4-5

Contribute to the development and implementation of new safety-related systems, processes, and procedures within the process. Support a performance-driven culture.

Plan and coordinate with various departments like QA, QC and Production, to project the document requirements for appropriate submissions. Co-ordination with clients for the tracking and status update of project plans.

Candidates having hands-on experience in Analysis of Raw Material, Packaging Material, Finished Goods, Stability, Method Transfer and Laboratory Investigations. Should have sound knowledge of QMS like Deviations, Change Control, Vendor Management etc.

To author and gain approval of scientific and regulatory submission documents that comply with global regulatory standards. To maintain key business relationships with appropriate cross-functional product team members.

01 to 05 with relevant functional experience in injectable manufacturing, Aseptic area operations, Packing, Visual inspection, QMS activities

Quality Management System oversight and implementation, Validation processes for production systems, In-Process Quality Assurance for General Injectable and Oral Solid Dosage forms.

Stallion Laboratories incorporated in 1988 as an integrated private sector Pharmaceutical Formulation Manufacturer, has acquired an unmatched record of managing niche product in formulations with a WHO GMP approved production facility and GLP qualified stringent quality control.

Experienced in handling Primary and secondary packing activities like Blister Packing, Carton packing, Case packing and Serialization. Experienced in Tube filling, Jar filling, Bottle filling etc. in primary packing line machine. Career - Expo at Vizag Packing - OSD & Derma

Sciences or Pharmacy Graduates with o to 5 years Experiences in parenteral manufacturing vial, ampoules, bottles of glass or Plastic through, BFS technology, Bag Line.