53 Vial Washing Jobs

Hi, Greetings from Adecco , A Leading Manpower Consulting Company!!! We have been retained by Leading Pharmaceuticals Company in Ahmedabad for their Manpower Requirements. We have an following Openings as of now. 1) Operators 2) Technician 3) Aseptic Operator 4) Aseptic Officer Education: ITI/Diploma/Bsc/Msc/B Pharma / M Pharma Experience: 3 to 10 Years. Interested candidates please connect on below contact details. Mayuri Shah Senior Consultant (Life Sciences & Pharmaceutical) Mail id : mayuri.shah@adecco.com M-(whatsapp) 7984968546/ 9714846221 Adecco Group India

Role & responsibilities Role - Aseptic Area Manufacturing Skill operation and supervising of filling machine, sealing machine , ALUS operation , storage vessel operation and cleaning Qualification B. Pharm/M. Pharm Category – Staff

You will be responsible for handling production equipment including vial washing & Depyrogenation tunnel, Autoclave, Manufacturing, Steam air sterilizer, Laundry area, Vial coding (Domino), and external vial washing. Additionally, you will be in charge of the requalification/qualification of equipment such as autoclave, vial washing, and tunnel. Your duties will also include managing the auto CIP & SIP process of manufacturing tanks, as well as having knowledge about audit trails and data backup. Familiarity with computer systems like eBMR, PLC, and SCADA will be essential for this role. Furthermore, you should possess knowledge about change control, regulatory affairs, corrective and preventive actions (CAPA), and environment, health, and safety (EHS) activities. The ideal candidate will have a Bachelor's or Master's degree in Pharmacy, along with 4 to 8 years of experience in the field. Previous experience at Zydus for 12 to 24 months is preferred. This position is based in the Production Department at Zydus Pfizer in Ahmedabad.,

Operate and clean HPHV steam sterilizer, vial washing machine, and depyrogenation tunnel. Prepare machine parts and load patterns for production use. Wash and prepare garments for manufacturing areas. Prepare and filter disinfectants, IPA, and other cleaning agents. Perform equipment and room cleaning in processing areas as per SOPs. Execute batch documents and maintain related logbooks online. Handle various types of filters and conduct filter integrity testing. Participate in equipment qualification processes (DQ, IQ, OQ, PQ). Execute production activities and achieve finished product (FP) targets while complying with cGMP standards. Follow cleaning procedures and accurately log data. Maintain daily operations in manufacturing areas. Report all activities, deviations, and problems to the reporting officer. Attend and follow regular training programs related to the role.

Experience in Sterile injectable, specifically in vial washing and tunnel areas Sound knowledge of cGMP, aseptic operations, and production documentation. communication and team coordination. Maintain production documentation and logbooks accurately.

Interview for SVP & Injectable Pharma Formulation Plant in Bharuch on Company / Permanent Payroll Experience: 2 to 6 Yrs CTC: As per industry Work Location: Dahej Send CV on sdpbharuch@gmail.com with Subject: SVP Bharuch & Call 7600033423 Free Job Required Candidate profile Autoclave Operator Granulation Operator Mixing Operator Grinding Operator Cartonator Operator Washing Tunnel Operator Ampoule Filling Operator Vial Filling Operator Vial Sealing Operator Lyo Operator

Interview for SVP & Injectible Pharma Formulation Plant in Bharuch on Company / Permanent Payroll Experience: 2 to 6 Yrs CTC: As per industry Work Location: Dahej Send CV on sdpbharuch@gmail.com with Subject: SVP Bharuch & Call 7600033423 Free Job Required Candidate profile Autoclave Operator Granulation Operator Mixing Operator Grinding Operator Cartonator Operator Washing Tunnel Operator Ampoule Filling Operator Vial Filling Operator Vial Sealing Operator Lyo Operator

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.

Role & responsibilities : 1 Execution of Process equipment IQ and OQ 2 Maintenance and changeover of Vial washing, Tunnel, filling and capping machine 3 Operation and maintenance of Lyo 4 Responsible for shift maintenance 5 Maintenance of Autoclaves, DHS, Process vessels 6 Responsible for execution of preventive maintenance activities as per schedules and checklist 7 Responsible for handling the process equipment breakdown activities to minimize the equipment down time. 8 Record and maintaining of preventive maintenance logbooks and schedules as per cGMP 9 Responsible for spare parts availability. 10 Ensure the safety at workplace. Preferred candidate profile: Qualification: ITI/Diploma (Mechanical)

