Company Jobs

Support execution of core data management activities across the study lifecycle, including database build, edit check testing, lab and coding setup, data cleaning, query management, reconciliation, and lock preparation.

Serves as medical writing lead for identified projects/programs and proactively plan and identify document preparation strategies.

Plan, track, and deliver submissions aligned with timelines and regulatory requirements. Manage risks, dependencies, and complexities in global regulatory environments.

Candidates possessing hands on experience in semi solid dosage forms may apply. Candidate should be willing to work in shifts.

Preparation of technical documents like development reports, batch manufacturing record and technology transfer documents.

Define and lead medicinal chemistry strategies for the design, synthesis, and optimization of novel drug, meeting project goals for potency, selectivity, ADME, and safety

Coating, Compression, Granulation, Packing, Ointment-External Preparation, lnjectable (Aseptic, Batch Manufacturing, Bulk Manufacturing, Dry Powder), Oral Liquid

Review, verify, and approve analytical data and chromatograms generated via HPLC and other lab instrumentation.

Resource Optimization: Maximize the utilization of high-speed manufacturing machinery (RMGs, FBDs, compression machines, auto-coaters, and capsule fillers) while minimizing downtime and changeover times between product campaigns. Bal Pharma