Join a team of passionate pharmaceutical scientists, formulation experts, and quality professionals shaping the future of preventive healthcare and advanced wellness formulations.
At Ranjauly Health Care, we believe that world-class pharmaceutical products are born from a culture that values scientific rigor, continuous learning, and individual integrity. Operating from our advanced manufacturing campus in UPSIDC Selaqui, Dehradun, our workplace is engineered to foster curiosity, precision, and cross-functional collaboration across every level of our organization.
We cultivate an environment of uncompromised quality where every team member from formulation research scientists and analytical chemists to production engineers is empowered to take ownership, challenge conventional processes, and uphold zero-defect cGMP benchmarks. Open dialogue and transparent leadership ensure that innovative ideas are quickly evaluated, refined, and translated into tangible pharmaceutical advancements.
Our shared commitments that empower each team member to excel, lead, and advance their professional journey.
We believe in lifelong learning. From hands-on training on advanced cGMP automated machinery to evolving global pharmacopeial standards, our team members are empowered to continuously upgrade their skills and technical expertise.
We foster an environment where thoughtful ideas and analytical curiosity are celebrated. Every scientist and engineer is encouraged to take initiative, explore new formulation challenges, and make impactful decisions.
Teamwork and mutual respect are the cornerstone of our operations. We work in complete synergy across R&D, production, QA/QC, and logistics, fostering an inclusive workplace where every contribution is recognized.
Join our multidisciplinary team of scientists, technicians, and manufacturing specialists in Selaqui, Dehradun.
Responsible for in-process quality assurance (IPQA) in solid dosage manufacturing, review of batch manufacturing records (BMR/BPR), change control, deviation logging, and ensuring strict adherence to WHO-GMP norms.
Lead laboratory scale and pilot batch formulation development for advanced nutraceuticals, multivitamins, and modified-release tablets. Experience in stability studies, excipient compatibility, and regulatory dossiers.
Oversee high-throughput rapid mixer granulators (RMG), fluid bed dryers (FBD), and 27-station double rotary compression presses. Ensure batch yield optimization, line clearance, and cGMP compliance.