39 Lyophilization Jobs

For Production : Exposure pertaining to groninger vial filling , groninger bottle filling, fedegari autoclave, NKP vial filling machine, lyophilizer , spray dryer , aseptic process, complex manufacturing, exposure to CIP/SIP, skid manufacturing, pre filling syringe , QMS is required. Experience required is 2-6 yrs. For Engineering : Should to preventive/ breakdowns maintenance of sterile manufacturing plant, maintenance of autoclave, filling machine - vial, bottle, ampoule, ophthalmic, lyophilizer, freeze dryer machine , BFS machine is required. Experience required is 2- 6 yrs. Job Location : Sun Pharmaceutical Medicare Limited : Nr. Hotel Sarvottam, Survey NO 22 & 24 , Village : Ujeti , Post :Baska , Tal: Halol : 389350 Dist. Panchmahal, Gujarat, INDIA. Mb No : 02676 610 603 / 628

Walk In Interview Interview Day & Date : 14-06-2025 (Saturday) Time : 08:00 to 11:00 Am Department : Production Sciences or Pharmacy Graduates (M.Sc. / B. Pharm. / M. Pharm.) with 0 to 6 years Experiences in parenteral manufacturing (vial / ampoules / bottles of glass or Plastic through BFS technology). Candidate worked in production compliances / remediation / and having experiences of managing quality system document (CCN / CAPA / investigation etc.) ACULIFE HEALTHCARE PRIVATE LIMITED. Formally known as nirlife Near Railway Crossing (Sanand - Viramgam Highway) Village: Sachana, Taluka : Viramgam District: Ahmedabad 382 150

Role & responsibilities To maintain a clean and sterile OT. To clean and pack the instruments and autoclave and provide enough sets and linen. To maintain the autoclave-machine and eto machine. To pack and autoclave sufficient dressing sets, other set’s like bone-marrow, ICD etc. For use in the floors. To help in cleaning and fumigation of the OT. To dispatch the specimen as and when required. To see that all hospital policies are followed. Preferred candidate profile Immediate Joiners will be preferred.

Amneal is coming in your city Hyderabad this 07th & 08th Jun 2025 for Walk In Drive Hiring for Projects & Engineering and Peptide expereince : Walk-In Interview Drive #Hyderabad We are coming to your city for a walk-in interview drive! If you're looking to build a rewarding career with a growing Global Pharmaceutical Company, dont miss this opportunity. Day 1: Saturday, 07th June 2025 Time: 9:00 AM to 5:00 PM Venue: Lemon Tree Premier Plot No. 2, Survey No. 64, HITEC City, Madhapur, Hyderabad 500081, Telangana Day 2: Sunday, 08th June 2025 Time: 9:00 AM to 5:00 PM Venue: Vivanta Hyderabad, Begumpet 1-10-147 & 148, Mayuri Marg, Begumpet, Hyderabad 500016, Telangana Opening in Engineering Department for the following opening : Designation : Sr Executive / Manager Yrs of Exp : 5-12 Yrs Qualification : M.Tech / B.E Expereince into Electrical : Experienced in electrical project execution, compliance, and commissioning, with strong knowledge of HT and LT electrical systems and a solid understanding of pharmaceutical equipment requirements. Expereince into Instrumentation Skilled in automation and instrumentation of equipment and utility systems, with hands-on experience in regulatory compliance, calibration, temperature mapping, and thermal validation. Expereince into Civil Civil engineer overseeing site execution, quality assurance, regulatory compliance, cross-functional coordination, and project documentation in pharmaceutical projects. Expereince into Mechanical Mechanical project scope includes HVAC systems, utility services, regulatory compliance, project timelines, and cross-functional coordination. In-depth knowledge of process equipment used in injectable pharmaceutical plants experience in the installation, commissioning, and qualification of water systems. Expereince into Process Strong expertise in equipment used for injectable manufacturing, with preferable knowledge of isolator systems. Experienced in the installation, commissioning, qualification, and documentation of process equipment Interested candidates who are unable to attend interview, can share their CV on below mentioned Email Id with subject line Application for Falcon indiacareers@amneal.com

Role & responsibilities Formulation development of Injectable FORMULATION for regulated market, USA and Europe. To carry out product development trials, process optimization trials, scale up trials and exhibit batches at manufacturing plant. Literature search of new products, to conduct pre formulation studies, other studies like Tubing studies, compatibility studies and filter studies. Preparation of development protocols, QbD/Risk assessment documents, technology transfer documents and product development reports. Ability to carry out investigations, troubleshooting exercises related to development, scale up and exhibit batches. Preferred experience on Lyo product and colloidal Iron product development.

