Company Jobs

Responsible for managing QMS activities including deviations, change control, CAPA, and OOS/OOT, ensuring timely closure and compliance with GMP and data integrity standards.

Must have knowledge of preparation and execution of SOP, manufacturing. Packing and qualification document of SCADA based equipment.

Ability to understand and analyses the complex data and performs the activities including accessing the case in Argus, code and enter data.

MPharm / BPharm / MSC/ BSC ; Experience in Visual inspection – Automatic inspection Machine, leak test machine.

Looking forward to onboard Injectable Production Supervisors who have experience in the Ophthalmic machine, PFS filling machine, aseptic batch manufacturing and aseptic area experience.

Should have experience in OSD process equipment maintenance. Knowledge on Granulation, compression, capsulation and coating process.

Calibration and qualification of analytical instrument, Handling of Working standard, column and training management.

Looking for a dedicated and experienced professional to join our Regulatory Affairs team.

Conduct packaging trials & support scale-up to commercial production. Perform compatibility & stability studies with QA / QC teams. CIRO Pharma