After a journey of growth spanning 27 years as Cadila Healthcare Ltd. and the Zydus Group, we have evolved and transformed ourselves in response to the changing times. Our legacy of over 70 years in healthcare and being dedicated to life in all its dimensions is reaffirmed in our new mission, vision and purpose. Unifying ourselves under the Zydus name, Cadila Healthcare Ltd., is renamed as Zydus Lifesciences Ltd.
Executive / Sr. Executive in Viral vaccine department
M.Sc. in Biotechnology / Microbiology with 4-8 years of experience in viral vaccine department. Candidates would be responsible for propagation and maintenance of MRC-5 cells / vero cells in TCF's, cell stacks and roller bottles, aseptic operation,preparation of master and working banks of cell lines and viruses, virus culture and harvesting in systems like flask, cell stacks and roller bottles,preparation of media, buffers, stabilizers and sterile filtration, SOP's, BMR's, protocols and documents related to the process. They should have knowledge on GMP, qualification of instruments / equipment and biosafety.
Executive / Sr. Executive in R&D - Process Development department
M.Sc. in Biotechnology / Microbiology with 4-8 years of experience in R&D -Process Development department.The job requires planning, execute / supervise and evaluate bacterial fermentation experiments independently and systematically developing / improving, bacterial fermentation processes and primary recovery on the basis of vaccine upstream processing (U5P), developing strategies to scale-up / down and process control and training the trainees / scientists on process development / troubleshooting efforts. Should have experience in technology transfer from small scale to large / production scale, in scientific and technical documentation supporting developmental activities and maintaining of inventory required for the activities.
Executive / Sr. Executive in IPOA department
M.Sc. in Biotechnology / Microbiology with 4-8 years of experience in IPQA department. Candidates would be responsible for quality oversight of personnel, process and practice to meet the cGMP and compliance requirement, for providing line / equipment clearance prior to dispensing, manufacturing and packaging and validation activities during batch and product change at DS & DP manufacturing facilities. Should also ensure shop floor compliance, for ensuring sampling as per defined frequency and methodology during batch manufacturing of all validation activities and exhibit batch manufacturing and do the entry of the samples in LIM5 software, reviewing executed batch manufacturing and batch packing record for accuracy, completeness and compliance.
The role also requires reviewing of manufacturing log books (for e.g.. area cleaning logbook, equipment usage logbook) and environmental monitoring records (for e.g.. temperature and humidity logbook) and ensuring contemptuous documentation, for preparing SOPs related to QA-operation. for collecting, compiling and taking follow ups from cross functional departments for APQR data compilation & APQR preparation. Should also participate in investigation of reported microbial data deviation at DS & DP Manufacturing facility, participate in execution of process validation activities, change campaign cleaning validation and inactivation kinetics study etc, review electronic records like PLC, SCADA. equipment printouts, audit trails, alarms and events as per site SOPs.
Senior Executive to Deputy Manager in Vaccines QC
MVSC with 6-12 years of experience in vaccines QC related to bacterial, recombinant and viral vaccine products. The role requires designing in-vivo and in-vitro experimentation for vaccines at various stages of development, help in designing non-clinical safety studies in animal models, maintenance of lab animals and animal house facilities according to regulatory guidelines, execution of the study according to the study design.
The role also requires maintaining the animal husbandry record of the animal house, preparing analytical method development protocol & report (animal experiments) for technology transfer and reviewing of PCT protocols and reports, procuring of animals from vendors, animal receiving, quarantine and grouping and monitoring animal’s health, dose optimization study in mice.potency study: in-vivo potency study in mice for stability and GMP(regulatory) batches of R&D and QC-R&D & animal house Moraiya and ZRC. The role also requires hyper immune sera generation in rabbits. Should also conduct immunogenicity studies in rats and rabbits in the support for PCT study and support in in-vitro assay (Antibody analysis of serum samples).
Job Location : Vaccine Technology Centre, Ahmedabad
Candidates having exposure to regulatory requirements is essential alongwith a background in the vaccine industry. Interested candidates can share their CVs with email@example.com
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