1. Instrument Decontamination: Receive used medical instruments and equipment from various hospital departments and decontaminate them using mechanical cleaners, ultrasonic machines, or manual cleaning as appropriate. 2. Sorting and Inspection: Sort, inspect and disassemble contaminated instruments, checking for damage or wear and ensuring that they are suitable for sterilization. 3. Sterilization: Operate and monitor sterilization equipment such as autoclaves and ethylene oxide (EtO) chambers, following established procedures to ensure the instruments are properly sterilized. 4. Packaging: Properly package sterilized instruments and equipment, ensuring that they remain sterile during storage and transport. 5. Inventory Management: Maintain an accurate inventory of instruments and equipment, including tracking expiration dates for sterilization supplies. 6. Quality Control: Perform routine tests and checks to verify the effectiveness of sterilization processes and ensure compliance with established standards. 7. Documentation: Maintain detailed records of instrument processing, sterilization cycles and quality control checks. Document any issues or incidents. 8. Equipment Maintenance: Ensure that sterilization equipment is properly maintained and report any malfunctions or maintenance needs to the appropriate department. 9. Safety and Infection Control: Adhere to strict infection control practices and safety protocols to protect patients and healthcare staff from exposure to infectious agents. 10. Collaboration: Work closely with other hospital departments, including surgery, nursing and clinics, to meet their instrument and equipment needs. 11. Continuing Education: Stay updated on the latest advances in sterilization techniques, equipment and infection control practices. 12. Emergency Response: Be prepared to Handle instrument recalls and investigate any infection outbreaks related to contaminated instruments. Role & responsibilities Qualification HSC/ Any Graduate - Dip in CSSD Preferred candidate profile

Experience: 2 to 10 years of sterile area / injectables Manufacturing experience in a reputed organization Technical knowledge: -Good Technical knowledge in oRABS-Vial filling line and practical experience in handling the injectables manufacturing Equipment. -Worked in USFDA and EMA regulatory approved companies -Excellent quality oriented and result oriented attitude -Good experience in cGMP and GDP

Greetings from Adecco , A Leading Manpower Consulting Company!!! We have been retained by Leading Pharmaceuticals Company in Ahmedabad for their Manpower Requirements. We have an following Openings as of now. 1) Vial Washing Operator 2) Filling Machine Operator 3) Aseptic Operator 4) Autoclave Education: ITI/Diploma Experience: 3 to 10 Years. Interested candidates please connect on below contact details.

Greetings from Kashiv Biosciences!!! We are looking for Process Equipment Engineer for our Biosimilar Manufacturing Plant Based out of Ahmedabad. Below are the further details. Experience 15 - 20 Years of Process Equipment Maintenance Education: B.E/ B. Tech( Mechanical/ Electrical/ Electronics/ Instrumentation) Roles & Responsibilities Responsible for the Plant Maintenance activity of DS (Drug Substance) section equipment's such as Fermenters, Process vessels, CIP vessels, batch centrifuges, TFF systems, Merck chromatography columns, Filter press . Responsible for the Plant Maintenance activity of DP (Drug Product) section equipment's Such as Vial Washing machine, Vial filling & Cap sealing machine, Laminar Air Flows, DPBs, Autoclave, Labelling machine etc. Responsible for Maintaining of biologics MFG units (Cell Culture), Filling Facility (DP),QC,WH and R&D facility . Maintenance of Biologics manufacturing facility (Mammalian) including Development and QC lab(Microbiology). Responsible for QMS Documentation validation and new Equipment Qualification. Required Instruments Exposure : Bioreactor Fermenter Media, Buffer & CIP vessel Continuous Centrifuge Continues Kill system Homogenizer Chrome system TFF system Autoclave Chromatography Candidate Details: The candidate should be from Biopharma industry having exposure Drug Substance and Drug product Maintenance. The candidate should have exposure to regulatory Audits. The candidate should be aware of GDP/ GMP Process. The candidate should have exposure to new equipment qualification & QMS as well . The candidate should have good communication skills. Interested candidate please share the resume on my mail id manan.hathi@kashivindia.com Regards HR Team Kashiv Biosciences

Role & responsibilities For operator / Technician Role - Aseptic Area Manufacturing Skill - Operation of filling machine, sealing machine , ALUS operation , storage vessel operation and cleaning Qualification Diploma Eng/ITI Category Operator Thanks & Regards Renu Kumari Senior Consultant (Life Sciences & Pharmaceutical) Email : renu.kumari@adecco.com M-(whatsapp) : 6364920532 Adecco Group India

Formulation/ Vaccine/ Sterile Drug Product Manufacturing Qualification requirement: M.Sc/B.Sc (Life Science) B.Pharm/M.Pharm Diploma / ITI (Experience in aseptic operation) Fresher's & Experienced (1 5 Years) Formulation Filling (Vials , BFS, PFS) Vial Washing, Depyrogenation Sealing & Capping Sterile aseptic operation C- Rabs, O-Rabs, Isolator Autoclave operation SOP/BMR/QMS

