AQA Associate at Dr Reddy's Laboratories Limited

Hyderabad, Telangana, India -

Full Time

Start Date

Immediate

Expiry Date

13 May, 26

Salary

0.0

Posted On

12 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Cell-based Assays, Ligand Binding Assays, Elisa, Electrophoresis, Western Blotting, Animal Cell Culture, Data Documentation, Sop Writing, Quality Management System, Learning Orientation, Stakeholder Orientation, Relationship Building

Industry

Pharmaceutical Manufacturing

Description

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 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 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/#!/ Job Family: Quality Sub Job Family: Quality Assurance Preferred type of working: On-Premise Business unit: Biologics

Responsibilities

The role involves preparing necessary experimental documents, ensuring the availability of reagents and information, and executing experiments according to SOPs while adhering to safety and quality norms. Responsibilities also include generating high-quality data, maintaining accurate documentation, and notifying supervisors of any out-of-trend data.