39 Lyophilization Jobs - Page 2

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

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

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 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

Job Description Company: GreenSignal Bio Pharma Pvt Ltd Location: Gummidipoondi, Chennai, Tamil Nadu Experience: 1-12 years above in production, preferably in the Bio-Pharmaceutical industry, specifically in vaccine manufacturing Educational Qualification: MSc Microbiology/Biotechnology/B. Pharm/B.Tech with more than 8 years of experience in vaccine biologicals and injectables Job Title: Senior Manager / Manager / Executive- Production Job Summary: The Senior Manager /Executive - Production will oversee daily vaccine manufacturing operations, ensure compliance with regulatory guidelines, manage production staff, and drive continuous improvement to enhance operational efficiency and product quality within the pharmaceutical industry. Key Responsibilities: Production Planning and Coordination: Plan, coordinate, and optimize end-to-end vaccine production activities to meet quality standards, timelines, and cost targets while ensuring resource availability. Oversee Manufacturing Operations: Supervise day-to-day manufacturing operations, including formulation, filling, packaging, and storage processes, ensuring efficient workflow and compliance with production protocols. Compliance: Ensure adherence to Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMP), and regulatory guidelines (FDA, EMA, WHO). Issue Resolution: Troubleshoot and resolve production-related issues to minimize downtime and ensure batch integrity. Team Management: Lead and manage production staff, providing training on safety, quality, and operational protocols specific to vaccine manufacturing. Performance Monitoring: Track key production metrics, implement strategies to improve batch yields, and reduce material wastage. Safety Enforcement: Enforce workplace safety protocols to prevent accidents, contamination, and ensure bio-safety compliance. Risk Management: Identify risks in production processes, such as contamination risks or equipment failures, and develop contingency plans. Material Handling: Ensure safe handling, storage, and disposal of biological materials, vaccines, and hazardous chemicals following industry best practices. Process Improvement: Drive continuous improvement initiatives to enhance production efficiency and product quality. Equipment Management: Oversee the maintenance, calibration, and validation of production equipment to ensure optimal performance. Documentation and Reporting: Ensure accurate documentation of production activities and prepare reports for regulatory compliance and internal audits. Skills and Competencies: Strong leadership and team management abilities in vaccine manufacturing environments In-depth knowledge of GMP, regulatory compliance, and vaccine production protocols Proficient in production planning, batch processing, and process optimization Excellent problem-solving and troubleshooting skills within pharmaceutical production settings Strong communication and interpersonal skills for effective team coordination Risk assessment and mitigation capabilities specific to biological production Commitment to bio-safety, product quality, and continuous improvement About GreenSignal Bio Pharma Pvt Ltd: GreenSignal Bio Pharma Pvt Ltd is a leading pharmaceutical company dedicated to delivering quality healthcare solutions, with a strong focus on vaccine manufacturing and biological products. Our commitment to innovation, compliance, and operational excellence drives our success. For more information, please visit our website: www.gsbpl.com How to Apply: Interested candidates can apply at: hr@gsbpl.com Contact us at: 8778926365 Apply Now to join our team and contribute to impactful pharmaceutical and vaccine innovations!

Role & responsibilities: Area- Plant maintenance Injectable/Parenteral/LYO - Handling of Preventive maintenance - Handling of Breakdown maintenance - Having knowledge of Vial Line, LYO & manufacturing skids - SOP/Document preparation and approval - Handling of QMS document Job Location : Baska, near Halol, Dist: Panchmahal, Gujarat

Role & responsibilities Responsible for Drup Product Manufacturing Ensure compliance to Current Good Manufacturing Practices (cGMP)& documentation thereof for various production activities. Filling line in built CIP, SIP operations Knowledge of Isolator VHP, Blending vessels- CIP, SIP Good at QMS Regulatory inspection exposure WHO-PQ, USFDA, EU GMP, TGA,ROW Experience in O RABS, Isolator filling lines Lyophilizers - ALUS, Manual operations Blending of viral, bacterial vaccines Media fill activities , TRS 1044 updates Responsible for preparing production plan in consultation with PPIC department and execution thereof with effective planning and utilization of Men, Materials and Machineries for quality linked productivity. To approve the instructions relating to production operations and to ensure their strict implementation. To ensure that products are produced and stored according to the appropriate documentation in order to obtain the required quality. To ensure that the production records are evaluated and signed by an authorized person. Review investigation of Quality Management System (QMS) including market complaint, Out of Specification (OOS), change controls of manufacturing, risk assessment, Corrective Action and Preventive Action (CAPA) etc. To ensure the qualification and maintenance of department, premises and equipment. Ensure compliance to master formula and process provided in the Batch Manufacturing Record (BMR). To ensure that the appropriate validations are done. Reviewing document like of Standard Operating Procedures (SOPs), Batch Manufacturing Record (BMR), Batch Packing Record (BPR), Master Formula Record (MFR)etc. and compliance reports thereof with training of personnel on the same. Ensure appropriate inventory of Consumable in the Department for smooth functioning. Responsible for Co-ordination with Technical Services, Quality Assurance / Quality Control, Finance, Purchase, Warehouse and Administration Departments for effective management of Production targets. Ensure wastage control and optimization of yield at various stages of manufacturing and packaging operations. Ensure compliance to various In-process control guidelines provided in the batch documents. Ensure periodic preventive maintenance of plant and machineries as per schedule worked out by Engineering for optimum performance. Ensure that personnel follow basic safety guidelines during operations. Responsible for the preparation of training calendar for employees and to ensure that the required initial and continuing training of department personnel is carried out and adapted according to need on cGMP and various operational activities. Responsible for preparation of accurate and timely reports of various production activities showing performance and shortcomings against agreed/planned parameters (monthly presentation, work in progress (WIP) statement yield report, monthly planning, expense budget stationary, housekeeping material, production item &capital budget etc). Preferred candidate profile M.Pharm/ B.Pharm / MSc ; Experience- 18 to 25 years Candidate Must have exposure of regulatory Audits should be willing to relocate with family to ahmedabad

Research Scientist- Biologics @chennai Full Time Qualifications: PhD or MSc in Lifesciences/Biotechnology or related field At least 5-10 years experience in Cell and Tissue manufacturing, including GMP environment. Demonstrated experience in an research and development/manufacturing role is highly required Must Have - Lyophiliser Work Experience Key Responsibilities: Responsible for new product development, scale up of successful R&D batches & transfer of technology to commercial batches Implementation of new product development process. Answering regulatory related queries within lead time Review regular basis stability studies protocol and reports Document preparation (PDR, MFR,PV,Stability) for regulatory dossiers Developing the quality of product with cost effectiveness Training the formulators for literature study before development & conduct patent search Achieving development target of sample product for registration of export samples as well as domestic samples Checking all Project In Process Data, COA & Log books of all project members. Fulfil requirement of MFR, BMR & Tech Transfer Products. Reducing development costs & product cost Resolve trouble shooting in production during scale up and commercial batches Customized sampling for different customer Review process validation and analytical validation protocols and reports Providing information for vendor management approval system Leading the entire department Competencies Required: Aseptic processing techniques. GMP working knowledge. Human tissue and cell handling techniques. Closed loop operations. Cell expansion techniques. Process equipment handling like Biosafety cabinets,Lyophilizer, filling etc. For Faster Response Apply Here - https://forms.gle/bdnTopW6fEA4WFLW8