133 Lyophilization Jobs

1. Production Operations Plan, execute, and monitor day-to-day injectable manufacturing operations (Liquid / Lyophilized / SVP / LVP). Ensure adherence to batch manufacturing records (BMR) and standard operating procedures (SOPs). Coordinate with Planning, QA, QC, Engineering, and Stores for smooth production activities. Monitor in-process checks and ensure timely completion of batches. Ensure line clearance before starting operations. 2. Compliance & Documentation Ensure compliance with cGMP, WHO, USFDA, EU, MHRA, and other regulatory standards. Review and approve BMR, BPR, and related production documentation. Participate in internal and external audits (regulatory and customer). Initiate ...

Interview for SVP & Injectable Pharma Formulation Plant in Bharuch on Permanent Payroll on 09 Nov, Sunday Exp: 1 to 25 Yrs CTC: As per industry Work Location: Dahej Send CV on sdpbharuch@gmail.com with Subject: SVP Bharuch & Call Free Job Required Candidate profile No of Openings Officer - 30 Senior Officer - 16 Executive - 4 Assistant Manager - 4 Manager - 2 AGM / DGM / GM - 1 Share with Your Colleagues & Seniors Free Job Placement Project Expansion on going

Interview for SVP Formulation Plant in Bharuch on Permanent Payroll on 09-11 Experience: 1 to 15 Yrs Work Location: Dahej Apply on sdpbharuch@gmail.com Subject: SVP Bharuch Venue: SDP HR SOLUTION 611 Golden Square Bs Dmart Bholav Bharuch Required Candidate profile Autoclave Operator Granulation Operator Manufacturing Operator Grinding Operator Washing Tunnel Operator Ampoule Filling Operator Vial Filling & Sealing Operator Lyo Operator Labelling Operator

Responsibilities: Supervise daily manufacturing operations for sterile injectable products (vials, ampoules, lyophilized, or PFS). Ensure compliance with cGMP , GDP , and regulatory standards (USFDA, WHO, MHRA). Oversee aseptic operations like compounding, filtration, aseptic filling , and lyophilization . Lead and train production staff in cleanroom behavior and SOP adherence . Maintain accurate batch records , logbooks, and documentation. Handle deviations, CAPA, and support audits and regulatory inspections. Coordinate with QA, QC, and Engineering for smooth production flow. Ensure equipment readiness and proper cleaning/sterilization processes. Required Skills Experience with oncology in...

Dear Candidate, Greetings from Intas Pharmaceuticals Ltd.! Intas Pharmaceuticals is a leading, vertically integrated global pharmaceutical company headquartered in Ahmedabad, India, with a strong presence in over 85 countries. Driven by innovation and quality, Intas is committed to developing and manufacturing affordable medicines that improve lives across the world. We are pleased to announce a Walk-In Drive for our SEZ Plant for professionals experienced in Injectable/Parenteral Manufacturing operations including Sterile Aseptic Autoclave Clean Area Lyophilization processes Experience Required: - 3 to 12 Years Qualification Required: - Diploma / ITI Walk-In Drive Details: - Date: Sunday, 2...

Industry: Pharmaceutical / Biologics / Injectables Experience: 18+ years About the Role We are seeking a dynamic engineering leader to oversee strategic project execution, equipment reliability, and regulatory compliance across injectable and biologics manufacturing facilities. This role plays a pivotal part in ensuring seamless alignment between engineering and manufacturing operations while driving continuous improvement and audit readiness . Key Responsibilities Lead end-to-end project deliveries design, installation, commissioning & qualification Manage engineering operations, maintenance, and utilities (clean & black) Align Capex & Opex budgets with manufacturing goals Ensure compliance...

Candidate should be M.Pharmacy/Ph.D with 20 to 25 years of experience in Injectable development from a reputed pharma company for regulated markets like USA/Europe Develop injectable products from concept to market launch, ensuring compliance with regulatory requirements. Lead cross-functional teams to design, develop, test, and commercialize injectable products. Collaborate with stakeholders to identify project goals, timelines, and resource allocation. Ensure effective communication among team members, customers, and partners throughout the product lifecycle. Provide technical guidance on injectables development processes and procedures. Note: Candidates who are having relevant experience ...

Role & responsibilities : Production Planning: Manage daily manufacturing activities, manpower, and ensure timely, quality production as per schedule. Documentation & Compliance: Complete and review BMRs, follow SOPs, and ensure all work meets cGMP and regulatory standards. Coordination: Work with QA, QC, Stores, and Maintenance teams for smooth production and equipment upkeep. Team Management: Guide, train, and motivate team members to follow company policies and good manufacturing practices. Safety & EHS: Maintain a safe work environment, ensure PPE usage, report incidents, and follow all EHS rules. Process Improvement: Support productivity enhancement, cost-saving ideas, and new technolog...

