Ciron has carved a niche for itself in the sphere of operations of manufacturing Ampoules, Vials, Eye / Ear / Nasal drops, Lyophilized products and Lyophilized bulk
Redacts patient identifying information, images in accordance with data protection guidelines, ICH GCP and GVP. Enters data into the safety database in accordance with Sponsor, customer specific guidelines and Company standards. Ensures current conventions are followed when entering cases into the Safety database.
M.Pharm/ B.Pharm/ MSc; 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.
M.Pharmacy; Responsible for Formulation Development of Nasal Formulations. Responsible for conducting Formulation Development Trials and documenting the details in LNB.
RA publishing will participate in the publishing of different regulatory activities. The focus will be to ensure 100% quality and timeline of the submission. This role will be the primary interface with the Regulatory Affairs Associate
Supervise production team operations. Handle equipment: Sifter, FBD, Dryer, Centrifuge, ANF, Spray Dryer, Reactor, etc.
Ensure compliance with GMP processes. Maintain BMR, BPR, and logbooks.
Candidates must knowledge on all areas of production activities. Like handling of GLR, SSR, Centrifuge, Driers, Blender, Shifter, Miler, Documentation review, and regulatory knowledge.