Team Leader

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 Adhere to the company safety norms policies and procedures Adhere to the SOP s and other laid down procedures of Block- A Production Injectable packing water system area To ensure effective implementation of Company policies and procedures in the department To ensure that products are produced and stored according to the appropriate documentation in order to obtain the required quality Planning of routine activities in production injectable department To Review the instructions 01 SCP s SOP s etc relating to production Injectable operations and to ensure their implementation To ensure that the production records are evaluated and signed by an authorized person before they are sent to the Quality Assurance Department To check the maintenance of area and equipment in the department To review Validation Qualification Documents and all related reports as per requirement To ensure that the required initial and periodic training of department personnel is completed as per the schedule To ensure that manufacturing area environment and water quality test results are within limit as per requirement Review of area environmental monitoring trends and water quality trends To ensure personnel hygiene of department personnel To ensure that appropriate equipment qualification process validations are performed as per requirement To ensure that periodic training programme is followed as per the schedule and evaluation is done as per requirement Ensuring appropriate storage conditions of materials and products Monitoring of compliance to current Good Manufacturing Practices Inspection investigation and taking of samples as appropriate in order to monitor factors which may affect product quality and to make provision for taking new products To ensure that material indents are done as per the requirement and to review and approve the purchase indents for department Participate and review of Risk Assessments To attend inventory production planning meeting and accordingly ensure proper material and production Injectable packing and water system planning Responsible for Dispensing of Raw material from ware house To coordinate with the Research and development team for planning and execution of the Exhibit batches in the production Injectable and OSD department To review approve related quality notifications To ensure that all changes incidents deviations are reported evaluated investigated and the conclusions are made as per requirement To ensure the up keep of the production Injectable packing water system and oral solid dosage forms equipment s and area Ensure completion of Periodic review revision of GMP documents as per requirement To ensure that process lead time and product yields are as per requirement Manpower planning and work allocation for production Injectable packing water system and oral solid dosage forms personnel To ensure the smooth coordination with other related departments - Warehouse HR Admin Engineering services QA QC TTG and SHE To review the market complaints in coordination with Quality Assurance Department and taking the required corrective and preventive actions Preparation and review of BMR BPR URS and all other GMP records as per requirement To ensure timely completion of all the GMP records in the department Participate and review of Risk Assessments To ensure timely completion of calibration preventive maintenance activities of production Injectable packing and water system equipment s To perform on - line entries in GMP documents like BMR s BPR s log- books etc as per Good Documentation practice To coordinate with engineering department to reduce production break down time and ensure proper rectification of the problems occurred To participate in self inspection audit team as per schedule Scheduling and Execution of periodic media fill batches as per requirement To maintain the discipline in the department and to recommend actions if any Meeting the production targets on time To raise the quality notification and breakdown as and when required and closure of the same To maintain the Daily Production Report Control of the incidents and unusual observation by close monitoring of the operations Ensuring process and systems in place for operations and continuous improvement To review performance appraisal of team To perform any other task project assigned by Head Operations To perform the duties of Designee for Head Production whenever production head is absent Responsible for co-ordination of SATT To participate and perform task of site investigation team 2 0 Delegation of Activities 1 In absence of role holder Team leader will perform the roleTo ensure that the appropriate qualifications validations calibrations are done as per requirementQualificationsEducational qualification MSC M PharmacyMinimum work experience 8 to 12 yearsBehavioural skills Leadership skills to plan allocate tasks and supervise production personnel fostering teamwork and ensuring adherence to safety norms and quality standards Effective communication skills to coordinate with various departments ensuring seamless collaboration and alignment of activities Capacity to identify and address production-related issues promptly initiate corrective and preventive actions and facilitate investigations and CAPA closure to minimize disruptions and improve processes Strong organizational skills to plan routine activities prioritize tasks and ensure timely completion of calibration preventive maintenance production planning and other operational activities Commitment to maintaining current regulatory compliance and adherence to norms to uphold product quality and safety standards 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