-Operation of Vial/Ampoule washing machine -BMR -Classified area monitoring -validation of the machine Interested candidates can share resume on dipika.parmar@milanlabs.com

Manager - Processing (Production) Role: We are seeking a dynamic and seasoned individual responsible for overseeing day-to-day processing operations in sterile manufacturing, ensuring alignment with production schedules and regulatory standards. The role focuses on identifying process inefficiencies, leading improvement and automation projects, and collaborating with cross-functional teams to drive productivity, reduce waste, and enhance product quality. This position demands strong technical knowledge of sterile processing equipment and a proactive approach to maintaining seamless production workflows and continuous operational improvements. Location: Umarsadi (Vapi, Gujarat) Main Tasks: Manage and oversee work orders for our product lines, ensuring efficient execution of production plans to maximize machine performance. Plan and implement batch production on a product-specific basis, optimizing throughput and minimizing downtime. Collaborate with cross-functional departments to ensure uninterrupted operations and timely execution of preventive maintenance schedules. Lead initiatives to reduce market complaints, aiming to maintain a production ratio of over 20 million units per justified complaint. Review BMR for new products to be processed on syringe lines. Review and approve BMRs for new products prior to processing and verify completed BMRs for submission to Quality Assurance. Develop, review, and implement SOPs for syringe processing operations, ensuring thorough training and compliance among line operators. Monitor and enhance line yield while working to minimize rejection rates through process improvements and quality control measures. Ensure timely preparation of customer samples as per specifications, with accurate documentation in BMRs and logbooks. Oversee SAP activities related to batch processing, including data entry, reconciliation, and return of unused materials to inventory.. Ensure optimal shift-wise performance of SPRC machines, maintaining complete and accurate documentation in SAP, BMRs, and logbooks. Prioritize and coordinate the ETO process of completed batches, ensuring all related entries are updated in both BMRs and SAP. Maintain audit readiness by ensuring no critical observations in the production area through strict compliance and monitoring. Ensure NVPC records are correctly attached to the respective BMRs and submitted to QA within the designated timeline. Lead training programs for staff and operators on cleanroom protocols and enforce adherence to cGMP standards. Ensure full compliance with the most recent EHS guidelines across all production activities. Drive continuous improvement of the EHS management system through effective implementation, monitoring, and periodic review. Requirement: M.Pharm /B.Pharm /B.Sc /M.sc / BE (Chemical, Electrical, Instrumentation, Mechanical) from an accredited institution. Experience: Proven record of 12+ years in Junior Management in any Pharmaceutical industry with relevant experience in the area of Process Engineering. Competencies: Strong organizational skills and attention to detail. In-depth knowledge of sterile processing equipment: Washing Systems, Depyrogenation Tunnels, Sterilizers, Siliconization Systems. Sound understanding of cGMP, GEP, FDA/ regulatory requirements, and cleanroom operations. Strong command over lean manufacturing, root cause analysis, CAPA, and risk assessment tools. Strong leadership with proven ability to motivate and guide cross-functional teams. Skills: Proficiency in local languages and English, both written and spoken, to facilitate effective communication with employees and stakeholders. Knowledge of SAP, MS Excel, PowerPoint, etc. Strong learning agility and continuous improvement mindset. Contact: careers.hr@schott-poonawalla.com

Role & responsibilities : Supervise sterile manufacturing processes such as compounding, filtration, filling, and sealing of injectable products. Ensure compliance with cGMP, FDA, and other regulatory requirements in all production activities. Monitor and control environmental conditions in aseptic areas, ensuring cleanroom discipline is maintained. Coordinate with quality control, quality assurance, and engineering departments for production-related activities. Review and maintain batch manufacturing records (BMR), logbooks, and other relevant documentation. Perform in-process checks and ensure timely reporting of deviations and non-conformances. Assist in validation activities including media fill, equipment qualification, and process validation. Train and guide production staff on aseptic techniques, gowning procedures, and SOP adherence. Ensure timely availability of materials, equipment, and manpower for smooth production operations. Participate in internal and external audits and support compliance initiatives. Preferred candidate profile Education: B.Pharmacy/ M.Sc. Experience: 1-7 years in injectable (sterile) production in a pharmaceutical company. Knowledge of aseptic processing and cleanroom protocols. Familiarity with equipment like autoclaves, vial washers, filling lines, lyophilizers, and isolators. Understanding of documentation and regulatory requirements (e.g., USFDA, EU GMP, WHO GMP).

