SMT Technical Trainee at Dr Reddy's Laboratories Limited

Bollaram, Telangana, India -

Full Time

Start Date

Immediate

Expiry Date

02 May, 26

Salary

0.0

Posted On

01 Feb, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Process Design, Experiment Execution, Data Interpretation, Clean Room Practices, Safety Guidelines, Calibration, Batch Production Record, Quality Testing, Documentation Control, Analytical Methods, Team Player, Communication Skills, Self-Starter, Pharmaceutical Process, Formulation Development, Risk-Based Approaches

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 Job Summary We are seeking a dynamic Technical Trainee to provide inputs in process design/ selection of process based on product understanding. Design and execute experiments with relevant documentation, interpret data from experiment etc. Roles & Responsibilities 1.1. To perform all operations in Production area (intermediate area and clean room area) in accordance to the established SOPs and cGMP and capture the data in relevant documents. 1.2. To follow the Clean Room practices as per defined SOPs. 1.3. Maintain the good Housekeeping in production area and around the concerned Production area. 1.4. To operate the equipment safely by following Safety guidelines and wearing the P PE during the execution of production activities. 1.5. Maintain and calibrate the measuring devices in the concerned production area. 1.6. Ensure the gauges, transmitter etc. calibrations, and equipment's preventive maintenance before executing the Batches. 1.7. To procure Raw materials from Ware house. 1.8. Carry out the operations according to the Batch Production Record, Equipment & Area Cleaning Record. 1.9. To enter/ensure the batch related details (Stan time, input, output etc.) in SAP. 1.10. To execute batches (Trial/ Process Performance Qualification / Commercial etc.) as per the Production planning schedule. 1.11. To arrange for Quality testing of in-process, intermediate & finished goods as per SOP. 1.12. To handover the shift details / activities perfectly to the next shift person. 1.13. To update the stocks. 1.14. To raise a maintenance work request for Production block maintenance activities. 1.15. To report any near miss incidents to the concerned department and report the Process / System deviations to Quality Assurance through a relevant document and to involve, investigate and implement the corrective actions. 1.16. Handover relevant documents to Quality Assurance within the stipulated timeline as per SOP. 1.17. To verify and perform the operations in DCS/PLC as per SOP and take print parameter record sheets from DCS/PLC and attach to respective batch production record. 1.18. To complete the Assigned trainings in Talent Hub. 1.19. To attend the cGMP & Safety training and intemal training classes. 1.20. Verify the production documents & records and ensure the Good documentation practices & documentation control, archival destruction are following as per SOP. 1.21. To ensure safety & cGMP related documents are maintained in place for the reference of production team. 1.22. To undertake any other job as may be assigned by the concerned production in-charge / Department Head (Production). Qualifications Educational qualification- Intermediate/Diploma Minimum work experience- Fresher/ 0-3 years of Experience Skills & attributes Technical Skills- • Displays basic understanding on criteria for API attributes, dosage form, patents. • Demonstrates understanding of pharmaceutical process designing and selection (based on Critical process parameters), QbD concepts & risk-based approaches for process optimization as well as ability to prepare technical protocols, reports and Technical write up. Good knowledge of small scale and large-scale equipment with great understanding of scale up calculation. • Knowledge of ICH guidelines related to Product development or Process Development. • Formulation Development-Demonstrates understanding of execution methodology (based on Critical material Attributes, Critical Quality Attributes of products), & evaluation of dosage forms for desired attributes (e.g. dissolution time, impurities). • Analytical Research-Demonstrates preferred understanding of the basic analytical methods. Behavioural Skills- • Self-starter • Team player • Excellent oral and written communication skill. Additional Information About the Department Integrated Product Development Organisation We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) & Other dosages Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years. 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/#!/ Job Family: Early Careers Sub Job Family: Technical_Track Preferred type of working: On-Premise Years of Experience: 0 - 1 Business unit: GMO

Responsibilities

The Technical Trainee will perform operations in the production area according to established SOPs and cGMP, ensuring data capture and maintaining good housekeeping. They will also operate equipment safely, procure raw materials, execute batches, and ensure quality testing.