{"schemaVersion":"jobsearcher.job.v1","id":"e76f5cdc5c414ea8fa3563cd","url":"https://jobsearcher.com/jobs/e76f5cdc5c414ea8fa3563cd","canonicalUrl":"https://jobsearcher.com/jobs/e76f5cdc5c414ea8fa3563cd","title":"Process Engineer","description":"Process Engineer/Scientist required to work within the Process Development Commercial Support team based in Amgen Dun Laoghaire (ADL). The team is responsible for providing process and product support to drug product formulation and fill-finish operations in ADL as drug product process SMEs\n\nKey responsibilities:\nDay-to-day operations support as a subject matter expert in drug product formulation, vial filling, pre-filled syringe filling, lyophilization and vial capping.\nKey contributor to product and process investigations, responsible for assessing product and process impact.\nLeads continuous improvement projects to improve process performance and productivity.\nTypical activities include the following (but not exclusively):\nAssess product impact associated with proposed changes to commercial processes under the change control process.\nGenerate product impact assessments associated with process excursions and deviations, with reference to product technical documentation.\nSupport new product introduction team, as a process subject matter expert; This would include but is not limited to, recipe development and protocol execution, as well as troubleshooting and investigation support.\nReview and approve changes to operating procedures, electronic batch records, and product documentation.\nRisk assessments and mitigation projects relating to line performance.\nPerform process gap analysis and developing strategies to close gaps.\nData trend analysis for all performance aspects of the area.\nTroubleshooting performance trends.\n\nThe chosen candidate will work in a collaborative manner within the process teams structure and contribute as a member of cross functional teams within the local organization and functional team globally.\n\nBasic Qualifications:\n• Bachelor’s or Masters degree in Engineering, Science or related discipline with 6 years experience in a similar role OR PhD and 3 years of directly related experience.\n• Demonstrated leadership skills with the ability to build teams and operate across functional boundaries, both internal and external.\n\nPreferred Qualifications:\n• Typically 4-6 years drug product experience in areas such as drug product formulation, vial/pre-filled syringe filling or lyophilisation\n• Qualification in Lean and 6-sigma methodologies would be an advantage.\n• New product introduction (NPI), process development, MSAT experience in a GMP environment would be advantageous.\n\n#LI-GH1\n#Contract","company":"Hyde Engineering Consulting","rawCompany":"hyde engineering consulting","city":"Denver","state":"CO","isRemote":false,"isActive":false,"createdAt":"2026-08-15T12:36:59.774Z","occupations":[{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"},{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2041.00","title":"Chemical Engineers","slug":"chemical-engineers"}],"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 Engineer","description":"Process Engineer/Scientist required to work within the Process Development Commercial Support team based in Amgen Dun Laoghaire (ADL). The team is responsible for providing process and product support to drug product formulation and fill-finish operations in ADL as drug product process SMEs\n\nKey responsibilities:\nDay-to-day operations support as a subject matter expert in drug product formulation, vial filling, pre-filled syringe filling, lyophilization and vial capping.\nKey contributor to product and process investigations, responsible for assessing product and process impact.\nLeads continuous improvement projects to improve process performance and productivity.\nTypical activities include the following (but not exclusively):\nAssess product impact associated with proposed changes to commercial processes under the change control process.\nGenerate product impact assessments associated with process excursions and deviations, with reference to product technical documentation.\nSupport new product introduction team, as a process subject matter expert; This would include but is not limited to, recipe development and protocol execution, as well as troubleshooting and investigation support.\nReview and approve changes to operating procedures, electronic batch records, and product documentation.\nRisk assessments and mitigation projects relating to line performance.\nPerform process gap analysis and developing strategies to close gaps.\nData trend analysis for all performance aspects of the area.\nTroubleshooting performance trends.\n\nThe chosen candidate will work in a collaborative manner within the process teams structure and contribute as a member of cross functional teams within the local organization and functional team globally.\n\nBasic Qualifications:\n• Bachelor’s or Masters degree in Engineering, Science or related discipline with 6 years experience in a similar role OR PhD and 3 years of directly related experience.\n• Demonstrated leadership skills with the ability to build teams and operate across functional boundaries, both internal and external.\n\nPreferred Qualifications:\n• Typically 4-6 years drug product experience in areas such as drug product formulation, vial/pre-filled syringe filling or lyophilisation\n• Qualification in Lean and 6-sigma methodologies would be an advantage.\n• New product introduction (NPI), process development, MSAT experience in a GMP environment would be advantageous.\n\n#LI-GH1\n#Contract","datePosted":"2026-08-15T12:36:59.774Z","dateModified":"2026-08-15T12:36:59.774Z","hiringOrganization":{"@type":"Organization","name":"Hyde Engineering Consulting","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Denver","addressRegion":"CO","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"e76f5cdc5c414ea8fa3563cd"},"url":"https://jobsearcher.com/jobs/e76f5cdc5c414ea8fa3563cd"}}