Team Member Qc

1 week ago

Hyderabad Telangana, 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 conducting testing of in-process, finished product and stability. The role involves ensuring accuracy in documentation, adherence to safety procedures, reporting discrepancies, and maintaining lab safety.

**Roles & Responsibilities**
- You will be responsible for conducting sampling and analysis of packaging and raw material samples as allotted by the group leader.
- You will be able to handle HPLC, GC, Dissolution apparatus, LIMS software and Empower.
- Should have knowledge on CGMP, GLP, 21 CFR and any other regulatory requirements.
- 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 Analysis), and using proper PPE (Personal Protection Equipment) at the workplace are emphasized.
- You will oversee the handling and upkeep of the chemical and solvent store, preparation of Spec-check, catalog, and result entries, as well as maintaining volumetric solutions and reagents.
- Your role also includes preparation of out lab testing samples (as required), timely destruction of samples as per SOP, printing COA (Certificate of Analysis), completing assigned training, and any additional responsibilities assigned by the Group Leader.

**Qualifications**
**Educational qualification**:A Bachelor’s/master 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**
- Proficient in various analytical techniques, including sampling and analysis of packaging and raw material samples.
- 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 a

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