As a Lyophilization Specialist at our stem cells manufacturing company in Hyderabad, your role will involve overseeing the freeze-drying process and ensuring optimal performance. You will be responsible for preparing and executing lyophilization cycles, monitoring equipment, maintaining documentation, troubleshooting issues, and collaborating with cross-functional teams to meet production goals and quality standards. Key Responsibilities: - Oversee the freeze-drying process and ensure optimal performance - Prepare and execute lyophilization cycles - Monitor equipment and maintain documentation - Troubleshoot issues related to lyophilization - Collaborate with cross-functional teams to meet p...

Role & responsibilities Manufacturing of Lyophilized Drug Product Aseptic Blending & Filling Injectable Filling Lyophilization BMR Preparation cGMP Practices, Media Preparation, Vial Washing and De-pyrogenation, Validation, Labeling & Packaging, Documentation Preferred candidate profile Aseptic handling Sound knowledge of QMS Sound knowledge of cGMP, GDP

Role & responsibilities Lead RT-PCR and molecular POC-based IVD product development under design control. Provide technical expertise in product design, experimental planning, execution, and data analysis. Ensure product robustness and performance through stability/analytical validation and clinical validation studies. Develop and implement QC procedures for critical reagents and processes. Lead development of Polymerase and Lyophilization for molecular diagnostic applications. Translate customer and market needs into product requirements and technical specifications. Define project plans, deliverables, milestones, and risk mitigation strategies across multiple product development programs. ...

Pfizer Healthcare India Private Limited - Visakhapatnam Hiring Diploma Pharmacy Freshers Job Role - Junior Associates - Manufacturing Eligibility Criteria: Diploma Pharmacy only (2025 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 t...

Company Description Stem cells manufacturing company focusing on a premium and equitable product. Role Description This is a full-time on-site role for a Lyophilization Specialist located in Hyderabad. The Lyophilization Specialist will be responsible for overseeing the freeze-drying process, monitoring equipment, and ensuring optimal performance. Additional responsibilities include preparing and executing lyophilization cycles, maintaining documentation, troubleshooting issues, and collaborating with cross-functional teams to meet production goals and quality standards. Qualifications Experience with lyophilization, freeze-drying processes, and understanding of thermal properties Knowledge ...

Candidate should be M.Pharmacy/Ph.D with 20 to 25 years of experience in Injectable development from a reputed pharma company for regulated markets like USA/Europe Develop injectable products from concept to market launch, ensuring compliance with regulatory requirements. Lead cross-functional teams to design, develop, test, and commercialize injectable products. Collaborate with stakeholders to identify project goals, timelines, and resource allocation. Ensure effective communication among team members, customers, and partners throughout the product lifecycle. Provide technical guidance on injectables development processes and procedures. Note: Candidates who are having relevant experience ...

Biological E. Limited (BE) invites experienced professionals to join its Specialty Injectables Business located in Genome Valley, Shamirpet, Hyderabad . Available Positions listed below: 1. PRODUCTION PHARMA (Injectables) • Designation: Officer / Senior Officer / Executive / Senior Executive • Qualification: Diploma / B.Sc / B.Pharm / M.Pharm / M.Sc • Experience: 2 to 10 years • Roles: Filling / Autoclave / Compounding / Lyophilization 2. QUALITY CONTROL (Injectables) • Designation: Executive / Senior Executive • Qualification: B.Pharm / M.Sc • Experience: 2 to 6 years (Injectables) • Roles: Raw Materials / Finished Goods / Stability 3. MICROBIOLOGY (Injectables) • Designation: Executive / S...

1. Production Operations Plan, execute, and monitor day-to-day injectable manufacturing operations (Liquid / Lyophilized / SVP / LVP). Ensure adherence to batch manufacturing records (BMR) and standard operating procedures (SOPs). Coordinate with Planning, QA, QC, Engineering, and Stores for smooth production activities. Monitor in-process checks and ensure timely completion of batches. Ensure line clearance before starting operations. 2. Compliance & Documentation Ensure compliance with cGMP, WHO, USFDA, EU, MHRA, and other regulatory standards. Review and approve BMR, BPR, and related production documentation. Participate in internal and external audits (regulatory and customer). Initiate ...

We are looking for a Mechanical Technician to join our Production Department at Lyophilization The ideal candidate should have hands-on experience in machine assembly, fabrication, and mechanical fitting within an engineering or manufacturing setup. Key Responsibilities: Assemble mechanical components and subassemblies for lyophilization systems. Work on fabrication, fitting, and alignment of mechanical parts as per engineering drawings. Support production and assembly line operations to ensure timely project delivery. Coordinate with design and quality teams to ensure adherence to technical standards. Perform testing, inspection, and troubleshooting during assembly and installation. Maintai...

