Team Member Qc Fto

2 weeks ago

Andhra Pradesh, India Dr Reddy's Laboratories Limited Full time

Company Description
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).

'The Next and the New' is how we aim to continue to be the partner of choice - purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose - helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency

Dr Reddy's maintains a work environment, free from discrimination and is an equal opportunity employer.

We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in.

We treasure every talent, and recognize merit and diversity in our organization.

Job Description Job Summary**We are seeking an associate for the Quality team responsible For performing of Stability sample analysis through Manual/SAP/LIMS, maintenance of Stability chambers in QC department. The role involves ensuring accuracy in documentation, adherence to safety procedures, reporting discrepancies, and maintaining lab safety.

Roles & Responsibilities

  • Ensuring good laboratory practices (GLP), good documentation practices (GDP) and good manufacturing practices (GMP).
  • To follow Laboratory safety standards and practices.
  • For performing of Stability sample analysis through Manual/SAP/LIMS.
  • For calibration and standardization of Analytical instruments.
  • To report/Highlight discrepancies in
- procedures / products / materials /People practices/ Systemic issues to the team leader and functional head on time.

  • To ensure that the analysis is conducted as per the respective SOPs STPs and GTPs.
  • For maintenance of Stability chambers in QC department.
  • For review and approval of the stability protocols.
  • For loading and withdrawal of stability samples as per schedule.
  • For destruction of leftover samples after analysis.
  • To ensure that the documentation done is online and error free.
  • To ensure that only calibrated instruments / equipments are used for analysis.
  • To ensure that only valid working / reference / impurity standards are used for analysis.
  • To ensure that the instruments/ equipments are used with utmost care and as instructed in the relevant SOP.
  • To report incidents/ OOS/ OOT on time to the team leader.
  • To ensure the instruments / equipments and work area should be clean.
  • Preparation and standardization of volumetric solutions.
  • For maintenance of registers, logbooks used for analysis.
  • Testing of analytical samples as per the schedule and submit the reports online to the concern.
  • Result posting and other SAP and LIMS related activities for sample analysis.
  • Implementation of CAPA and notifications closure on time.
  • For sending the samples to contract laboratory for testing.
  • To perform stability compilations.
  • For chromatographic data and processing in Empower.
To perform any other task assigned by the reporting authority

  • You will be responsible for SAP activities, ROA (Record of Analysis) preparation, and reviewing analytical records and raw data against Specification and STP (Standard Testing Protocol).
  • You will ensure accuracy of the documentation before submitting it for the Group Leader's review or uploading online.
  • You will also be responsible for the proper use and care of instruments or equipment as instructed in relevant SOPs (Standard Operating Procedure), including cleaning before and after analysis.
  • You will adhere to safety precautions and procedures during analysis.
  • Your responsibilities include placing SOP/STP/reference standards at their designated locations after analysis, and reporting discrepancies or incidents promptly to the Group Leader.
  • Lab safety, following JSA (Job Safety A

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