Dr. Reddys Lab

Experience in testing of finished products, LST and stability samples. Preferably worked in FDA Approved organizations. Hands on knowledge of cGMP, GLP, 21 CFR and any other regulatory requirements.

A Masters M.Pharm or M.Sc. or M.Tech. or M.E. or Bachelors B.Tech or B.E. or B.Pharm. An understanding of the Process Development and Industrial perspective of Biotherapeutics/ Biosimilars. Basic understanding of analytical techniques, statistical analysis, data management and analysis.

Responsible to Injectable line clearance, material verification ,start-up checks and in-process checks as per the batch manufacturing record, and Batch Packing record.

Experience in reviewing specifications and STPs, ensuring data integrity, proposing QbD Quality by Design process changes, and participating in phase gate reviews

Graduate - Science or General B.Pharma, D.Pharma, MBA. Minimum 6 months experience in sales. Dr. Reddys Laboratories is an Indian multinational pharmaceutical company located in Hyderabad, Telangana, India.

Subject Matter Expert for Drug-Device Combination Products will serve as a key resource within the organization for technical expertise and regulatory guidance related to the development, manufacturing, and commercialization of drug-device combination products.

Drafting procedural documents including Standard Operating Procedures, Work Instructions and Guidance Documents to capture PV processes.

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

Pharma sales job; dynamic and experienced Key Account Manager to identify key stakeholders and concerned parties that are integral to the success of the sales and account management strategy, to maintain long-term cordial relationships with key customers.