Company Jobs

Experience in solid oral dosage & liquid orals form in formulation & development department for regulated market

Handling QMS as per Regulatory requirements. Handling Deviations, CAPA, Change Controls, OOS investigations. Responsible to process internal quality audits.

Candidate should have good experience in execution and review of qualification activities, environmental monitoring, clean room validation, and cross-functional coordination with Engineering, QA, and Production teams.

Workmen allocation and manpower management on shift basis. Supervision of secondary packing operations, especially bottle lines. Compliance with cGMP, safety, and hygiene requirements.

Exposure to OSD Manufacturing operations like Granulation, Pellet coating, Compression, Coating, Capsules, Primary Packing

Seeking a highly experienced Regulatory Affairs professional to manage regulatory activities for parenteral (injectable) products across the LATAM region. The role involves end-to-end regulatory lifecycle management, ensuring timely submissions, approvals, and compliance with regional regulatory requirements.

The ideal candidate must have hands-on experience in ophthalmic formulations, along with strong expertise in autoclave handling and batch manufacturing processes. Knowledge of GMP and quality compliance is essential.

Masters Degree in Pharmacy or Life Sciences; MBA preferred. Strong understanding of Preclinical Testing Services and business development processes.