We are hiring for Plant Maintenance/ Process Maintenance Engineer at Amneal Pharmaceuticals Ahmedabad. Only for Pharma experience candidates : Job description: We are looking for passionate and skilled professionals to join our Engineering Injectable plant maintenance Department. (Instrumentation / Electrical / Mechanical). Position: Officer / Executive Qualification: Diploma / B.Tech. (Instrumentation / Electrical / /Mechanical) Experience : 4 to 9 Years Location: Amneal, SEZ Matoda, Ahmedabad What We are Looking For : Hands-on experience in Preventive & Breakdown Maintenance of injectable manufacturing lines such as : Vial Line, Microfiber line, PFS Line & Ophthalmic Line. Schedule mainten...

Role & responsibilities Cell Culture & Production Support: Perform aseptic handling and maintenance of cell cultures (e.g., Vero, BHK or other cell lines) in adherent and/or suspension formats. Prepare and sterilize culture media, buffers, and reagents as per batch requirements and SOPs. Monitor and record cell growth parameters, viability, and morphology. Scale-up cell cultures for downstream processing or viral seed production. Facility & Environmental Monitoring: Conduct routine facility checks including temperature, humidity, pressure differentials, and cleanroom conditions. Coordinate and ensure compliance with environmental monitoring schedules (viable/non-viable particles, surface, an...

As a Deputy Manager/Manager Level1 (Production) at Polypeptide Group, you will be responsible for managing daily production operations, ensuring compliance with GMP standards, and coordinating with various teams to meet production targets. Your expertise in the Peptide Industry, particularly in solid phase peptide synthesis, purification, and lyophilization, will be essential for maintaining a high level of productivity and quality. Key Responsibilities: - Oversee daily production activities and planning to meet monthly, quarterly, and yearly targets. - Manage inventory to maintain optimal stock levels. - Prepare MBPRs, SOPs, and risk assessment documents. - Investigate deviations, identify ...

Opportunity to work with a global brand Opportunity to work in a high visibility senior leadership role About Our Client An international healthcare firm dedicated to delivering lifesaving medicines and technologies, with manufacturing sites and research centers located in several countries. Job Description Strategic Leadership: Manage all aspects of the sterile injectable plant's operations, including production, quality, engineering, supply chain, and EHS. Regulatory Compliance: Maintain full adherence to internal policies and external regulations. Operational Excellence: Promote continuous improvement in manufacturing efficiency, cost control, and product quality; lead digital initiatives...

For Production (Injectable): Exposure pertaining to Groninger vial filling, Groninger Bottle fiiling, Fedegari Autoclave, NKP vial Filling machine, lyophilizer, Spray dryer, Aseptic process, complex manufacturing, Exposure to CIP/ SIP, SKID manufacturing, pre-fill syringe, QMS is required For Production (OSD): Exposure of granulation, compression and coating process, BMR, Change control, CAPA, For Engineering: Exposure of maintenance of Sterile Manufacturing Plant, maintenance of Autoclave, Filling machine - Vial, Ampoule, Ophthalmic, Lyophilizer, Freeze dryer machine, BFS machine is required Job Location: Sun Pharmaceutical Medicare Limited (Baska) : Nr. Hotel Sarvottam, Survey NO 22 & 24 ,...

Role : Executive Small Volume Parenteral Manufacturing Location: Ahmedabad Department: Injectable / Sterile Production Key Responsibilities: Production Operations: Plan, organize, and execute the manufacturing batches of small volume injectable products. Operate / supervise key equipment: vial/ampoule washing, sterilization (autoclave, filtration), filling, sealing, capping, tunnel sterilizer, lyophilizer (if applicable) etc. Ensure line readiness, material dispensing, line clearance before/after operations. Aseptic Process & Sterility Assurance: Maintain cleanroom operations, gowning, environmental monitoring, microbial monitoring. Ensure correct operation of aseptic filling / sterile filtr...

Responsible for Total Vaccine manufacturing Process Required Candidate profile Graduate / post graduate in life science with 18+ yrs experience in viral vaccine manufacturing process Minimum 5 yrs experience in top management posiiton must.

Biological E. Limited invites experienced, dynamic and self-motivated candidates with 2 to 8 years of experience for the below positions at its Vaccine Business, Shamirpet, Hyderabad: Designation: Sr. Executive/Executive/Sr. Officer/Officer Qualification: M.Sc. (Lifesciences) / B. Pharmacy / Diploma / B.Sc. / ITI PRODUCTION BULK MANUFACTURING (DRUG SUBSTANCE / ANTIGENS) Desired Experience: Applicants with relevant experience in vaccine, biosimilars, or injectable manufacturing will be considered. Perform upstream and downstream activities for bacterial or viral antigens. Execution of production batches in both upstream and downstream areas. Focus on timely execution to ensure that the proces...