320 Sterile Jobs - Page 13

Role & responsibilities : Candidate should have experience in Injectable plant (Parenteral) Candidate should have experience in Vial line (Liquid/Lyophilizer), PFS Line, Bag Line, Cartridge line, Ampoule Line. Candidate should have experience in Imported Equipments like Groninger, B+S, Bosch, Pluemat, SFM, Steriline (Vial/PFS/Cartoridge/Bag/Ampoule Lines), IMA/GEA/Tofflon (Lyophilizer), Fedegari (Autoclave), Bonfiglioli (Leak test), Caser (X ray). Candidate should be capable of handling the Team and Block/Plant. Candidate should have experience in HVAC/Water system Candidate should have hold on Documentation line QMS/Qualifications. Candidate should have experience in Energy Conservation pro...

Sterile Operations Trainer Grade: G9 Designation: Senior Manager Location: Halol 1 Job Description: Education: B. Pharm / M. Pharm Overall responsibility of Aseptic Training Academy (ATA), Baska To plan, develop, and execute training at Aseptic Training Academy (ATA) - Sterile Operations for Sun Global Operations (SGO) Training. Creation of simplified training modules for technicians, scheduling and execution of training Creation of training evaluation and/or feedback systems Course creation according to levels (Level 1 - Technicians, Level 2 - Supervisors and above, Level 3 - Managers and above) pertaining to sterile operations Planning, scheduling & execution of technical training program ...

Role & responsibilities Operate and manage freeze drying and lyophilization equipment , including Freeze Dryer, Palltronic Integrity Tester, and CLU. Ensure smooth functioning of computerized systems such as eBMR, PLC, SCADA , and manage data integrity, audit trails, and system backups. Participate in equipment and area qualification/requalification activities, including LAF (Laminar Air Flow) systems. Ensure adherence to and documentation of Change Controls , Risk Assessments (RA) , Corrective and Preventive Actions (CAPA) , and EHS (Environment, Health, and Safety) protocols. Ensure compliance with regulatory standards and assist during audits and inspections . Maintain accurate and timely...

- Sterile Injectables Handling dealing with liquid ampoules, vials, lyophilized products - FIFO / FEFO Implementation - ERP Inventory Management - Inward & Outward Material Management - Warehouse Housekeeping - Pharmaceutical industry - Compliance

- Sterile Injectable Manufacturing (Core) - Liquid ampoules, vials, lyophilized products - BMR/BPR Documentation - cGMP - Production Line Operation - Pharmaceutical Equipment Handling - Cleaning/Sterilization - Internal Audit/Validation - Maintenance

- 8+ yrs in Sterile Injectable Manufacturing - 3+ yrs as Production Manager in Injectable Plant - Handling Liquid Ampoule, Vial, and Lyophilized Vial Lines, BMR/BPR Documentation - Leadership & People Management - cGMP; WHO-GMP; FDA Guidelines, SOP

Must have Exp in Injectable & Parenteral formulations. Lead and optimize end-to-end sterile injectable production, ensuring cGMP compliance, on-time delivery and continuous process improvement.

Company: Leeford Healthcare Ltd. https://www.leeford.in/ https://www.linkedin.com/company/1464125/admin/dashboard/ Role: Production Manager Sterile Prep (Eye/Ear Drops) Experience: Minimum 8-12 years Location: Baddi Education: Graduation; Post Graduation: BSC/B.Pharma Desired Candidate Profile: Required experience of 8-12 years, Exposure to work with one or more reputed organization. Knowledge of Sterile manufacturing like Eye Drops & Ear Drops i.e. Manufacturing, Filling, Sealing and packing of products. Job Description: Designation: Production Manager Sterile Prep (Eye/Ear Drops) Work Profile: 1. Responsible for Batch Manufacturing in SVP line, aqueous line. 2. Responsible for operating of...

Novo Nordisk Global Business Services (GBS) India Department: GCM DP RoW Location Hyderabad, India Are you an experienced aseptic manufacturing project manager with a strong technical background and a passion for making a direct impact on patients'' livesDo you thrive in an international environment where cultural awareness is key to your successIf so, this could be your dream role! ApplyNow! The Position As a Project Manager in Aseptic Manufacturing, you will lead and mentor cross-functional teams, including both Novo Nordisk and our Contract Manufacturing Organisation (CMO) partners. It includes, Ensure the seamless Technology Transfer and manufacturing of our commercial products, always u...

