Team Member Qc

7 months 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.
- To follow Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- To follow Laboratory Safety Standards and Practices.
- Responsible for the execution of IP/ FP /Stability samples analysis.
- Responsible issuance of new STPs/Specifications from QA and submission of obsolete STPs/Specifications to QA.
- Responsible to report/highlight discrepancies in Procedures / Products / People practices/ Materials/ Systemic issues to the Group Leader and Functional Head in time.
- Responsible for perform the analysis as per the respective SOP or STP or GTP.
- Responsible for do the documentation online and error free.
- Responsible to ensure Calibrated Instruments / Equipment are used for analysis.
- Responsible for maintenance & issuance of Working / Reference / Impurity Standards Used for analysis.
- Responsible to operate the Instruments / Equipment with utmost care and as Instructed in the relevant SOP.
- To report Incidents / OOS / OOT and unexpected results in time to the Group Leader.
- Responsible for management of chemicals, solvents, Reagents, standards& miscellaneous Materials from Engineering store.
- Responsible for adherence to the Stability Management procedure.
- Responsible for ensuring the disposal of IP/FP/Stability samples after the Completion of analysis.
- Responsible for support to perform all the LST related activities.
- Responsible for maintenance & issuance of Columns for chromatography used for Analysis.
- Responsible for comply any other responsibilities given by the Supervisor.
- Responsible for support during Breakdown Maintenance and Preventive Maintenance of Instruments/ Equipment.
- Responsible for proper maintenance of Documents, Register & Booklet and reconciliation As applicable.

Responsible for analytical method validation and analytical method transfer activities
**Qualifications**
**Educational qualification**:A Bachelor’s degree in Chemistry, Analytical Chemistry, or a related field

**Minimum work experience**: 2 to 5 years of experience in a laboratory setting, preferably in the pharmaceutical or related industry

**Skills & attributes**:
***
**Technical Skills**
- Should able to handle the EMPOWER ,LIMS,LCMS and Chromatography analysis
- Experience with the operation and maintenance of analytical instruments, ensuring proper use and care as per SOPs.
- Competent in SAP activities related to sample tracking, documentation, and data entry.
- Knowledgeable about cGMP, SOPs, and STPs, ensuring accurate documentation and adherence to specifications.
- Adheres to safety precautions and procedures during analysis, emphasizing the importance of lab safety, JSA (Job Safety Analysis), and proper use of PPE (Personal Protective Equipment).
- Expertise in handling and upkeep of the chemical and solvent store, including the preparation and maintenance of volumetric solutions and reagents.

**Behavioural Skills**
- Keen attention to detail in analysis and documentation, ensuring accuracy in all tasks.
- Effective communication and collab

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