Hyderabad

The Clinical Research Lead will oversee and manage clinical research activities within the organization. This role involves designing, implementing, and monitoring clinical trials to ensure they meet regulatory requirements and organizational goals.

This is a non-supervisory position in Reference Standard Laboratory responsible for performing the required tests as part of the project and maintaining the GLP environment in the Laboratory. The incumbent will utilize his or her technical expertise, knowledge of pharmaceutical analysis in collaborative testing, efficient and effective laboratory operations.

R&D Data Steward plays a critical role in the intersection between business and data, where stewards will guide business teams on how to unlock value from data. This role will drive definition and documentation of R&D data standards in line with enterprise.

Collecting and submitting in-process samples, finished product samples, stability samples, control samples, cleaning samples, and other samples as per the respective procedures, batch manufacturing records and packing records, protocols. Conducting AQl inspections and periodic inspections of control samples

B.Pharmacy or Pharm.D. Age below 30 years. 2 years experience coordinating in clinical trials. Knowledge of MS Office suite; document scanning, uploading, email communication and database management.

Compression, Coating, Capsule Filling, FBP. QC Microbiology, IP/FP, Stability, GLP,RM. QA IPQA, AQA, APQR.

Familiarity with high-performance organizational tools and a strong understanding of digital manufacturing processes, computer system validation requirements, and quality management within biologics production and quality.

Provides inputs for selection of the equipment Estimates the batch size based on available equipment at the receiving site. Assists in evaluating the suitability of partners development, manufacturing facility for technology transfer.