Process Mechanical, Process Electrical, HVAC, Water System with WFI Knowledge, Utility Electrical (Chiller, DG, Air compressor, Heat pump, Boiler)

Production : Associate /Senior Associate Qualification : B. Pharmacy / M. Pharmacy Experience : 2 to 6 years Must have Injectable and Regulatory Knowledge in any of these areas: Aseptic processing activity (Vial/PFS), Bulk compounding, sterilization,Vial washing & Depyrogenation,Lyophilization & Terminal sterilization process. Infusion bags processing activities, In-process checks and Line Clearance activities, Handling of shift activities and manpower. Computer Proficiency: TW, Documentum , MES & SAP, GEP

Walk-In Drive Hyderabad | June 1, 2025 Join our growing team at OneSource The new way to CDMO We're hiring for multiple roles across our R&D and Manufacturing facilities in Bengaluru. Walk-In Interview Details: Date: Sunday, June 1, 2025 Time: 9:00 AM 4:00 PM Venue: Oakwood Residence, 115/1, Road No. 2, Financial District, Gachibowli, Hyderabad, Telangana 500032 Open Positions: Process Development Lab (Unit 1, Bommasandra) Research Associate | Sr. Research Associate | Scientist Qualification: B.Tech / M.Tech (Biotechnology) Experience: 2 – 12 years Drug Substance Manufacturing (Unit 2, Doddaballapura) Executive | Sr. Executive Qualification: MSc / B.Tech / M.Tech (Biotech, Microbiology) Experience: 2 – 8 years Drug Product Manufacturing (Unit 2, Doddaballapura) Executive | Sr. Executive | Team Leader Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm Experience: 2 – 12 years in sterile injectables

We are hiring for multiple engineering roles in our Sterile Manufacturing Facility and are looking for skilled professionals in Mechanical and Electrical Maintenance with relevant sterile shop floor experience. The ideal candidates should have hands-on exposure to sterile area equipment, preventive and breakdown maintenance, troubleshooting, and facility upkeep. Qualification : BE / Btech Mechanical /Electrical Experience : 5 -15 yrs Key Responsibilities: Operation and maintenance of vial washing, tunnels, filling & sealing machines, manufacturing vessels Exposure to Lyophilizers and Auto-loading systems (for Executive/Associate roles) Performing Preventive Maintenance, Breakdown Maintenance, and Troubleshooting Knowledge of sterile manufacturing environments and regulatory requirements Conduct breakdown analysis and maintain metrics like MTTR / MTBF Overall facility maintenance responsibility Proficiency in English communication If you or someone you know fits the bill, please share profiles at Kirti.k@viatris.com. Also Kindly share your updated CV along with below details: Current CTC: Expected CTC: Notice Period:

Role & responsibilities To maintain a clean and sterile OT. To clean and pack the instruments and autoclave and provide enough sets and linen. To maintain the autoclave-machine and eto machine. To pack and autoclave sufficient dressing sets, other set’s like bone-marrow, ICD etc. For use in the floors. To help in cleaning and fumigation of the OT. To dispatch the specimen as and when required. To see that all hospital policies are followed. Preferred candidate profile Immediate Joiners will be preferred.

Greetings From SP Accure Labs!!! We are conducting Walk-In Interview for Production Injectables formulation department for Compounding Chemist on 30/05/2025 Friday @ our Shamirpet Plant facility. Roles and Responsibilities Conduct quality control tests on injectable products using techniques such as SIP, CIP, TOFFLON, PFS, ISOLATORS, LYOPHILIZATION. Ensure compliance with cGMP guidelines during production activities. Department - Production Role - Compounding activities like CIP, SIP Mixing & Filling Vessels. Desired Candidate Profile 4-8 years of experience in a similar role with (M.Pharmacy, M.Sc, B.Pharma / B.Sc). Strong understanding of chemistry principles applied to pharmaceuticals. Proficiency in compounding, parenteral production, sterile processing, and lyophilization techniques. Experience working with injectable products including oncology treatments. Thanks & Regards, Archana Reddy Team HR

