{"schemaVersion":"jobsearcher.job.v1","id":"4a1dddd79ffb99e2b1402920","url":"https://jobsearcher.com/jobs/4a1dddd79ffb99e2b1402920","canonicalUrl":"https://jobsearcher.com/jobs/4a1dddd79ffb99e2b1402920","title":"Process Development Scientist/Engineer","description":"1 month ago Be among the first 25 applicants\nJD243\nJob Title: Process Development Scientist/Engineer 1\nDepartment: Process Development & Technical Operations\nReports to: Manager, Product & Process Development & Quality Control\nLocation: Bloomington, IN (Onsite)\nPosition Type: Full-time, 40 hours/week, Exempt\n\nGeneral Responsibilities:\n1. Support the Product and Process Development department as a technical transfer liaison and technical writer on parenteral drug product manufacturing projects.\n2. Stays current with bodies of knowledge, identifying best practices, regulatory requirements, industry standards and trends.\n3. Share knowledge gained with Singota employees.\n4. Identify process improvements and support planning and implementation.\n5. Author, edit, review, and execute procedures and protocols.\n6. Assist in authoring Batch Records and Specification sheets for Formulation, Filling, Inspection and Finishing.\n7. Collaborate in writing and responding to deviations, investigations, and corrective actions.\n8. Maintains knowledge of and performs functions in compliance with laws and regulations including\nbut not limited to Company’s policies and standard operating procedures, FDA and similar regulatory authorities.\n9. Positive Attitude and willingness to work as part of a diverse team to achieve overall goals of the company.\n10. Comply with quality and safety management systems including requirements for documentation, training, system use, SOPs, processes, and procedures. Ensure procedures are followed and changed if no longer applicable.\n11. General support required of a company where everyone is expected to perform multiple tasks both inside and outside their department to meet the needs of the business.\n12. Operational knowledge of Cytiva/Vanrx SA25 or other robotic filling isolator is a plus.\n\nRequirements\n\nSkills and Physical Activity Requirements:\n1. Able to support the client team in organizing and leading meetings, and driving projects to meet operational deliverables.\n2. Proficient with electronic systems, including but not limited to enterprise resource planning (ERP), and Microsoft Office applications, particularly Word, Excel, PowerPoint and Project.\n3. Trustworthiness and personal integrity – able to maintain a high degree of confidentiality\n4. Strong verbal, listening and written communication skills.\n5. Good time management and organizational skills.\n6. Positive attitude and good judgment.\n7. Customer focused both to internal staff and external clients.\n8. Proficient math and chemistry skills required including knowledge of manufacturing methods.\n\nEducation Requirements:\n1. Bachelor’s degree in a scientific discipline and 2+ years’ experience in pharma industry, formulation and aseptic manufacturing experience preferred\nOr\n2. Associates degree in a scientific discipline and 4+ years’ experience in a pharma industry, formulation and aseptic manufacturing experience required\n\nBenefits\n\nDental insurance - effective day one of employment\n\nHealth insurance - effective day one of employment\n\nVision insurance - effective day one of employment\n\nHealth savings account\n\nLife insurance\n\nPaid time off\n\nTuition reimbursement\n\n401(k)\n\n401(k) matching\n\nSingota Solutions is an Equal Opportunity Employer\n\nSeniority level Seniority level Mid-Senior level\nEmployment type Employment type Full-time\nJob function Job function Science\nIndustries Pharmaceutical Manufacturing\nReferrals increase your chances of interviewing at Singota Solutions by 2x\nGet notified about new Process Development Scientist jobs in Bloomington, IN .\nWe’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.