Team Member - QC CTO

Dr. Reddy's Laboratories

India
Permanent
Full-time

15 days ago

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 DescriptionJob Summary
We are looking for a meticulous individual to support in LC-MS and GC-MS analysis, ensuring precise identification and quantification of nitrosamine impurities in pharmaceutical products. Your role will involve performing sample analysis, method development, validation, and equipment calibration, all pivotal for maintaining accuracy, reliability, and adherence to safety and cGLP guidelines.Roles & Responsibilities

You will be responsible for supporting team lead in conducting LC-MS (Liquid Chromatography - Mass Spectrometry) and GC-MS (Gas Chromatography - Mass Spectrometry) analysis to identify and quantify nitrosamine impurities in API (Active Pharmaceutical Ingredient) and Finished Dosage Form, ensuring compliance with regulatory standards.
You will be responsible for performing sample analysis according to approved procedures, maintaining accuracy and precision in results.
You will be responsible for aiding in literature surveys and developing HPLC (High-Performance Liquid Chromatography) and GC (Gas Chromatography) methods for API and Finished Dosage Form, ensuring robustness and reliability.
You will be responsible for executing method validations following approved protocols to validate analytical methods for accuracy, precision, specificity, and robustness.
You will be responsible for performing calibration of analytical equipment as per SOP to maintain accuracy and reliability of results.
You will be responsible for supporting team lead in preparation of analytical documents such as specifications and standard testing procedures (STPs).
You will be responsible for adhering to safety and cGLP (Current Good Lab Practices) guidelines, following relevant SOPs (Standard Operating Procedures), and conducting equipment usage and maintenance as per procedures to maintain a safe working environment.

QualificationsEducational qualification: An M.Sc. degree in Chemistry, Analytical Chemistry, or a related fieldMinimum work experience: 3 to 6 yearsSkills & attributes:Technical Skills

Sound knowledge of NMR (Nuclear Magnetic Resonance) data interpretation and proficiency in preparing structure elucidation reports to support analytical findings.
Knowledge of calibration and performance verification of analytical instruments and equipment as per the master schedule.
Good understanding of advanced instrumentation technique skills.
Experience in ensuring the maintenance, preparation, and procurement of laboratory standards, chemicals, and solvents according to established procedures.
Participation and organization of equipment/instrument qualifications and change control mechanisms.
Procurement expertise for laboratory requirements.

Behavioural skills

Attention to detail and commitment to ensuring compliance with QMS (Quality Management System) documents, including OOS (Out-of-Specification), OOT (Out-of-Trend), and Incident investigations.
Ability to respond to internal and external audits and participate in other QMS-related activities.
Strong organizational skills for LIMS (Lab Information Management System) related activities.
Effective communication and collaboration skills for coordinating and implementing of SOPs.

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

Apply Now