New

Senior Executive-Operator

Hyderabad - R&D

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company’s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com.

Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.

About the Role

  • OSD Operator plays a critical support role in Oral Solid Dosage (OSD) formulation development, working closely with formulation scientists to execute laboratory‑scale manufacturing activities in a safe, compliant, and well‑documented manner. The role focuses on operating and maintaining OSD equipment, supporting formulation trials, and ensuring strict adherence to GLP, SOPs, data integrity, and EHS requirements

Key Responsibilities

OSD Operations & Equipment Handling

  • Operate and support laboratory‑scale OSD equipment including dispensing, granulation, FBP, HME, blending, compression, and coating as per approved SOPs and protocols.
  • Set up, monitor, and clean OSD equipment such as blenders, granulators, compression machines, coating pans, and associated accessories under supervision.
  • Support formulation trials, optimization studies, and batch execution activities
  • Calibration, Maintenance & Equipment Compliance
  • Perform daily calibration / verification of balances and pH meters and ensure proper documentation in logbooks
  • Ensure timely annual calibration and preventive maintenance of formulation equipment in coordination with Instrumentation / Engineering teams
  • Identify, label, isolate, and report equipment malfunctions, deviations, or abnormal performance immediately.
  • Comply with EHS requirements, PPE usage, and safe material handling practices.
  • Support handling of raw materials during batch operations and disposal of expired or discarded chemicals as per SOP.
  • Report safety observations, incidents, or near misses immediately.
  • Ensure Cleanliness, Hygiene, OSD and injectable lab as per the cGMP practices.
  • Daily Temperature & Humidity monitoring in Lab Refrigerator & Freezer and retrieving the Data Backup in frequent intervals.
  • Preparation of RGP & NRGP in coordinating with technical team and providing numbering for the Same and maintaining a Track.
  • Ensure the receipt of the material at respective CRO & CMO.
  • Follow up for the materials which were sent out through RGP.
  • Maintenance of minimum spares related consumable items in co-ordination with the Warehouse team.
  • Maintaining adequate facilities in the site for Collection, Storage and Disposal of Hazardous & Non-Hazardous Waste from the Site to authorized third parties in co-ordination with the EHS department.
  • Shall Fulfill and support all the EHS requirements at the site.

Required Skills and Experience

  • 8+ years of experience as a Working Professional in similar field.

Preferred Qualifications

  • Shall hold any bachelor’s degree relating to science or equivalent.

 

By applying for this role, you confirm that you are mentally and physically capable of fulfilling the job responsibilities detailed in the job description without any restrictions. If you have any concerns or even the slightest disability that may affect your ability to perform the job, please inform HR in advance.

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