial washers & tunnel dryers. Ensure quality control measures are in place to maintain high-quality products. Collaborate with team members to achieve production targets efficiently. Maintain accurate records of production processes and results. Participate in continuous improvement initiatives to enhance productivity.

Role & responsibilities oHandle critical raw material without anyissues. o Handle hazardous solvent and dangerous chemicals with zero accident andsafely. Plant batch monitoring and data analysis forimprovement. Handle Autoclave to 28-30 kg pressure, ANFD Filtration, Distillation Reactor,scrubbe. To planning and carry out all production activities in shift as per productiontarget. Maintaining production and raw materialrecords. Handle H2So4, Solvents,Citric Acid,H2S Gas. Handle Scrubber System. HandlingCentrifuge ,GLR,SSR,Spray Dryer,FBD, Milling. Handle PLC System Handle Multi product ,BMR,LOGBOOK Interested candidate share resume at 9120534834/shahala.bano@teamlease.com Preferred candidate profile Perks and benefits

Role & responsibilities 1. Follow the instruction & procedure given in Entry- Exit SOP (Standard Operating Procedure) of Grade C, decartoning area and Grade B’ area. 2. Responsible a procedure for proper functioning or behaviour in aseptic area. 3. Follow the personnel hygiene practices in factory premises. 4. Follow the GMP (Good Manufacturing Practices) and GDP (Good Documentation Practices) as per given in SOP. 5. Responsible for monitoring of temperature, relative humidity and differential pressure. 6. Responsible for monitoring of differential pressure of laminar air flow units and pass boxes. 7. Responsible for handling of material movement in production area. 8. Responsible for maintain the document as per GDP and area as per cGMP. 9. Responsible for to maintain day to day records. 10. Responsible for training to new joining chemist, workers and operators for their respective job. 11. Carrying out the line clearance before starting the operation. 12. Responsible for planning of manufacturing as per availability of RM and PM. 13. Responsible for supervision of preparation and filtration of cleaning/ disinfectant solutions and fogging solutions. 14. Responsible for supervision of equipments/ machines and utility readyness before batch manufacturing. 15.Responsible for supervision of operation and cleaning of steam sterilizer, compounding vessel and holding vessel, vial washing machine, sterilization and depyrogenation tunnel, washing and drying and wrapping of garments and pass box and laminar air flow. 16. Responsible for supervision of handling of filters, filter integrity testing apparatus, silicon tubing, decartoning area and hose pipes and cleaning and wrapping of glassware, auxiliary items and machine parts. 17. Responsible for supervision of operation of pH meter and stirrer. 18. Responsible for supervision of aseptic process stimulation, post media fill cleaning and sanitization of machine and area as per procedure. 19. Responsible for destruction of media filled vials. 20. Responsible for supervision for general area cleaning and sanitization of grade ‘C’ and ‘D’ area and fogging activity of respective area. 21. Responsible for verification of load cell. 22. Responsible for verifying the handling of waste generated in production area. 23. Responsible for non viable particle count (online and offline) monitoring. 24. Recording the operation and cleaning details in batch manufacturing record and equipment uses log book. 25. Responsible for handling of equipment like homogenizer, rota evaporator, magnetic stirrer, ultrsonicator, pH meter and fogger. 26. Follow the procedure for dispensing room and responsible for RM and PPM dispensing and additional materials issuance. 27. Responsible for all data entry for batch manufacturing process in pharmacloud system. 28. Responsible for audit preparation and execution. 29.To undergo periodic medical checkup arranged by the company. 30.Performing the task assigned by the supervisor. 31. Reporting regarding unsafe act/ unsafe condition/ accident/ incident to supervisors. Preferred candidate profile Candidate Should have Exposure of Pharma Injectable Plant. Candidate Should well familiar with Pharma Guidelines. Candidate should have good Verbal and Written Communication Willing to Relocate in Navsari, Gujarat, Willing to Work in a Shift.

Greetings from Pulse HR Consultants! We are having urgent openings in the leading Injectable Pharma Industry at Hyderabad location for the below positions Production Department. 1. Technical Assistant / Sr. Technical Assistant -Production injectables Diploma/ B.Sc. with 2 to 9 years Compounding, vial wash/filling, Autoclave, Washing, Filling, Sealing, Batch Manufacturing, Lyophilization Operation, PFS , Ophthalmic 3 piece, BFS & Infusion BAG filling operations. 2. Executive /Sr. Executive-Production Injectables B.Pharma with 2 to 8 years experience in Autoclave, Washing, Filling, Sealing, Batch Manufacturing, Lyophilization Operation, PFS , Ophthalmic 3 piece, BFS & Infusion BAG filling operations. Please share and refer to info@pulsehr.org / pavani@pulsehr.org