PRODUCTION - Filling and Blending: Designation : Officer & Senior Officer, Executive, Sr. Executive. Qualification : Diploma / B. Sc/ B. Pharmacy/ M. Sc Experience : 3-10 Years The candidate should possess the following skills: BLENDING: Ability to handle shift plans for formulation Blending activities. Operate and maintain equipment like autoclave, blending vessels. Ability to handle and maintain equipment like autoclave, blending vessels, CIP and SIP skids. FILLING: Ability to handle shift plans for filling activities. Operate and maintain equipment like Vial washing, Tunnel Sterilizer, Filling and Capping, Lyo Filling & lyophilization. PACKING & LABELLING: Ability to handle shift plans for Vial Labelling Machine & VVM dot Machines with Inspection system. Operation of Videojet and Control print Printer for Batch Coding. Operation of Track & Trace System, monitoring of Cold room and Deep freezers temperatures. Interested candidates may walk-in with an updated CV, latest increment letter and the last 3 months.

JOB OPENING FOR INJECTABLES QC CHEMICAL 1. Experience: 6 to 7 years Education: M.Sc/B.Sc/M.Pharma Job Description: 1. Well versed knowledge of QC software (Chromeleon, Labsolution, Taimo etc). 2. Knowledge of QC documentation 3. Knowledge of analytical data review. 2. Experience: 3 to 5 years Education: M.Sc/B.Sc/M.Pharma Job Description: 1. Knowledge of laboratory instrument handling such as HPLC, GC, Autotitrator, UV, FTIR etc. 2. Well versed knowledge of GLP, GDP & Data Integrity PRODUCTION INJECTABLES 1. Lyo-Operator/ Officer Experience: 3 to 5 years Education: B.Pharma//M.Pharma Job Description: 1. Knowledge of Lyophilizer operation & troubleshooting 2. Handling of Automatic loading & unloading system 2. Aseptic Area Operator/Officer Experience: 3 to 5 years Education: B.Pharma//M.Pharma Job Description : 1. Knowledge of media fill & dry powder filing machine operation 2. Knowledge of aseptic area operation QC MICRO Experience: 3 to 5 years Education: B.Pharma//M.Pharma Job Description : 1. Preparation of trend data for water analysis & environment monitoring program. 2.Responsible for performing MLT of Water, Raw material and Bioburden Test of in process sample. 3.BET testing of finished products, raw material and stability sample. 4.Sterility Testing of finished products, raw material and stability sample. If interested, share your updated CV along with the below mentioned details on mail id: preeti.yadav@brookssteriscience.com 1. Current Organization 2. Total Experience: 3. Current Designation: 4. Current CTC: 5. Expected CTC: 6. Notice Period: 7. Availability for Interview: With Regards Team-HRA

"Hiring Event Announcement" MFG Production Operators (ITI): 3 to 8 Experience in Injectable production, filling, dispensing, sterilization, autoclave, batch record review etc., activity MFG Packing Operators ( ITI): 3 to 8 Experience in Injectable packing activity. Date & Time : 31st May 2025 || 09 AM to 3 PM IST Venue : Ahmedabad (Invites will be shared based on your shortlisting) Registration Link copy : https://talentcommunity.baxter.com/flows/manufacturing-packing-operators-31st-may-25-gqengvlfs EEO (Equal Employment Opportunity) This is where Baxter International Inc. is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.

Role & responsibilities Experience: 9-14 years Specialization: Injectable Drug Formulation & Development Key Responsibilities: 1. Formulation Development: Lead the design and optimization of injectable drug formulations, ensuring stability, efficacy, and manufacturability. 2. Pre-Formulation Studies: Conduct compatibility assessments, stability testing, and excipient selection to enhance product quality. 3. Scale-Up & Technology Transfer: Oversee successful scale-up from lab-scale development to pilot and commercial manufacturing, ensuring reproducibility. 4. Sterile Manufacturing Expertise: Manage aspects of sterile formulation processes, including aseptic techniques, lyophilization, and parenteral drug delivery innovations. 5. Regulatory Documentation: Prepare and review CMC documentation for regulatory submissions, ensuring alignment with global health authority requirements (FDA, EMA, etc.). 6. Process Development & Optimization: Implement Quality by Design (QbD) and Design of Experiments (DoE) principles to refine injectable formulation strategies. 7. Cross-Functional Collaboration: Work closely with analytical, manufacturing, and regulatory teams to ensure seamless product development. 8. Troubleshooting & Problem-Solving: Address formulation challenges related to stability, compatibility, and manufacturing scale-up. 9. Innovation in Drug Delivery: Explore novel injectable delivery mechanisms, including depot injections, nanoparticle-based formulations, and biopharmaceuticals. 10. Leadership & Mentorship: Guide junior scientists, fostering innovation and technical excellence in formulation research. Qualifications: PhD/Masters in Pharmaceutical Sciences Extensive experience in sterile injectable formulation development with a strong track record of successful product launches. Expertise in aseptic processing, lyophilization, and excipient compatibility for injectables. Strong knowledge of scale-up processes, technology transfer, and industrial manufacturing practices. Proven ability to develop and optimize parenteral drug formulations, ensuring quality and regulatory compliance. Experience with regulatory pathways, and ANDA submissions. Understanding of bio pharmaceutical characterization for injectable products. Preferred candidate profile Candidate with exp of Pre-Formulation Studies and research Candidate with experience of successful scale-up from lab-scale development to pilot and commercial manufacturing, ensuring reproducibility candidate with Sterile Manufacturing Expertise. candidate with experience in Innovation in Drug Delivery: novel injectable delivery mechanisms, including depot injections, nanoparticle-based formulations, and biopharmaceuticals.