Novo Nordisk Global Business Services (GBS) India Department GCM DP RoW Job Location Hyderabad Are you an expert in aseptic manufacturing with a strong quality mindset and a desire to make a tangible impact on global healthNovo Nordisk is seeking a dedicated Manufacturing Specialist to join our Global Contract Manufacturing Drug Product (GCM DP) team in Hyderabad, India. In this role, you''ll be crucial in ensuring the high-quality production of life-saving insulin and GLP-1 products through our Contract Manufacturing Organizations (CMOs). ! The Position As a Manufacturing Specialist (SME), you''ll be the go-to expert driving Technology Transfer projects for commercial products, ensuring top...

Job Role : Block Head (Engineering) Grade : Senior Manager Location : Guwahati Experience : 15+ Years (experience in lyophilizer ) Qualification : BE. Instrumentation Overseeing the engineering functions of parenteral block. Coordination with production personnel, contractors & machine manufactures to sort out machine related problems, major and minor modifications for smooth running in process. Tracking and maintaining the critical spares required for preventive and routine maintenance Planning various maintenance schedules and lead the team of engineering to ensure implementation of the schedules with the help of junior sub-ordinates for improving the overall reliability of the equipments....

Dear Candidate, We are looking for formulation scientists for our Ophthalmic and Nasal teams in Formulations, focusing on the formulation development of sterile ophthalmic dosage forms solutions, suspensions, and emulsions. This role involves complete ownership of formulation and process development with a strong emphasis on regulatory compliance and timely execution. Position1: Assistant Manager Department: Ophthalmic team - Formulation Development Required Exp : 8-12years Position2: Research Associate/Sr.Research Associate Department: Nasal team - Formulation Development Required Exp: 4-8years(Candidates from injectables background can also apply.) Role & Responsibilities: Formulation & Pr...

Supervise daily production activities of injectable formulations. Ensure compliance with cGMP, safety, and quality standards. Plan and execute production schedules to meet targets Coordinate with QA, QC, Maintenance, and Warehouse teams. Required Candidate profile Lead and train production staff for operational efficiency. Handle documentation: BMRs, SOPs, deviations, and change controls. Support audits – internal, regulatory (USFDA, EU, WHO-GMP).

Hi, We have urgent position open for the Warehouse Executive / Junior Executive role. Responsible for managing the receipt, storage, issuance, and documentation of materials (raw, packaging, and finished goods) in compliance with cGMP, GDP, and company SOPs. Ensures material traceability, cleanliness, and timely supply to production particularly for sterile/injectable operations. Key Responsibilities: 1. Material Handling & Storage 2. Documentation & Compliance 3. Material Issuance 4. Cleanliness & Safety 5. Vendor Coordination & Dispatch (Optional)

Role & responsibilities Working as a Production Chemist. Experience into BMR, BPR. Experience in Sterile, sterilization. Batch Planning, Batch Manufacturing

Responsibilities: Participate in management review meetings. Review of department trend analysis reports and internal studies or investigations. Ensure corrective action is initiated when required. Provide complete analysis of test results, investigation or information studies. Be capable of assuming study director responsibilities for all routine testing as well as certain advanced or specialized studies as requested by clients. Duties may include test scheduling, test preparation, proper application of test method(s), data collection, data review, and approval of final report of analysis. Maintain thorough knowledge and understanding of all SOPs pertaining to microbiology/sterility assuran...

Cleaning, disinfecting, sterilizing, and distributing surgical instruments and medical equipment. Ensures proper functioning of sterilization processes, maintains hygiene standards, and follows infection control protocols.

Job Role: Junior Associate to Senior Associates Manufacturing (Injectables) Eligibility criteria: Qualification: Any Diploma/BSc/B.Pharma/MSc/M.Pharma Years of Experience: 2 to 10 Years should be from injectable manufacturing plant. 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 othe...

*Job Description:* We are seeking a highly motivated and detail-oriented Production Executive specializing in Dry Injection to join our dynamic team. The successful candidate will be responsible for overseeing the manufacturing processes of dry injection products, ensuring compliance with industry regulations, and maintaining high standards of production quality. *Key Responsibilities:* - Oversee daily production activities related to dry injection products and ensure smooth operations in the manufacturing unit. - Ensure adherence to Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs). - Monitor production schedules and adjust as needed to meet targets and deadlines. ...

Qualification: Post-graduate in Pharmacy or Pharmaceutical Engineering Experience: 15 to 20 years in sterile manufacturing plant operations, with a minimum of 10 years in a leadership role and at least 7 years in a regulated sterile manufacturing environment. About The Company Fresenius Kabi Oncology Limited, a wholly owned subsidiary of Fresenius Kabi, is a leading player in the oncology generics market with a broad portfolio that includes injectables, cytotoxic, and APIs. Its state-of-the-art production facility in Baddi features dedicated units for cytotoxic and non-cytotoxic products, including liquid and lyophilized injectables. The facility is approved by global regulatory authorities ...