Analytical Specialist

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 seeking a highly skilled Analytical Scientist in to join our Research and Development team for Injectable and Inhalations Division for developing and validating analytical methods for injectable products Inhalation products Nasal products ensuring compliance with the regulatory requirements conducting literature reviews scaling up for manufacturing of batches coordinating manufacturing readiness overseeing plant execution and facilitating seamless technology transfer This role demands a strong understanding of analytical principles excellent documentation skills and the ability to work effectively in a collaborative team environment scaling up for manufacturing of batches coordinating manufacturing readiness overseeing plant execution and facilitating seamless technology transfer Roles ResponsibilitiesYou will be responsible Analytical method development and validation of injectable Inhalations and Nasal products You will be responsible to perform the Drug Master File Literature review and procure the relevant columns and standards in order to initiate the analytical method development Stay updated with the latest literature and industry developments in the field You will be responsible to execute analytical activities as per defined procedures document the data and send the respective record of analysis to group leader analytical expert for the review and release in order to provide the approved results to formulation team You will be responsible for analytical method development for drug products for various tests mentioned in the specification in order to analyse the product development batches for the prototype screening You will be responsible for analytical method validation activities at the manufacturing sites providing method development reports to verify the validation parameters and ensure the execution of method validation as per the regulatory requirement in order to provide the authentic analytical validation report for the regulatory filing You will be responsible for analytical method transfer to plant locations successfully in order to train the Quality Control QC team on the methods for the Exhibit and commercial batch analysis at plant You will be responsible to ensure proper maintenance of laboratory equipment as per Good Laboratory Practices GLP standards to guarantee accurate and reliable results You will be responsible to calibrate instruments as per the calibration schedule and strictly follow Standard Operating Procedures SOPs to maintain consistency and accuracy You will be responsible to maintain a clean and organized work area and ensure that the laboratory environment is controlled at the required temperature for optimal analytical conditions You will be responsible to keep all relevant documents well-maintained and organized for easy access and compliance with internal and external auditing requirements QualificationsEducational qualification Masters in Science Organic chemistry Pharmaceutical SciencesMinimum work experience 10 years of experience in analytical method developmentSkills attributes Technical Skills Have work experience on Process scale up of Inhalation Nasal and Injectable Products Have work experience on Formulation Development and expertise in inhalation injectable dosage form Understanding on Abbreviated New Drug Application ANDA filing requirements Experience in Process Optimization Manufacturing and Technology Transfer Strong understanding of regulatory guidelines and industry standards related to pharmaceutical product development and analysis Proven experience in method validation and documentation in compliance with regulatory requirements Behavioral Skills Excellent communication and interpersonal skills Strong analytical and problem-solving abilities Ability to work collaboratively with own team and cross-functional teams Additional InformationAbout the DepartmentIntegrated Product Development OrganisationWe 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