Hyderabad

Formulation and process development activities for parenteral pharmaceutical products. Pre-formulation, compatibility, stability and optimization studies.

B. Pharm M. Pharm M.Sc. Chemistry. Chromatographic analysis (HPLC) with Empower 3 software & LI MS Awareness CMP documentation & data integrity, HPLC Testing of raw materials, in-process & finished products

Supervise and coordinate manufacturing operations in Oncology production areas. Manage Granulation, Compression, Coating, and Packing activities.

B.Pharma + M.Pharma , M.Sc. / Master’s degree in Pure or Applied Sciences, including Biochemistry, Biotechnology, Microbiology, Nursing, and other relevant Life Sciences disciplines, MBBS degree or a Doctorate in Pure or Applied Sciences.

Master degree in Science (Plant Pathology/ Entomology/ Nematology/ Agricultural Biotechnology/ Biotechnology/ Botany/ Zoology/ Molecular Biology/ Plant Genetic Resources/ Life Sciences from a recognized University. at ICAR-NBPGR Regional Station

Established in 2016, ANNORA Pharma is committed to provide medicines with highest quality, safety and efficacy that meets the needs of the customers with applicable statutory and regulatory requirements.

Supervision of dispensing, compounding and filtration activities; cGMP, SOP and BMR compliance; line clearance and in-process checks; batch documentation and reconciliation; coordination with IPQA, QC, Microbiology and Engineering; handling of deviations, change controls and investigations; audit and regulatory inspection readiness.

To coordinate and author documents needed for regulatory submissions, ensuring the coordination and integration of the scientific, medical, and regulatory input from cross-functional team members.

Postgraduate degree in a Life Sciences / Health Sciences / Public Health / Clinical Research with post-qualification experience OR PhD. clinical research/RCT coordination, GCP, data management, regulatory documentation and transplant/infectious-diseases research