8 Filling Line Jobs

Experience in Vaccine/Injectable/Sterile manufacturing setup Review and evaluate facility, utility, process equipment & instrument design Prepare and review URS, DQ, FAT, SAT, IQ, OQ, PQ documents Conduct Computer System Validation (CSV) as per GAMP & 21 CFR Part 11 Coordinate with project teams to meet timelines and milestones Ensure compliance with GMP and regulatory standards Investigate deviations, failures, and non-conformances Identify root causes and implement CAPA Support audits and inspection readiness activities Job Location: Kadi, Gujarat ( Bus facility available for daily commute) Note: Immediate joiners will be preferred first

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

Experience in Vaccine/Injectable/Sterile manufacturing setup Review and evaluate facility, utility, process equipment & instrument design Prepare and review URS, DQ, FAT, SAT, IQ, OQ, PQ documents Conduct Computer System Validation (CSV) as per GAMP & 21 CFR Part 11 Coordinate with project teams to meet timelines and milestones Ensure compliance with GMP and regulatory standards Investigate deviations, failures, and non-conformances Identify root causes and implement CAPA Support audits and inspection readiness activities Job Location: Kadi, Gujarat ( Bus facility available for daily commute) Note: Immediate joiners will be preferred first

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

Experience in Vaccine/Injectable/Sterile manufacturing setup Review and evaluate facility, utility, process equipment & instrument design Prepare and review URS, DQ, FAT, SAT, IQ, OQ, PQ documents Conduct Computer System Validation (CSV) as per GAMP & 21 CFR Part 11 Coordinate with project teams to meet timelines and milestones Ensure compliance with GMP and regulatory standards Investigate deviations, failures, and non-conformances Identify root causes and implement CAPA Support audits and inspection readiness activities Job Location: Kadi, Gujarat ( Bus facility available for daily commute) Note: Immediate joiners will be preferred first

The Associate Engineer is responsible for completing basic level engineering assignments related to manufacturing or packaging operations. Assists in the development of standards and procedures. Assignments have clear and specific objectives requiring investigation of a limited number of variables. Contributes to design of pharmaceutical manufacturing systems, processes, facilities, and machinery. Applies and interprets standard engineering theory, concepts, and techniques. Complies with pharmaceutical industry standards and regulations. Performing and documenting the preventive maintenance and breakdown maintenance of all production equipment listed below: - Fluid bed equipment-combo (ACG a...

As a Technical Support Manager specializing in Filling and Capping for Rigid Packaging Division, located in Vashi, Navi Mumbai, you will be responsible for supporting both Indian and worldwide SACMI customers in establishing SACMI design on filling lines. You should have a minimum of 8 years of experience in this field. Your primary areas of responsibility will include troubleshooting filling line and capping issues, actively enhancing closures and preforms performance, providing training on capping and filling line aspects internally and to customers, as well as assisting customers with GMP for closure and preform production and related troubleshooting. You will collaborate with the service...

Role & responsibilities Job Description: We are seeking an experienced and proactive Project & Maintenance Engineer to support equipment installation, commissioning, and qualification activities in a regulated pharmaceutical environment. The ideal candidate will have 46 years of hands-on experience in executing engineering projects, maintaining production equipment, troubleshooting issues, and ensuring compliance with documentation and regulatory standards. Key Responsibilities: Execute engineering projects involving installation and commissioning of pharmaceutical manufacturing equipment. Participate in qualification activities including IQ/OQ/PQ for plant equipment as per GMP requirements....