Quality Control Analyst

Posted 11 Hours Ago
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Baddi, Solan, Himachal Pradesh
Entry level
Pharmaceutical
We accelerate access to affordable and innovative medicines because Good Health Can’t Wait.
The Role
The Quality Control Analyst will analyze samples, conduct authorized transactions, adhere to safety practices and SOPs, and ensure compliance with GLP standards. Responsibilities include maintaining 5S practices, reporting incidents, verifying analytical results, and managing sample workflows under the supervision of the group leader.
Summary Generated by Built In

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 analyst for the Quality Control team who will be responsible for analysing assigned samples and conducting authorized transactions. The role involves following SOPs (Standard Operating Procedures), STPs (Standard Testing Protocols), GLP (Good Laboratory Practices) and safety standards. The ideal candidate will maintain 5S practices, and handle additional responsibilities assigned by the team leader.
Roles & Responsibilities
• You will be responsible for adhering to GLP (Good Laboratory Practices) and safety practices, and ensuring compliance with the SOP (Standard Operating Procedure).
• Your responsibilities include analysis of samples as assigned by the group leader, ensuring adherence to relevant SOPs and Standard Testing Protocols (STPs), and following online documentation and calculation practices.
• You will also be responsible for authorized transactions in SAP and LIMS (Laboratory Information Management System), as well as the online reporting of any Out-of-Specification (OOS), Out-of-Trend (OOT), and incidents to the group leader.
• You will be responsible for verifying that analytical results are conforming with specification limits.
• You will maintain and monitor 5S practices in the laboratory, perform sample management for the team and handle any other responsibilities assigned by the team leader.

Qualifications

Educational qualification: A Bachelor's or master's degree in engineering/ Operations
Minimum work experience: 3 to 7 years of experience in a laboratory setting, preferably in pharmaceutical or related industries
Skills & attributes:
Technical Skills

• Strong understanding and adherence to Good Laboratory Practices (GLP), and knowledge of safety practices.
• Experience in the analysis of samples using analytical techniques.
• Proficiency in online documentation practices, and knowledge of proper calculation practices related to sample analysis.
• Experience in authorized transactions in SAP and LIMS, and familiarity with online reporting systems for OOS, OOT, and incidents.
• Experience in maintaining and monitoring 5S practices in the laboratory.
Behavioural Skills
• Attention to detail in sample analysis and result verification.
• Commitment to cleanliness, order, and organization in the work environment.
• Effective communication skills for reporting incidents and results.
• Ability to work collaboratively in a laboratory team setting.
• Strong organizational skills in managing samples, documentation, and transactions.

Additional Information

About the Department
Global Manufacturing Organisation (GMO)

At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry.
We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities.
Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future.
Benefits Offered
At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs.
The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.
Our Work Culture
Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic.
For more details, please visit our career website at https://careers.drreddys.com/#!/ 

The Company
HQ: Hyderabad, Telangana
0 Employees
On-site Workplace
Year Founded: 1984

What We Do

We accelerate access to affordable and innovative medicines because Good Health Can’t Wait.

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