Discover exciting career prospects with Dr Reddy’s in Visakhapatnam, where innovation meets growth. Apply now for the role!

About Dr Reddy’s Company:

Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.

We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.

For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets).

Hiring Roles in Dr Reddy’s Company:

1. Team Member – Quality Control (RMPM) – Click Here
2. Team Member Quality Control (Stability) – Click Here
3. Team member IPQA – Click Here

Hiring Locations of Dr Reddy’s Company:

1. Team Member – Quality Control (RMPM) – VISAKHAPATNAM
2. Team Member Quality Control (Stability) – VISAKHAPATNAM
3. Team member IPQA – Pydibimavaram

Education Qualification of Dr Reddy’s Company:

Qualification: B. Pharmacy / M Pharmacy/ MSc (any branch)

Experience for the Roles:

1. Team Member – Quality Control (RMPM) – 6 – 8 years
2. Team Member Quality Control (Stability) – 2 Years
3. Team member IPQA – 5 to 8 years

Job Description Quality Control (RMPM):

Job summary

We are seeking an individual to test samples and release results within Turnaround Time (TAT) for commercial RM/PM 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.

Job Description Quality Control (Stability):

Job summary

We are seeking an individual to test samples and complete within window period for 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.

Job Description for Team member IPQA:

Knowledge of Process validations and new product Introduction.

Experience in Nasal formulations.

PPQ Protocols, Reports review, Risk Assessments review approval.

Performing in-process activities such as line clearance, In-process checks, AQL checks, and collection of Samples (blend /Finished product/stability samples ).
Sampling .and reconciliation of packing material and finished goods products during packing operation.
Review of Batch Production/packing Records.
Investigate incidents, OOS, and OOT and ensure action plans.
To ensure cGMP (Current Good Manufacturing Practices) compliances on the shop floor.
Understand manufacturing and packing equipment and its function.
Review Equipment’s Alarm, Event, and Audit trail

How To Apply:

Interested candidates can apply above the links we encourage you to visit their website at click here to learn more about their work and the exciting projects

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