Role & responsibilities For Production : Having Injectable Experience of Shop floor activities like Filling, Sealing, Stoppering, Garment Washing Machine, Vial Washing, Autoclave, Ophthalmic, Suspensions (Handling of Homogenizer, Netzsch Mill/Bead Mill and Single use Systems) filtration, Lyophilizes. Having Injectable Experience of Shop floor supervising activities like Filling, Sealing, Stoppering, Garment Washing Machine, Vial Washing, Autoclave, Ophthalmic, Suspensions (Handling of Homogenizer, Netzsch Mill/Bead Mill and Single use Systems) filtration, Lyophilizes. Operations and Training and QMS. For Quality Assurance : Having Injectable Experience of QMS, Audit & Compliance, IPQA, AQA (Microbiology), CSV Validations

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.

Only from Pharmaceutical - Injectables candidate required Role & responsibilities Operation of filling machine, sealing machine , ALUS operation , storage vessel operation and cleaning Experience of operating Glass Vial filling machine / Autoclave / Sealing machine Interested candidates can apply on " hemin.darji@adecco.com" or call on 7567844566

Job description: Hiring Now Production (Formulation & Filling) Hyderabad Bharat Biotech International Limited is looking for experienced professionals for the following roles: Department: Production Roles: Vial Washing, Vial Filling, Autoclave Operation, Compounding & Batch Manufacturing Experience: 3 to 8 Years Qualification: ITI / Diploma / B.Sc Location: Hyderabad Role & responsibilities Operate and maintain vial washing, vial filling, and autoclave equipment. Perform batch compounding and solution preparation as per production schedule. Monitor batch manufacturing activities in compliance with GMP. Conduct in-process checks and ensure cleanliness of equipment and area. Maintain batch records and equipment logbooks accurately. Troubleshoot minor equipment issues and escalate when required. Follow safety protocols and SOPs throughout the operations. Coordinate with QA and other departments for smooth production flow. Interested candidates can share their CVs to "rajiv5653@bharatbiotech.com" Kindly mention Subject Line: " Application for Production Department". Regards, Rajiv Pradhan HR Department

Hi, Greetings from Adecco , A Leading Manpower Consulting Company!!! We have been retained by Leading Pharmaceuticals Company in Ahmedabad for their Manpower Requirements. We have an following Openings as of now. 1) Blister Operator 2) Blister Officer 3) Aseptic Operator 4) Aseptic Officer Education: ITI/Diploma/Bsc/Msc/B Pharma / M Pharma Experience: 3 to 10 Years. Interested candidates please connect on below contact details. Mayuri Shah Senior Consultant (Life Sciences & Pharmaceutical) M-(whatsapp) 7984968546/ 9714846221 Adecco Group India

Walk-in @ GOA We are hiring multiple positions for our manufacturing facility at AHMEDABAD as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Engineering (Instrumentation / QMS / Process Equipment maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification BE / B Tech with relevant functional experience in Calibration / Instrumentation / QMS activities QUALITY ASSURANCE QMS / Documentation / Validation and Qualification / Market Compliance / IPQA - (injectables) (Officer / Senior Officer / Executive/Senior Executive) Experience - 02 to 09 Years Qualification - B. Pharmacy/ M Pharmacy / M.Sc. QUALITY CONTROL (Officer / Senior Officer/ Executive) Experience - 02 to 07 Years Education - B.sc / M.Sc. (Organic Chemistry / Analytical Chemistry) B. Pharmacy / M Pharmacy MICROBIOLOGY (Officer / Senior Officer/ Executive) Experience - 02 to 07 Years Education - B.sc / M. Sc (Microbiology) Injectable Manufacturing (Executive/Senior Officer / Officer / Associate) Experience - 01 to 06 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma with relevant functional experience in injectable manufacturing/ Aseptic area operations/ Visual inspection / QMS activities OSD Manufacturing (Senior Officer / Officer / Associate) Experience - 01 to 05 Years Qualification - B. Pharmacy/ M Pharmacy / Diploma with relevant functional experience in OSD manufacturing and Packing operations / QMS activities Time and Venue : 06th July 2025, 09:30 Hrs to 17:00 Hrs ______________________________________________________ The Fern Kesarval Hotel, Verna Plateau GOA -403710 _____________________________________________________ We would be very happy if you forward or refer any of your colleagues matching the requirement. *Having relevant qualification and experience only can attend the scheduled walk-in.

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 : 29.06.2025 Time : 09 AM - 02 PM Venue : Aurobindo Pharma Limited - Unit - 3 Sy. No. 313, Bachupally, Hyderabad, Telangana 500090 Google Map : https://maps.app.goo.gl/qoL8vZ6EwDm5GcWb8 Contact : Mr Prabhakar / Ms Rama