10 Preformulation Studies Jobs

Role Overview: As an intern at ThinQ Pharma, you will be responsible for assisting in formulation and pre-formulation studies, supporting the development of stability and bio batches, maintaining lab records including BMR/BPR and SOPs, coordinating with cross-functional teams such as QA/QC/Production, and performing basic lab tests with a focus on accurate data recording. Key Responsibilities: - Assist in formulation and pre-formulation studies - Support the development of stability and bio batches - Maintain lab records including BMR/BPR and SOPs - Coordinate with cross-functional teams such as QA/QC/Production - Perform basic lab tests with a focus on accurate data recording Qualifications...

Role Overview As a Senior Executive - Formulation Development at Lambda Therapeutics & Research Limited, you will be responsible for the development and optimization of pharmaceutical drug formulations. Your role will involve performing pre-formulation studies, scaling up processes, conducting stability studies, ensuring compliance with regulatory guidelines, and collaborating with cross-functional teams for project success. Key Responsibilities - Develop and optimize pharmaceutical drug formulations - Perform pre-formulation studies - Scale up processes - Conduct stability studies - Ensure compliance with regulatory guidelines - Collaborate with cross-functional teams Qualification Required...

As a Formulation Design & Development Scientist, your role will involve designing and developing robust, scalable formulations for oral solid dosage forms (OSDs) such as tablets, capsules, and granules. You will be responsible for selecting appropriate excipients, processing techniques (e.g., direct compression, wet/dry granulation), and equipment. Your key responsibilities will include: - Developing formulations that align with target product profiles (QTPP), ensuring considerations for bioavailability, stability, and manufacturability. - Conducting pre-formulation studies to assess properties like solubility, hygroscopicity, flow, and compressibility. - Performing drug-excipient compatibil...

As a Scientist in Pharmaceutical Development, you will be responsible for planning and executing various tasks related to the development, scale up, and manufacturing of drug products for monoclonal antibodies (mAb), bi-specific, tri-specific antibodies, and Antibody Drug Conjugates (ADC) of New biological entities (NBE). Your key responsibilities will include: - Significant experience in development, scale up, and manufacturing of drug products for mAbs, ADCs, etc. - Experience in parenteral delivery systems development like Nanoparticulate delivery systems, Lipid based delivery systems. - Proficient in pre-formulation studies of mAbs and ADCs along with physiochemical & Solid-State charact...

As an intern at ThinQ Pharma, you will have the opportunity to be involved in various aspects of pharmaceutical research and development. Your role will include the following responsibilities: - 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. - 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 ...

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, troublesh...

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 ...

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...

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...

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 pr...