(Urgent Search) Team Member Cleaning Validation- Manufacturing Science

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 Summary We are looking for a detail-oriented individual to lead the implementation of cleaning validation procedures and protocols ensuring compliance with regulatory standards and Good Manufacturing Practices GMP This role involves preparing and reviewing SOPs validation plans and reports contributing significantly to the quality management system and regulatory compliance efforts within the organization Roles Responsibilities You will be responsible for preparation review and approval of Cleaning Master Validation Plan Cleaning Validation and Verification Protocols and Reports Acceptance Criteria documents Cleaning Validation matrix and Periodic Monitoring Schedule You will be responsible for implementing and complying with the cleaning validation SOP Standard Operating Procedure and the Cleaning Validation master plan You will assist in preparation and review of SOP Operating Instruction Standard Cleaning Procedure Your responsibilities include compiling cleaning validation reports by summarizing reported data updating periodic monitoring schedule as required and providing support in identifying hard-to-clean locations and deriving surface area for contact parts You will track and manage execution of cleaning validation activity You will also review and approve QMS Quality Management System documents such as incidence reports change controls etc You will be accountable for ensuring that validation activities are carried out according to the protocol and in compliance with cGMP Current Good Manufacturing Practices cGxP Current Generally Accepted Practices and regulatory requirements Your role extends to assisting preparation and review of risk assessments URS User Requirement Specification and Design Qualification documents related to cleaning validation activities You will be expected to participate in internal and external audits providing explanations of cleaning validation related documents to auditors and inspection teams You will be responsible for QMS management including initiation approval and closure of change controls incidents audit compliance and impact assessment For all cleaning validation related activities your role involves providing support to internal and external stakeholders providing training to personnel and participating in digitalization and simplification of activities Qualifications Qualifications Educational qualification Bachler of pharmacy master s in science pharmacy Minimum work experience 3-7 years of experience in Cleaning Validation Skills attributes Technical Skills Experience in the execution of cleaning validation activities for products in Solid dosage forms Experience in Swab sampling activities Ability to prepare technical protocols and reports Experience in risk assessment approaches Knowledge of PDA Tech report 29 ISPE APIC and other relevant guidelines Familiarity and proficiency in using CLEEN software Experience in Analytical Research and knowledge on interpretation of the data Behavioural Skills Excellent communication and interpersonal skills Strong analytical and problem-solving abilities Performance oriented and good at building leveraging relationship Ability to work collaboratively with own team and cross-functional teams Committed to Learning Coaching the team Additional Information About the Department IPDO 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