Job Description

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.Roles & Responsibilities * To implement GDP as per the Company\'s Quality policy for ESD.

• To ensure that compliance (regulatory, statutory and legal) is understood, implemented and monitored on daily basis.
• Preparation and updating of Job descriptions & organogram of ESD.
• To ensure that the new SOPs, CCFs, Validation protocols, reports (like qualification) etc. (with the support of related peers) are prepared and reviewed and implemented on time as per the ESD objectives.
• Preparation of Equipment qualification protocols and reports. Ensuring timely completion as per schedule.
• Preparation of SOPs and ensuring periodical review.
• Initiating ESD CCFs, IRs, Tracking and closure of CCF, IR and CAPA of ESD.
• Incident investigations and finding root cause of failures with appropriate CAPA.
• To provide Audit support, response & tracking.
• To prepare updated plant layout and P& ID diagrams.
• To ensure maintaining the records on history of equipment at the site.
• To ensure timely documentation as per SOP.
• Making of routine trends, reports, receipts. etc for the ESD department.
• To be involved in pre-audits (relevant to ESD).
• To be involved and ensuring training of ESD personnel as per the site objectives.
• To provide Induction training for new employees.
• Ensure Preventive maintenance of production area and ZLD area instruments.
• Preparation of Preventive and facility maintenance schedules and ensuring completion as per schedule.
• Preparation and tracking of ESD related schedules.
• To maintain records/ documents as per SOPs.
• Ensure that the equipment and related systems (both old and new) are (re)qualified / (re)validated as per schedule.
• To ensure cGMP implementation in his/her area as per the QMS.
• Ensure the good housekeeping as per site objectives.
• To meet SHE targets for their area.
• You will be responsible for reviewing engineering deliverables and extending appropriate corrective actions to attain excellence.
• Your role includes guiding team in closure of event investigation, proposing proper CAPA (Corrective and Preventive Actions) and ensuring audit compliance.
• You will be responsible for handling projects related to machine upgradation, installation and commissioning of new equipment, and area modification.
• You will also manage interactions with vendors, cross-functional teams, regulatory teams and internal audit teams.
• You will be responsible for providing inputs and responses fore deviations and observations during internal audits and inspections.

QualificationsEducational qualification: A bachelor\'s in engineering (Mechanical Engineering or Any other Discipline)Minimum work experience: 5 to 10 yearsSkills & attributes:Technical Skills

• Knowledge on Reactors, centrifuges, AHU\'s, RCVD, Millers, Sifters, Pass box, Vacuum Pumps, Centrifugal Pumps, etc.
• Experience in Ensuring preventive maintenance & Calibration schedules.
• Experience in handling audits, inspections, event investigations and CAPA.
• Basic knowledge on PLC and computerized system (SCADA).

Behavioural skills

• Team management and leadership skills to lead engineering team.
• Commitment to compliance and quality.
• Project management skills to handle equipment modification and installation projects.
• Good communication skills to collaborate with vendors and cross-functional teams and coordinate with regulatory and internal audit teams.

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/#!/

Dr. Reddy\'s Laboratories