Dear Candidates, Greetings from KEYBIZ DASHBOARDS, We are looking for Production Executive & operators injectables for one of our reputed pharmaceutical client, based at Hyderabad & Vizag location. Please find below openings list. 1. Vial Washing 2. Filling 3. Compounding 4. Lyophilization 5. Autoclave 6. Sealing 7. Monitoring of aseptic area / Environmental \ Media Fill \ Lyophilization operation The above positions we are looking for Hyderabad & Vizag locations, interested please share us updated cv to krishna_veni@mydashboards.in Thanks and Regards Krishnaveni - Dashboards Team HR

Role & responsibilities Expertise in batch manufacturing and preparation related activities. To observe & follow all rules and regulations of the production department. Must be from Parenteral background & exposure to Aseptic vial / Bottle filling process is desirable. To be aware and responsible for achieving quality objective and fulfilling the requirements of applicable quality procedures. Technical exposure and expertise on filling & Autoclave machine. Exposure of USFDA audits. Preferred candidate profile Candidate should have relevant experience in USFDA regulatory approved pharmaceuticals (Preferred 21 CFR compliance) organization. Perks and benefits As Per Company Norms.

Walk In Drive For Production Injectables In Formulation Division @ Kothur Department:- Production Injectables Qualification :- Diploma | ITI | B Tech | B Pharmacy | BSc | MSc | M Pharmacy Experience :- 2 to 8 Years Division :- Formulation Interview Date:-05-04-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- MSNF-V, RK Puram & Unit-II, Kothur Venue Location :- MSN Laboratories Pvt Ltd, Formulation Unit -II, Kothur Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001 MSN Laboratories Pvt Ltd,. Formulation Unit-02, Kothur, Nandigama. Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Alembic Pharmaceuticals is looking for Jr. Executive(Operator) - Manufacturing (Injectable) for our Formulation Unit-3, Karakhadi. Job Criteria: 1-7 years ITI/Diploma qualification Job Responsibility: Perform assembling as per defined procedure. Operate filling machine/ Ophthalmic/ PFS machine. Operate homogenizer. Perform batch filtration activity. Perform aseptic manufacturing activity. To unload steam sterilizer and bio-decontamination chamber in co-ordination with equipment preparation and sterilization area. To take part in area qualification activity. To take part in periodic area requalification activity. Aseptic area equipment qualification, filling machine qualification, media fill process. Interested candidates may share their resumes to " injectable@alembic.co.in "

PRODUCTION - Filling and Blending: Designation : Officer & Senior Officer, Executive, Sr. Executive. Qualification : Diploma / B. Sc/ B. Pharmacy/ M. Sc Experience : 2-8 Years The candidate should possess the following skills: Hands on experience in Operation & Cleaning of Vial Washing machine, Depyrogenation Tunnel, Automatic,Terminal sterilization, Vial Filling and Vial Sealing machine & Automatic PFS filling machine. Hands on experience in Operation & Cleaning Lyophilizers with Auto Loading & Unloading Systems (ALUS). Exposure in Aseptic process activities, Aseptic Techniques, Aseptic filling & sealing activities and Media fill activities. Execution Knowledge on manufacturing and compounding activities. Hands on experience in Documentation activities in shop floor. Planning & Execution of Aseptic Media Fill simulation activities & Execution of Interventions. PACKING & LABELLING: Ability to handle shift plans for Vial Labelling Machine & VVM dot Machines with Inspection system. Operation of Videojet and Control print Printer for Batch Coding. Operation of Track & Trace System, monitoring of Cold room and Deep freezers temperatures. Interested candidates may walk-in with an updated CV, latest increment letter and the last 3 months.

