3-4

Responsible for process validation and cleaning validations and respective documentation. Responsible for Equipment and utilities qualification and periodic validation.

Experience in IPQA, QMS, validation, documentation, aerosol manufacturing, filling machine, sterile manufacturing.

Liaise with key partners, including Pfizer Country Organizations, Clinical Development, License Partners, and other stakeholders regarding safety data collection and data reconciliation.

M.Pharm/B.Pharm/M.Sc/B.Sc; IPQA/APQR/Validation and Qualification; Handling Change Control/ CAPA/ Deviation/ Investigation and Audit Management; Issuance and Retrieval of GMP Document

Ipca is a fully integrated, rapidly growing Indian pharmaceutical company with a strong thrust on export. Ipca'a API and Formulation produced at world class manufacturing facilities are approved by leading drug regulatory authorised including the USFDA.

To provide scientific support to analysts at bench level for developing & qualifying methods required for product Analytics. Execution of critical experiments for specific deliverables.

Hetero Drugs is an Indian pharmaceutical company and the worlds largest producer of anti-retroviral drugs. Hetero business includes APIs, generics, biosimilars, custom pharmaceutical services, and branded generics.

The ideal candidate will ensure smooth running of multiple cell-based and biochemical assays while maintaining highest quality and integrity of data and meeting established timelines.

You will be responsible for generating new product ideas from Key Opinion Leaders interactions, prioritizing these ideas, preparing business cases, analyzing market and competitor data, and handling creative aspects like branding. The aim is to ensure the timely launch of products that address unmet market needs.