{"schemaVersion":"jobsearcher.job.v1","id":"65d6f3f0b086bae22f8cfda0","url":"https://jobsearcher.com/jobs/65d6f3f0b086bae22f8cfda0","canonicalUrl":"https://jobsearcher.com/jobs/65d6f3f0b086bae22f8cfda0","title":"Associate Scientist I/II, Formulation & Process Development","description":"Associate Scientist I/II, Formulation & Process Development\nWeston, FL\nCategory: R&D and Manufacturing Process Scale-up\nType: Full-time\nMin. Experience: Some Experience\n\nPosition Summary\nIn this role, the Associate Scientist I/II will provide hands-on formulation and process expertise during the development of clinical and commercial formulations for orally inhaled and nasal drug products (OINDPs). Conducts laboratory activities including formulation and manufacturing process development, manufacturing process scale-up and process transfer activities across equipment, manufacturing scales and sites. The individual will design and execute formulation experiments, organize and analyze results with minimal supervision, and communicate data and interpretation to product development team. Contribute towards the development of orally inhaled and nasal drug products (OINDPs) by following regulatory guidelines, industry best practices, US FDA cGMPs, and other relevant guidelines.\nEssential Duties and Responsibilities\nConducts standard and advanced laboratory activities including formulation development and manufacturing process development, manufacturing process scale-up and process transfer activities across equipment, manufacturing scales and sites.\nConducts manufacture of lab scale R&D, pilot scale, pivotal scale and commercial scale batches by following written documentation.\nWorks independently to determine methods and techniques on new or difficult assignments related to research, formulation and process development and manufacturing activities.\nDemonstrates technical proficiency, scientific creativity, collaboration with others and independent thought in suggesting experimental design and research strategy.\nInterfaces with Quality Assurance and Compliance, to ensure that work is being performed and documented according to established procedures.\nPlans and designs new testing methodologies to assess the performance of new product formulations.\nContribute towards development of orally inhaled and nasal drug products (OINDPs) by following regulatory guidelines, industry best practices, US FDA cGMPs, and other relevant guidelines.\nDocument and report all laboratory and manufacturing activities according to cGMPs and Transpire Bio’s SOPs.\nWork and communicate effectively with other functional groups and across global respiratory R&D sites.\nEstablish and maintain effective relationships with team members.\nConduct lab work in accordance with SOPs; follow Transpire Bio safety rules and procedures.\nComply with all Transpire Bio Corporate guidelines and policies.\n\nRequired Qualifications\nBSc in Chemistry, Pharmacy or related fields with at least 3 years of experience in Pharmaceutical R&D\nMSc in Chemistry, Pharmacy or related fields with 0-2 years of experience in Pharmaceutical R&D\nExperience in the formulation, process development and/or manufacture of injectables, ophthalmic, and other sterile products is preferred.\nThe ability to embrace a highly multi-disciplinary collaborative approach and work independently is essential.\nAdaptable and flexible, readily adapts to change & new projects.\nEngineering/Science background with knowledge of product development processes\nQuick learner and ability to think critically\nAbility to pay special attention to detail with degree of accuracy.\nExcellent interpersonal, organizational and communication skills.\nStrong written and verbal communication skills are required.\n\nWhy Join Us?\nWe are a fast-growing pharmaceutical startup dedicated to innovation and improving patient outcomes. Join us to gain hands-on experience in a growing pharmaceutical business, get exposure to various functions with opportunities for career development and work in a collaborative and supportive work environment.","company":"Transpire Bio","rawCompany":"transpire bio","city":"Weston","state":"FL","isRemote":false,"isActive":false,"createdAt":"2026-05-11T06:16:43.950Z","occupations":[{"code":"41-4011.00","title":"Sales Representatives, Wholesale and Manufacturing, Technical and Scientific Products","slug":"sales-representatives-wholesale-and-manufacturing-technical-and-scientific-products"},{"code":"19-1042.00","title":"Medical Scientists, Except Epidemiologists","slug":"medical-scientists-except-epidemiologists"},{"code":"11-9121.00","title":"Natural