\n\n#J-18808-Ljbffr","company":"Singota Solutions","rawCompany":"singota solutions","city":"Bloomington","state":"IN","isRemote":false,"isActive":false,"createdAt":"2026-07-16T03:14:51.352Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2041.00","title":"Chemical Engineers","slug":"chemical-engineers"},{"code":"41-4011.00","title":"Sales Representatives, Wholesale and Manufacturing, Technical and Scientific Products","slug":"sales-representatives-wholesale-and-manufacturing-technical-and-scientific-products"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-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/Engineer","description":"1 month ago Be among the first 25 applicants\nJD243\nJob Title: Process Development Scientist/Engineer 1\nDepartment: Process Development & Technical Operations\nReports to: Manager, Product & Process Development & Quality Control\nLocation: Bloomington, IN (Onsite)\nPosition Type: Full-time, 40 hours/week, Exempt\n\nGeneral Responsibilities:\n1. Support the Product and Process Development department as a technical transfer liaison and technical writer on parenteral drug product manufacturing projects.\n2. Stays current with bodies of knowledge, identifying best practices, regulatory requirements, industry standards and trends.\n3. Share knowledge gained with Singota employees.\n4. Identify process improvements and support planning and implementation.\n5. Author, edit, review, and execute procedures and protocols.\n6. Assist in authoring Batch Records and Specification sheets for Formulation, Filling, Inspection and Finishing.\n7. Collaborate in writing and responding to deviations, investigations, and corrective actions.\n8. Maintains knowledge of and performs functions in compliance with laws and regulations including\nbut not limited to Company’s policies and standard operating procedures, FDA and similar regulatory authorities.\n9. Positive Attitude and willingness to work as part of a diverse team to achieve overall goals of the company.\n10. Comply with quality and safety management systems including requirements for documentation, training, system use, SOPs, processes, and procedures. Ensure procedures are followed and changed if no longer applicable.\n11. General support required of a company where everyone is expected to perform multiple tasks both inside and outside their department to meet the needs of the business.\n12. Operational knowledge of Cytiva/Vanrx SA25 or other robotic filling isolator is a plus.\n\nRequirements\n\nSkills and Physical Activity Requirements:\n1. Able to support the client team in organizing and leading meetings, and driving projects to meet operational deliverables.\n2. Proficient with electronic systems, including but not limited to enterprise resource planning (ERP), and Microsoft Office applications, particularly Word, Excel, PowerPoint and Project.\n3. Trustworthiness and personal integrity – able to maintain a high degree of confidentiality\n4. Strong verbal, listening and written communication skills.\n5. Good time management and organizational skills.\n6. Positive attitude and good judgment.\n7. Customer focused both to internal staff and external clients.\n8. Proficient math and chemistry skills required including knowledge of manufacturing methods.\n\nEducation Requirements:\n1. Bachelor’s degree in a scientific discipline and 2+ years’ experience in pharma industry, formulation and aseptic manufacturing experience preferred\nOr\n2. Associates degree in a scientific discipline and 4+ years’ experience in a pharma industry, formulation and aseptic manufacturing experience required\n\nBenefits\n\nDental insurance - effective day one of employment\n\nHealth insurance - effective day one of employment\n\nVision insurance - effective day one of employment\n\nHealth savings account\n\nLife insurance\n\nPaid time off\n\nTuition reimbursement\n\n401(k)\n\n401(k) matching\n\nSingota Solutions is an Equal Opportunity Employer\n\nSeniority level Seniority level Mid-Senior level\nEmployment type Employment type Full-time\nJob function Job function Science\nIndustries Pharmaceutical Manufacturing\nReferrals increase your chances of interviewing at Singota Solutions by 2x\nGet notified about new Process Development Scientist jobs in Bloomington, IN .\nWe’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.\n\n#J-18808-Ljbffr","datePosted":"2026-07-16T03:14:51.352Z","dateModified":"2026-07-16T03:14:51.352Z","hiringOrganization":{"@type":"Organization","name":"Singota Solutions","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Bloomington","addressRegion":"IN","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"4a1dddd79ffb99e2b1402920"},"url":"https://jobsearcher.com/jobs/4a1dddd79ffb99e2b1402920"}}