Analyst/Chemist-Quality Control tests samples, reagents from all phases of the manufacturing process to ensure the product quality meets the standards. The individual is responsible for the testing of in-process/input raw materials, packaging materials, product stability of samples, in-process intermediate samples, finished products, preliminary investigation in case of out of specification results, laboratory incidents and handling/preparation of standards. The person is responsible for preparing the documents for reporting the test results and ensures compliance with cGMP, GLP and workplace safety while handling hazardous materials. The role holder also carries out testing of process validation samples and cleaning validation samples.

A Assistant- Maintenance (Pharma, Biologics and Medical Device Facility) assists maintenance technician and supervisor in carrying out maintenance activities and performing basic machining, fitting and assembling activities of machinery and utilities like Heating, Ventilation, and Air Conditioning (HVAC), Water, Gases, Steam, and Electricity. The individual is responsible for carrying out reporting and documentation for maintenance activities as per Good Manufacturing Practices (GMP). The job holder is also responsible for maintaining a healthy, hygienic, safe and secure working environment.

The Assistant- Manufacturing and Packaging (Pharma, Biologics and Medical device) supports in manufacturing and packaging activities by performing a combination of tasks. The job role holder also supports the team in maintaining a healthy, safe and secure working environment.

The Assistant- Secondary & Tertiary Packaging (Pharma, Biologics and Medical device) supports the packaging team in secondary and tertiary packaging activities by performing a combination of tasks. The job role holder also supports the team in maintaining a healthy, safe and secure environment and disposal of waste packing material as per regulatory guidelines.

Associate-Clinical Research Management (Pharma, Biologics and Medical devices Facility) supports clinical trial activities, carries out reporting and documentation for monitoring of research activities to ensure regulatory compliance and Good Clinical Practices (GLP) as per ICH and coordinates with site staff members, investigators, SMO and Sponsor

Associate-Clinical Research Management (Pharma, Biologics and Medical devices Facility) supports clinical trial activities, carries out reporting and documentation for monitoring of research activities to ensure regulatory compliance and Good Clinical Practices (GLP) as per ICH and coordinates with site staff members, investigators, SMO and Sponsor

Associate- Regulatory Affairs and Intellectual Property prepares dossiers to support appropriate licensing, marketing and legal compliance of products and ensure products comply with current regulations. The job role holder carries out proper documentation and reporting for dossier preparation and assist in intellectual property management.

Associate- Regulatory Affairs and Intellectual Property prepares dossiers to support appropriate licensing, marketing and legal compliance of products and ensure products comply with current regulations. The job role holder carries out proper documentation and reporting for dossier preparation and assist in intellectual property management.

Associate- Regulatory Affairs and Intellectual Property (IVD and Medical Devices) prepares dossiers to support appropriate licensing, marketing and legal compliance of products and ensure products comply with current regulations. The job role holder carries out proper documentation and reporting for dossier preparation and assist in intellectual property management.

Associate- Regulatory Affairs and Intellectual Property (IVD and Medical Devices) prepares dossiers to support appropriate licensing, marketing and legal compliance of products and ensure products comply with current regulations. The job role holder carries out proper documentation and reporting for dossier preparation and assist in intellectual property management.

Associate- Store (Pharma/ Bio Pharma / Medical Devices) is responsible for inspecting the broad level physical characteristics of the material, placing them in correct storage area, reporting and documenting, housekeeping, disposing waste packaging material, and maintaining a safe working environment.

Bioinformatics Associate is also known as Bioinformatics Analyst or Computational Biologist. He/she creates mathematical models, develops dynamic simulations and performs pattern analysis of biological systems. The person is also responsible for the design of databases. He/she implements algorithms for data processing to identify and classify components of a biological system. The individual performs collection, storage and archival of primary data. He/she is expected to use machine learning for analysis of biological data, in consultation with Bioinformatics Scientist, researchers and other cross-functional stakeholders.