Sciences Managers","slug":"natural-sciences-managers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"541715","title":"Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)","slug":"research-and-development-in-the-physical-engineering-and-life-sciences-except-nanotechnology-and-biotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Associate Scientist I/II, Formulation & Process Development","description":"Associate Scientist I/II, Formulation & Process Development\nWeston, FL\nCategory: R&D and Manufacturing Process Scale-up\nType: Full-time\nMin. Experience: Some Experience\n\nPosition Summary\nIn this role, the Associate Scientist I/II will provide hands-on formulation and process expertise during the development of clinical and commercial formulations for orally inhaled and nasal drug products (OINDPs). Conducts laboratory activities including formulation and manufacturing process development, manufacturing process scale-up and process transfer activities across equipment, manufacturing scales and sites. The individual will design and execute formulation experiments, organize and analyze results with minimal supervision, and communicate data and interpretation to product development team. Contribute towards the development of orally inhaled and nasal drug products (OINDPs) by following regulatory guidelines, industry best practices, US FDA cGMPs, and other relevant guidelines.\nEssential Duties and Responsibilities\nConducts standard and advanced laboratory activities including formulation development and manufacturing process development, manufacturing process scale-up and process transfer activities across equipment, manufacturing scales and sites.\nConducts manufacture of lab scale R&D, pilot scale, pivotal scale and commercial scale batches by following written documentation.\nWorks independently to determine methods and techniques on new or difficult assignments related to research, formulation and process development and manufacturing activities.\nDemonstrates technical proficiency, scientific creativity, collaboration with others and independent thought in suggesting experimental design and research strategy.\nInterfaces with Quality Assurance and Compliance, to ensure that work is being performed and documented according to established procedures.\nPlans and designs new testing methodologies to assess the performance of new product formulations.\nContribute towards development of orally inhaled and nasal drug products (OINDPs) by following regulatory guidelines, industry best practices, US FDA cGMPs, and other relevant guidelines.\nDocument and report all laboratory and manufacturing activities according to cGMPs and Transpire Bio’s SOPs.\nWork and communicate effectively with other functional groups and across global respiratory R&D sites.\nEstablish and maintain effective relationships with team members.\nConduct lab work in accordance with SOPs; follow Transpire Bio safety rules and procedures.\nComply with all Transpire Bio Corporate guidelines and policies.\n\nRequired Qualifications\nBSc in Chemistry, Pharmacy or related fields with at least 3 years of experience in Pharmaceutical R&D\nMSc in Chemistry, Pharmacy or related fields with 0-2 years of experience in Pharmaceutical R&D\nExperience in the formulation, process development and/or manufacture of injectables, ophthalmic, and other sterile products is preferred.\nThe ability to embrace a highly multi-disciplinary collaborative approach and work independently is essential.\nAdaptable and flexible, readily adapts to change & new projects.\nEngineering/Science background with knowledge of product development processes\nQuick learner and ability to think critically\nAbility to pay special attention to detail with degree of accuracy.\nExcellent interpersonal, organizational and communication skills.\nStrong written and verbal communication skills are required.\n\nWhy Join Us?\nWe are a fast-growing pharmaceutical startup dedicated to innovation and improving patient outcomes. Join us to gain hands-on experience in a growing pharmaceutical business, get exposure to various functions with opportunities for career development and work in a collaborative and supportive work environment.","datePosted":"2026-05-11T06:16:43.950Z","dateModified":"2026-05-11T06:16:43.950Z","hiringOrganization":{"@type":"Organization","name":"Transpire Bio","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Weston","addressRegion":"FL","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"65d6f3f0b086bae22f8cfda0"},"url":"https://jobsearcher.com/jobs/65d6f3f0b086bae22f8cfda0"}}