Vizag

Strong background and knowledge in manufacturing, compliance, and technology investigations, processes, and systems. Ability to work both independently and collaboratively.

Analytical Method development, Working knowledge in HPLC/UHPLC/GC, Any experience in peptide analysis and characterization is preferred. 

Formulation Development and expertise in inhalation/injectable dosage. Process Optimization and scale up

Liaise and influence the cross functional team to drive the site investigations to meet the supply reliability. Demonstrate the agility and lead the site investigation team to achieve the key quality and supply metrics. Championing in effective implementation of global investigations requirements at site.

Formulation development in solid orals tablets, Capsules, Pellets, Soft gels. Should have experience in extended release, delayed release, multiparticulate.

Experience into Analytical Method Validation of Injectable. Tech Transfer and Scale Up Activities.

Hands-on experience in handling the complete life cycle from review, submission and queries to post approval of Topical, Dermatological Formulations. Adherence to high quality, and regulatory standards in dossiers.

Bachelors or Masters in Pharmacy. Must have exposure in handling of Process Area maintenance like Manufacturing Vassals, Filling machine, Autoclave, Isolators and Lyophilization.

Graduation mandatory. Science/Pharma Graduate preferred. Should have relevant Team Handling and Pharma experience