Dr.Reddys Laboratories Ltd Hiring for Team Member – Manufacturing/Team Member – QCl (Microbiology)

Dr.Reddys Laboratories Ltd Walk-in Interview.Dr.Reddys Laboratories Ltd Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue.

Important Details :

• Selection Process: The selection will be on the basis of Interview.
• Mode of Interview: Face to face
• Interview Rounds of Interview: HR
• Job Location: Pydibimavaram/Baddi

Vacancy details:

• Department: Team Member – Manufacturing/Team Member – Quality Control (Microbiology)
• Qualification: An M.Sc., M.Tech. or B.Tech. in Microbiology, Biochemistry, or Biotechnology/Diploma/ B.Sc./M.Sc.
• Experience:  2 years

Job Description : Greeting from Dr.Reddys Laboratories Ltd..!!!!

Job Summary

We are seeking an individual to test samples and release results within Turnaround Time (TAT) for commercial and stability batches, adhering to GMP (Good Manufacturing Practices). This role involves calibrating and maintaining assigned equipment within departmental and organizational guidelines, processes, and procedures. The primary objective is to ensure accuracy in results provided within timelines.

Roles & Responsibilities

• Your responsibilities encompass testing assigned samples and releasing data within defined timelines, ensuring absence of executional errors against established procedures. You will be responsible for preparing required reagents and buffers in alignment with the testing plan and ensuring the availability of equipment for analysis. 

• Your role involves documenting activities contemporaneously, adhering to Good Documentation Practices and compliance expectations, and conducting self-checks post-analysis to ensure accuracy.

• You will promptly inform the supervisor about risk actions, providing necessary data and analysis to support the investigation process. You will adhere to QMS (Quality Management systems) and closure timelines, actively participate in laboratory investigations and discrepancy closures, fulfilling defined roles in audits.

• Your responsibilities also include ensuring lab cleanliness, proper sample storage, chemical labeling, removal of expired material, usage of calibrated equipment, equipment calibration, maintenance, and qualification.

• You will address instrument-related issues and conduct root cause analyses (RCAs) for unknown problems, and play a crucial role in training new team members on analytical techniques.

Team Member – Manufacturing

You will be responsible for overseeing execution of day-to-day production activities.

• You will be responsible for guiding and coaching employees, monitoring their productivity, and overseeing regular equipment safety and maintenance.

• You will be responsible for performing batch execution in OSD (Oral Solid Dosage) manufacturing

• You will be responsible for execution and review of Documentations, eBMR (Batch Manufacturing Records),

• You will be responsible for ensuring product quality by maintaining cGMP (current Good Manufacturing Practices).

• You will be responsible for handling Compression  activities.

• You will be responsible for in process checks in compression and execute end to end activity in compression.

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