Senior Assistant, Granulation
Description: This role is responsible for performing a variety of tasks related to the processing and assembly of ingredients and pharmaceutical products within a regulated manufacturing environment.
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Officer, Quality Control
Description: This role is responsible for conducting in-process and final product quality analyses and inspections within a quality control laboratory in strict compliance with established standards a
Officer, Manufacturing Documentation
To follow the safety rules in the premises according to the company norms. •To handle Quality Management Documents like Change Control, Deviation etc •To prepare Failure Investigation Reports against
Officer, Autoclave
Description: •To follow the safety rules in the premises according to the company norms. •To maintain online the BMRs and other log books in the respective area as per cGMP and SOP. •Responsible for m
Deputy Manager, Process Engineering
Description: The role is responsible for leading, governing, and optimizing pharmaceutical manufacturing processes across production operations. The role ensures process design integrity, validation c
Senior Officer, Quality Control Testing
Description: This role is responsible for conducting in-process and final product quality testing and analyses in strict compliance with established standards and regulatory requirements within a glob
Officer, Quality Control Testing
Description: This role is responsible for conducting in-process and final product quality testing and analyses in strict compliance with established standards and regulatory requirements within a glob
Manager, IT User Support
Description: The role is responsible for delivering responsive, day-to-day IT technical support to employees across the organization, ensuring stable and secure operation of hardware and software syst
Officer, Quality Control
Description: Sampling and analysis of water (Chemical and Microbiological testing) and record relevant data. Microbiological environmental monitoring/compressed air monitoring of the clean area. Micro
Executive, Inhalation CMC
Description: This role supports the development of drug substances and drug products by contributing to the design and execution of analytical methods used to evaluate quality attributes across variou
Senior Executive, Validation Engineering, Technical Writing
To prepare validation documents such as Installation qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) and other Qualification documents for equipment /utilities/fac
Officer, Raw Materials
Required Experience of: Receipt, storage and dispensing of Raw Material & Packaging Materials as per their respective Sops. Online documentation for all transactions of materials and all activities wh
Officer, Quality Control
Description: To ensure compliance with cGLP regulations by analysis and calibration of all aspects of Quality Control at the manufacturing site To work as key core team member for LIMS activities. Pre
Deputy Manager / Manager - Clinical Trials management
Job Description: Scientific review of Protocol and related documents i.e ICF, CRF, Plans, logs and forms, etc. as per regulatory requirements. Review of SIV presentations prepared by CRO and check for
Senior Executive, Regulatory Affairs
Good knowledge of ANDA submission activities and post-approval procedures and related ICH and USFDA guidelines. API DMF and DMF Change Notification review with respect to USFDA regulatory requirement.
Executive, Regulatory Affairs
Description: Good knowledge of ANDA submission activities and post-approval procedures and related ICH and USFDA guidelines. API DMF and DMF Change Notification review with respect to USFDA regulatory
Executive, Regulatory Affairs
Good knowledge of ANDA submission activities and post-approval procedures and related ICH and USFDA guidelines. Exposure of the Solid oral dosage form / Sterile dosage form / complex dosage form / top
Executive, Regulatory Affairs
Description: Good knowledge of ANDA submission activities and post-approval procedures and related ICH and USFDA guidelines. API DMF and DMF Change Notification review with respect to USFDA regulatory
Executive, Regulatory Affairs
Description: Good knowledge of ANDA submission activities and post-approval procedures and related ICH and USFDA guidelines. Exposure of the Sterile dosage form / complex injectable dosage form and br
Trainee Officer, Vial Washing
To follow safety rules in the premises according to the company norms. •Timely completion of SOPs Training and On the job trainings related to respective area. •Responsible for the operation and clean
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