{"schemaVersion":"jobsearcher.job.v1","id":"cfc97c0d3c2bfe7f5c92e563","url":"https://jobsearcher.com/jobs/cfc97c0d3c2bfe7f5c92e563","canonicalUrl":"https://jobsearcher.com/jobs/cfc97c0d3c2bfe7f5c92e563","title":"Process Development Scientist","description":"Be the First to Apply Division Piramal Pharma Solutions\nPiramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.\nJob Title: Process Development Scientist Location: HPAPI Research and Manufacturing facility, located in Riverview, Michigan.\nResponsibilities Develop, conduct, and/or manage the process development of current and new synthetic/process pathways including routine analytical testing to monitor process progress (HPLC, NMR, XRPD, GC-HS, KF, etc.).\nHandling of highly potent compounds and experience in synthesis and handling of Linker-Payloads is highly desirable.\nScale-up preparative HPLC purification and lyophilization of intermediates and final products.\nMaintain communications with clients and ensure their requirements are met.\nManage/support the production of new (HP)APIs.\nEnsure that adequate supplies of process materials (raw materials, solvents, reagents, etc.) and operation equipment (hoses, reactors, glassware, etc.) are available for assigned tasks.\nEnsure that product shipments meet customer and regulatory (FDA, EPA, OSHA, etc.) requirements.\nWrite progress reports and provide technical support in meetings regarding current API production and new API process development.\nEnsure that approved processes are carried out according to cGMP guidelines and are properly documented.\nKeep Quality Assurance and Quality Control departments updated in regard to project/client requirements and schedules.\nParticipate in the development, training, and transfer of new processes into the plant.\nMaintain accurate inventories of materials.\nPrepare appropriate reports as needed for management and/or clients.\nMaintain notebooks for research and development and non-GMP activities.\nComplete and audit production and cleaning records.\nComplete logbooks and documentation (dispensing record, BPRs, cleaning records, deviation reports, etc.) related to production and cleaning in accordance with regulatory requirements.\nGenerate and/or evaluate standard operating procedures as required.\nProvide technical support for chemical operators, engineering, quality control, etc.\nEducation / Experience PhD in Organic or Medicinal Chemistry and up to four (4) years’ experience in a relevant field; OR MS in Organic or Medicinal Chemistry and up to eight (8) years’ experience in a relevant field; OR BS in Organic or Medicinal Chemistry and up to twelve (12) years’ experience in a relevant field.\nKnowledge of organic chemistry and chemical safety.\nExcellent organizational and planning skills.\nStrong written, verbal, and interpersonal communication skills.\nSelf-motivated, creative, and independent.\nAbility to direct projects covering a variety of chemical compounds including high potent APIs.\nFamiliarity with cGMP, plant safety, and EPA requirements.\nEqual Employment Opportunity Statement PPL provides equal employment opportunities to all employees and applicants for employment. It prohibits discrimination and harassment based on race, color, age, sex, religion, national origin or ethnicity, disability status, genetics, protected veteran status, sexual orientation, gender identity, or expression, or any other characteristic protected by applicable law. Our employment decisions are based on merit considering qualifications, skills, performance, and achievements. Equal employment opportunity applies to all terms and conditions of employment, including recruitment, selection, training, social programs, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions.\n\n#J-18808-Ljbffr","company":"Ppl Pharma Solutions Riverview","rawCompany":"ppl pharma solutions riverview","city":"Riverview","state":"MI","isRemote":false,"isActive":false,"createdAt":"2026-06-22T03:15:44.987Z","occupations":[{"code":"19-2031.00","title":"Chemists","slug":"chemists"},{"code":"17-2041.00","title":"Chemical Engineers","slug":"chemical-engineers"},{"code":"19-4031.00","title":"Chemical Technicians","slug":"chemical-technicians"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325998","title":"All Other Miscellaneous Chemical Product and Preparation Manufacturing","slug":"all-other-miscellaneous-chemical-product-and-preparation-manufacturing"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Development Scientist","description":"Be the First to Apply Division Piramal Pharma Solutions\nPiramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.\nJob Title: Process Development Scientist Location: HPAPI Research and Manufacturing facility, located in Riverview, Michigan.\nResponsibilities Develop, conduct, and/or manage the process development of current and new synthetic/process pathways including routine analytical testing to monitor process progress (HPLC, NMR, XRPD, GC-HS, KF, etc.).\nHandling of highly potent compounds and experience in synthesis and handling of Linker-Payloads is highly desirable.\nScale-up preparative HPLC purification and lyophilization of intermediates and final products.\nMaintain communications with clients and ensure their requirements are met.\nManage/support the production of new (HP)APIs.\nEnsure that adequate supplies of process materials (raw materials, solvents, reagents, etc.) and operation equipment (hoses, reactors, glassware, etc.) are available for assigned tasks.\nEnsure that product shipments meet customer and regulatory (FDA, EPA, OSHA, etc.) requirements.\nWrite progress reports and provide technical support in meetings regarding current API production and new API process development.\nEnsure that approved processes are carried out according to cGMP guidelines and are properly documented.\nKeep Quality Assurance and Quality Control departments updated in regard to project/client requirements and schedules.\nParticipate in the development, training, and transfer of new processes into the plant.\nMaintain accurate inventories of materials.\nPrepare appropriate reports as needed for management and/or clients.\nMaintain notebooks for research and development and non-GMP activities.\nComplete and audit production and cleaning records.\nComplete logbooks and documentation (dispensing record, BPRs, cleaning records, deviation reports, etc.) related to production and cleaning in accordance with regulatory requirements.\nGenerate and/or evaluate standard operating procedures as required.\nProvide technical support for chemical operators, engineering, quality control, etc.\nEducation / Experience PhD in Organic or Medicinal Chemistry and up to four (4) years’ experience in a relevant field; OR MS in Organic or Medicinal Chemistry and up to eight (8) years’ experience in a relevant field; OR BS in Organic or Medicinal Chemistry and up to twelve (12) years’ experience in a relevant field.\nKnowledge of organic chemistry and chemical safety.\nExcellent organizational and planning skills.\nStrong written, verbal, and interpersonal communication skills.\nSelf-motivated, creative, and independent.\nAbility to direct projects covering a variety of chemical compounds including high potent APIs.\nFamiliarity with cGMP, plant safety, and EPA requirements.\nEqual Employment Opportunity Statement PPL provides equal employment opportunities to all employees and applicants for employment. It prohibits discrimination and harassment based on race, color, age, sex, religion, national origin or ethnicity, disability status, genetics, protected veteran status, sexual orientation, gender identity, or expression, or any other characteristic protected by applicable law. Our employment decisions are based on merit considering qualifications, skills, performance, and achievements. Equal employment opportunity applies to all terms and conditions of employment, including recruitment, selection, training, social programs, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions.\n\n#J-18808-Ljbffr","datePosted":"2026-06-22T03:15:44.987Z","dateModified":"2026-06-22T03:15:44.987Z","hiringOrganization":{"@type":"Organization","name":"Ppl Pharma Solutions Riverview","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Riverview","addressRegion":"MI","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"cfc97c0d3c2bfe7f5c92e563"},"url":"https://jobsearcher.com/jobs/cfc97c0d3c2bfe7f5c92e563"}}