Pfizer Walk-in Drive at Vizag for Manufacturing roles Job Title: Junior/ Assistant Associates Manufacturing (Injectables) Eligibility criteria: Qualification: Any Diploma/ BSc (Full time) Years of Experience: 1 to 6 Years should be from injectable manufacturing plant. Interview date & Time: Sunday, 13th April 2025 at 9:00 AM Venue: Hotel Best Western Ramachandra - Vizag # 8-8-36, GNT Rd, Medical Center, Gajuwaka, Visakhapatnam- 530026 Job Description Operate production equipment such as Injectable , Sterile , Parenteral machines, Vial / Ampoule filling , Capping , Compounding , Washing ,Sealing, Terminal sterilization, Stopper process & Visual inspection. 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. Must have experience with USFDA regulatory environment & process.

Title : Research Associate (Injectable- Lyophilizar ) Job Location: Dholka, Gujarat. Experience required : 2-5 Years Role & responsibilities To prepare BOM for new UID activities with respect to costing of NPDs. Timely development and delivery of allotted formulations and any other assigned project as per agreed timelines and budget. Completion of document preparation and formulation activities to support pre-clinical, clinical supplies and technology transfer, exhibit batch manufacturing of developed product. Development of non-infringing strategies for novel formulations in compliance to regulatory requirements for US, EU, and ROW market. To write Lab note books, stability data compilation and tracking of project progress. Preparation and request of spec for raw material, packaging material, in-process controls and finished product specification. Preparation/review of documents for manufacture exhibit/ commercial batches like master formula card, product specifications, product development report and technology transfer docket and co-ordination with support functional team for timely delivery of projects. Identification of product/Process specific equipments/ machinery and record keeping of usage and maintenance. Ensure compliance of SOPs, GLP, and GDP in product development of group.

1. To review and implement Quality Management System for cGMP compliance at Production SVP plant. 2. To review and approval of BMR, BPR in Caliber BRM software. 3. Handling of Caliber QAMS, DMS, Nichelon 5 CMS, Dynamic, serialization & aggregation. 4. Giving the required training, also responsible for Media fill and GMP compliance. Handling of Quality Risk Management (QRM). 5. Responsible for Job allocation of Production Team. 6. To ensure the GMP at all level in the SVP plant. 7. To review and approval of production documentation for compliance with cGMP requirements. 8. To prepare & review SOPs, Validation Protocols, Master Batch Production Records and other related documents at Production SVP plant. 9. To review Change Control, Incident /Deviations and ensure its closure, within given timeframe as per respective SOP. 10. Review signatory for all SOPs, Master Batch Records, Qualification, Validation, documents of Analytical, APQR and Manufacturing equipment, Specifications, Change Control, OOS investigations and other investigations. 11. To coordinate with warehouse team for ensuring the availability of raw material and packing material. 12. Ensure the execution of Process validation and equipment validation. 13. To review batch production Records, to assure that the batch has been manufactured and tested as per laid down procedure / specification. Deviation if any, are recorded, investigated. 14. To conduct and monitor calibration, qualification, validation and requalification activity at site. 15. To ensure release (approval of rejection) the batch manufactured at site. 16. To review product License Application and support Regulatory department, obtaining the product license from the local Regulatory Authority. 17. To review and submit the data / information to Regulatory Affairs for preparation of DMF/dossiers/application for registration of the product with Regulatory Authority of the countries, intended to market the product. 18. To inform top Management on quality issue (if any). 19. Ensure the compliance with online dispensing, manufacturing, filling, sealing, Visual Inspection and packing activities. 20. To ensure implementation of the CAPA initiated as a result of self-audit, customer, regulatory audit in Production. 21. Participation and monitoring all activities of small volume parenteral (SVP) project in coordination with CFT like QA, QC, Engg and warehouse dept. 22. Review and approval of all documents pertaining to small volume parenteral facility. 23. Responsible for Aseptic behaviour in Aseptic area. Interested candidates can share their resme on dipika.parmar@milanlabs.com

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.

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