5 Preformulation Studies Jobs

As a Research Associate at Naari Pharma, you will play a crucial role in the execution of formulation development activities for solid dosage forms across regulated and semi-regulated markets. Your responsibilities will include conducting literature search and pre-formulation studies, evaluating innovator/RLD products, executing R&D trial batches and scale-up activities, and preparing stability batches. You will also be responsible for documentation tasks such as preparing Master Formula Cards, Product Development Reports, and Stability Protocols, as well as supporting regulatory submissions. You will work closely with cross-functional teams to monitor scale-up and exhibit batches, troubleshoot formulation challenges, and ensure adherence to development timelines and project goals. The ideal candidate for this position should hold an M. Pharma degree in Pharmaceutics, have at least 3 years of hands-on experience in solid dosage formulation development, possess knowledge of pre-formulation, DoE, and scale-up activities, and be familiar with stability studies and regulatory documentation. Strong problem-solving skills, attention to detail, and good communication and teamwork abilities are also essential for this role. If you are passionate about advancing women's health through pharmaceutical innovation and are looking for an opportunity to contribute to a global company with a focus on hormonal therapies, we encourage you to apply for the Research Associate position at Naari Pharma.,

As an Intern in CMC (Formulation) at Ferring India FHPDC R&D, you will be part of the CMC (Formulation) department in Hyderabad for a duration of 12 months. Reporting to the Lead Scientist - CMC (Formulation), you will receive a stipend for your work. To qualify for this position, you should have a Masters degree in Pharmaceutical Sciences (Pharmaceutics) or a related discipline from a reputable institution. A strong academic background in pharmaceutics is essential, along with basic knowledge of formulation principles and analytical techniques. Familiarity with regulatory guidelines such as ICH, FDA, and EMA is advantageous. Proficiency in MS Office (Word, Excel, PowerPoint) and scientific writing, as well as excellent communication, organizational, and problem-solving skills, are required. Your role as a Formulation R&D Intern will involve supporting the development of pharmaceutical dosage forms through hands-on laboratory work, data analysis, and documentation. You will gain exposure to formulation science, regulatory requirements, and industrial practices in a dynamic and collaborative environment. Key responsibilities include assisting in the design and optimization of formulations for various dosage forms, conducting pre-formulation studies, participating in excipient selection, preparing lab-scale and pilot-scale batches, operating laboratory equipment, maintaining accurate documentation, ensuring compliance with Good Laboratory Practices (GLP), collaborating with other departments such as Analytical R&D, Quality Control, and Regulatory Affairs, and contributing to formulation strategy discussions. This internship offers a unique opportunity to enhance your skills and knowledge in the field of CMC (Formulation) while working in a supportive and innovative environment at Ferring India FHPDC R&D.,

The ideal candidate for this position will join our R&D/F&D team focusing on Oral Solid Dosage (OSD) forms, including pellets and tablets. You will be responsible for conducting pre-formulation and formulation development studies, process validation, stability studies, and technology transfer of new pharmaceutical products while ensuring adherence to ICH guidelines and internal SOPs. Your key responsibilities will include conducting detailed literature reviews to support new product development initiatives. You will evaluate reference products, patents, regulatory status, and formulation strategies. Additionally, you will perform physicochemical characterization of API and excipients, assess compatibility, solubility, and stability as part of pre-formulation studies. In the formulation development phase, you will design and develop robust formulations for tablets and pellets. You will optimize process parameters through laboratory and pilot-scale trials. Stability studies will be conducted following ICH guidelines and internal SOPs, where you will interpret results and recommend necessary formulation or process adjustments. You will coordinate and execute process validation batches in the production department, ensuring compliance with GMP and validation protocols. Technology transfer responsibilities will include preparing and reviewing complete technology transfer documentation (TTD) and facilitating successful scale-up and handover of developed products to manufacturing. In case of troubleshooting, you will provide technical support for commercialized products to resolve formulation or process issues. Documentation and record-keeping tasks will involve preparing and updating Product Development Files (PDF), Product Logbooks, and Instrument Logbooks regularly. Additionally, you will draft and review documents such as QAQN (Quality Assessment & Qualification Note), MFR (Master Formula Record), and FPS (Finished Product Specification). Qualifications required for this position include a B.Pharm/M.Pharm in Pharmaceutics or Pharmaceutical Technology and 13 years of relevant experience in F&D/R&D, preferably in OSD (tablets/pellets) formulation development in a regulated environment.,

As an intern at ThinQ Pharma, your day-to-day responsibilities will involve assisting in formulation and pre-formulation studies, supporting the development of stability and bio batches, helping in maintaining lab records including BMR/BPR and SOPs, coordinating with cross-functional teams such as QA/QC/Production, and performing basic lab tests while ensuring accurate data recording. ThinQ Pharma is an integrated pharmaceutical company with a strong global presence and a reputation for offering world-class products and services. Headquartered in Singapore and operating a fully equipped research center in Mumbai, India, ThinQ Pharma has been a key player in the global market for more than 25 years. With a highly skilled team, the company is committed to providing comprehensive solutions for the pharmaceutical and wellness industries.,

As a bench scientist in our organization, you will be responsible for conducting experimentation and research in the area of formulation development, process development, regulatory affairs, and intellectual property for global markets. Your work will involve planning and executing experiments aligned with project milestones while applying scientific principles such as Quality by Design (QbD), Design of Experiments (DoE), statistics, and scale-up principles. You will be expected to analyze and interpret data from literature reviews effectively to support decision-making processes. Additionally, you will need to understand the intellectual property landscape, develop strategies, search for prior art, and establish proof of concept through experimentation. Collaboration with cross-functional teams including Manufacturing Science and Technology (MS&T), Quality Assurance (QA), Quality Control (QC), and production teams across different geographies will be crucial for technology transfer and timely execution of submission batches. Your role will also involve identifying challenges, bottlenecks in development, and providing mitigation proposals at various stages of product development. Furthermore, you will be responsible for problem-solving, prioritizing activities, conducting development trials, and ensuring alignment with established milestones. Clear communication with internal stakeholders, proactive identification of challenges or risks, and adherence to business unit Key Performance Indicators (KPIs) will be essential aspects of your role. On a day-to-day basis, you will work closely with the formulation development teams to achieve key milestones, conduct experiments following QbD principles, and prepare presentations at different stages of product development. Your tasks will include literature reviews, sourcing API and Excipients, conducting preformulation studies, executing development trials, interpreting analytical data, and preparing necessary documentation for regulatory submissions. To be successful in this role, you should hold a Ph.D. in Pharmaceutical Sciences with at least 1 year of experience or an M.Pharm in Pharmaceutical Sciences with a minimum of 3 years of experience from reputable universities. Prior experience in working with generic pharmaceuticals in regulated markets such as the US, EU, or Canada will be advantageous. Your commitment to personal accountability, effective work habits, continuous learning, and collaboration with internal teams will be instrumental in contributing to the success of our organization's mission to make good health more affordable and accessible globally.,