About this role
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
Roles & Responsibilities
- Responsible for preparing necessary documents before experiments, including calculations for working stocks and reagent preparations, data templates, etc. Ensuring the availability of prerequisites (reagents and information) before executing experiments for the smooth execution of the given experiment.
- Executing experiments with minimized technical errors, according to defined Standard Operating Procedures (SOP) and development plans in compliance with safety and quality norms. Ensuring the generation of high-quality data and meeting project requirements as defined by the supervisor.
- Contemporaneous, accurate, legible, attributable, and original data documentation of day-to-day execution. Adhering to the organization's quality management system and ensuring data reproducibility.
- Identifying and notifying the supervisor of any out-of-trend data and being involved in writing SOP/SDP (Standard Documentation Procedure)/any work instruction documents.
Qualifications
Educational qualification and work experience
Educational qualification: A Graduation or Post Graduation in Science, including Pharma and Technology
Minimum work experience: 3 to 8 years of Academic or Industrial experience
Skills & attributes
Technical Skills
- Basic understanding of relevant techniques, including cell-based and ligand binding assays. Familiarity with fundamental biotechnology industry practices.
- Understanding of protein-protein interactions, encompassing principles of ELISA (Enzyme-Linked Immunosorbent Assay), electrophoresis, and western blotting techniques.
- Knowledge of animal cell culture techniques, including the handling, maintenance, and propagation of cell lines.
Behavioural skills
- Learning orientation, seeking opportunities for personal and professional development.
- Stakeholder orientation, focusing on understanding and meeting the needs of various stakeholders involved.
- Ability to build relationships, fostering positive connections with colleagues, clients, and other stakeholders.
"
Additional Information
About the Department
Biologics
Currently operates in the Global Biosimilars business - a segment that is poised for attractive and sustained growth over the next 10–15-year time horizon...
" Benefits Offered
At Dr. Reddy’s, we actively help to catalyze your career growth and professional development through personalized learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards...
" 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...
For more details, please visit our career website at https://careers.drreddys.com/#!/
"
Other facts
About Dr Reddy's Laboratories Limited
Established in 1984, we are a global pharmaceutical company headquartered in Hyderabad, India. Driven by our purpose of ‘Good Health Can’t Wait’, we work to provide access to affordable and innovative medicines. We offer a portfolio of products and services including APIs, generics, branded generics, biosimilars and OTC. Our major markets include USA, India, Russia & CIS countries, China, Brazil and Europe. As a company with a history of deep science that has led to several industry firsts, we continue to plan ahead and invest in future growth drivers such as access to novel molecules, digital therapeutics and consumer healthcare. As an early adopter of sustainability and ESG actions, we released our first Sustainability Report in 2004. Our current ESG goals aim to set the bar high in environmental stewardship; access and affordability for patients; diversity; and governance. For more information, log on to: www.drreddys.com.
Caution Notice: Dr. Reddy's has been made aware of candidates receiving fraudulent job opportunities from unauthorised recruiting agencies or people impersonating Dr. Reddy's leaders. These fraudulent jobs may be advertised on employment sites or mimic our careers site and company email addresses. Please know that Dr. Reddy's Laboratories has no affiliation or connection to these situations. Dr. Reddy's (and its associated/group companies) follows a formal recruitment process through its own HR department. Please report immediately in case you suspect a fraudulent job. You may raise your concern by:
Accessing https://drreddys.ethicspoint.com.
Calling on the hotline number. List of hotline numbers are available in https://drreddys.ethicspoint.com. The hotline is available 24x7 in multiple languages.
Writing to [email protected] or [email protected].
For our community guidelines on LinkedIn, please visit: https://shorturl.at/LTvNZ
What you'll do
- The Analytical Quality Assurance Associate is responsible for preparing documents and ensuring the availability of prerequisites for experiments. They execute experiments according to SOPs, ensuring high-quality data generation and compliance with safety and quality norms.
Ready to join Dr Reddy's Laboratories Limited?
Take the next step in your career journey