(High Salary) Process Engineer

Company DescriptionDr 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 transparencyDr 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 Summary We are looking for a Team Member Process Engineering in MSAT for coordinating preventive maintenance schedules overseeing external contractors and ensuring compliance with safety and quality standards They review production operations train team members manage spare parts inventory and lead troubleshooting efforts to minimize downtime Additionally they maintain budgets support technical activities and ensure regulatory compliance contributing to the efficient and reliable operation of equipment and facilities Roles Responsibilities You will be responsible for overseeing all operations in accordance with established SOPs protocols and any cGMP documents ensuring data is captured in relevant documents following Good Documentation Practices You will be responsible for performing risk analysis before implementing any changes in the production area to mitigate potential hazards or disruptions You will be responsible for ensuring assimilation qualification and validation of new processes or technologies in production documenting and sharing findings with relevant team members You will be responsible for improving yields solvent recovery waste reduction and other production objectives to enhance operational efficiency You will be responsible for initiating and closing change control action plans to manage modifications effectively within the production environment You will be responsible for enhancing quality in both process and finished goods through continuous improvement initiatives You will be responsible for investigating incidents out-of-specification OOS out-of-trend OOT occurrences and complaints to identify root causes and implement corrective actions You will be responsible for troubleshooting issues to ensure process robustness aiming to find permanent solutions for operational challenges You will be responsible for ensuring that all site objectives for Safety Health and Environment SHE are met maintaining a safe working environment You will be responsible for reviewing batch production records batch cleaning records electronic batch production records e-BPRs and electronic batch control records e-BCRs for compliance and accuracy You will be responsible for preparing and reviewing Process Performance Qualification PPQ protocols reports Continued Process Verification CPV protocols reports and Batch Production Records BPRs for existing products undergoing changes You will be responsible for ensuring that trial recommendations are accurately captured in the validation batch production record for operational convenience and compliance You will be responsible for adhering to established cGMP and safety protocols during all operations reporting any deviations or incidents promptly You will be responsible for reporting near-miss accidents to the appropriate Production Superior for investigation and corrective action You will be responsible for documenting and reporting process system deviations to Quality Assurance QA participating in investigations and implementing corrective actions as necessary You will be responsible for executing and monitoring the commercialization of Critical Process Parameters CPP processes to ensure consistency and quality in production You will be responsible for attending mandatory training classes on cGMP SOPs process and operational safety to maintain compliance and competency You will be responsible for verifying temperature tuning completion before starting up trials or validation batches to ensure process integrity and accuracy QualificationsEducational qualification Bachelors in Engineering or a related fieldMinimum work experience 5-7 years of experience in the pharmaceutical industry with a focus on manufacturing and engineering Skills attributes Technical Skills Proficiency in supporting manufacturing and delivery processes incident investigation and CAPA Corrective Preventive Action implementation Strong understanding of process safety principles and risk assessment methodologies Experience in driving continuous improvement initiatives to enhance quality capacity and productivity Behavioural skills Attention to detail and strong organizational skills Ability to work collaboratively in a cross-functional team environment Excellent communication and interpersonal skills Additional InformationAbout 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