Associate, Manufacturing Injectables - Ahmedabad City, Gujarat, India

Description · Key Responsibilities Strategic Leadership & Technical Oversight · Drive the MSTG strategy for injectable manufacturing, aligning with corporate goals and regulatory expectations. · Lead cross-functional teams in the design, development, and optimization of manufactu ...

Description · Experience: · Minimum 2years of experience in a pharmaceutical production environment, with running of machine experience. · Hands-on experience with Batch Manufacturing, Ophthalmic machine and PFS machine. · Experience in Greenfield Projects, involving new facility ...

Description · Experience: · Minimum 2years of experience in a pharmaceutical production environment, with running of machine experience. · Hands-on experience with Batch Manfuacturing, Ophthalmic machine and PFS machine. · Experience in Greenfield Projects, involving new facility ...

Description · Greenfield Project Execution: · Assist in installation, commissioning, and qualification (IQ/OQ/PQ) of Optima PFS filling line, isolators, and associated equipment. · Participate in CSPE (Comprehensive Scientific Process Engineering) activities to ensure smooth and ...

Description · 1. To plan line wise activity as per production schedule  · 2. To follow SOPs and minimize the deviations  · 3.To work with GMP and compliance in manufacturing process.  · 4.To maintain cleanroom with defined cleaning frequency  · 5.To report if any abnormality / de ...

Description · Key Responsibilities Strategic Leadership & Technical Oversight · Drive the MSTG strategy for injectable manufacturing, aligning with corporate goals and regulatory expectations. · Lead cross-functional teams in the design, development, and optimization of manufactu ...

Description · Key Responsibilities:  · Responsible for preparation & review of the master documents of sterile manufacturing for parenteral facility.  · Responsible for preparation and review of protocols and reports based on the requirements. · Responsible for document managemen ...

DescriptionResponsible for preparation & review of the master documents of sterile manufacturing for parenteral facility.  · Responsible for preparation and review of protocols and reports based on the requirements. · Responsible for document management and preparation like BMR's ...

Description Responsible for document management like BMR's, BPR's, master SOP's etc. · Responsible for preparation & review of the master documents of production. · Responsible to ensure UAF working in area. · Responsible for the handling of change control, deviations, investigat ...

Description · Key Responsibilities: · Responsible for document management like BMR's, BPR's, master SOP's etc. · Responsible for preparation & review of the master documents of production. · Responsible to ensure UAF working in area. · Responsible for the handling of change contr ...

Description · To perform CCIT test of post media fill units.  · To perform observation of microbial plates exposed in manufacturing area.  · To perform media fill unit observation as per SOP.  · Responsible for reporting any OOS, Deviation to In-charge.  · Responsible for prepara ...

Description · Skills : · Continuous improvement & lean methodology · Lean Six Sigma Green Belt/ Black Belt methodology · Good communications skills with the cluster head · Data analytics · Manufacturing and Operational efficiency improvement skills · Key Responsibilities:  · Lead ...

Description · Key Responsibilities:  · Responsible to attend the training as per schedule and to ensure the training and work as per TNI. · Responsible to perform and monitoring all the activities related to Aseptic area. · Responsible to follow the preventive maintenance schedul ...

Description · Description: · To ensure compliance with cGMP and regulatory requirements by performing in-process quality assurance activities on the manufacturing and packaging shop floor, including real-time monitoring, documentation review, sampling, and area/machine clearances ...

Description · Key Responsibilities:  · Responsible for review of URS, DQ and vendor/ supplier's documents related to qualification. · Responsible for preparation and review of Validation/ Qualification protocol and report. · Responsible for execution and review of Qualification / ...

Description · 1. Strategic Leadership & Business Planning · Develop and implement the long-term strategy for CMO operations in alignment with business objectives. · Identify, evaluate, and onboard CMOs based on technical capability, capacity, compliance history, and cost competit ...

Description · Automation Strategy & Architecture · Define and implement standardized automation architecture across the facility, including PLC platforms, I/O configurations, communication protocols (e.g., OPC UA, Modbus, Ethernet/IP), and software frameworks. · Lead the integrat ...

Description · Automation Strategy & Architecture · Define and implement standardized automation architecture across the facility, including PLC platforms, I/O configurations, communication protocols (e.g., OPC UA, Modbus, Ethernet/IP), and software frameworks. · Lead the integrat ...