{"schemaVersion":"jobsearcher.job.v1","id":"50c19bf12bfedeb8594d61f6","url":"https://jobsearcher.com/jobs/50c19bf12bfedeb8594d61f6","canonicalUrl":"https://jobsearcher.com/jobs/50c19bf12bfedeb8594d61f6","title":"Process Scientist","description":"Process Engineer\nJob Number: 23-00777\nBe part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Process Engineer for our client in Warren, NJ.\nEclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!\nPosition Overview:\nWill play a key role in ensuring successful manufacture of life-saving cell therapy products.\nThe primary focus of the Process Engineer will be to support testing and implementation of operational improvements and resolve manufacturing process investigations at the Client cell therapy GMP manufacturing facility.\nWill be part of a team tasked with determining the root cause of manufacturing investigations.\nThis individual will design and execute experiments, evaluate data and draft technical reports in support of improvement, investigations and manufacturing process changes.\nAlso contribute to well controlled comparability and validation studies which enable regulatory filings for raw material and process changes.\nResponsibilities:\nParticipate in Root Cause Analyses to determine cause of manufacturing process investigations.\nCoordinate with the analytical group for timely delivery of process samples and turn-around of analytical data.\nSupport production related investigations, ensuring compliance with internal standards and regulatory requirements.\nDevelop and execute manufacturing process changes and improvement activities, and/or author technical reports for process changes and improvements.\nSupport process comparability and process validation studies including planning, execution and documentation management.\nSupport necessary technical experiments and analysis to enable decisions related to raw materials changes.\nContributes to ownership and advancement of work processes, and procedures.\nFlexibility with work as maintenance of cell cultures\nRequired Qualifications:\nDegree in Biological Sciences, Chemical Engineering, Life Sciences or related discipline; BS degree with minimum of 7+ years of relevant experience, or MS degree with minimum 5+ years of relevant experience in cell therapy/ biologic process\nSupervisory role, GMP experience\nExperience with cell therapy process development or manufacturing\nGMP experience desirable\nProficiency utilizing MS Office products and working knowledge of statistical software (R, JMP, Minitab)\nExperience executing investigations in support of commercial manufacturing\nExperience with commercial product support, i.e. post-marketing commitments, on-going validation and comparability\nCombination of experience in Development, MSAT and/or quality.\nOperational excellence training/background\nJob Type: Contract\nPay: $55.00 - $61.00 per hour\nSchedule:\n10 hour shift\n12 hour shift\nWork Location: On the road","company":"Eclaro","rawCompany":"eclaro","city":"Hackettstown","state":"NJ","isRemote":false,"isActive":false,"createdAt":"2026-08-06T11:27:39.738Z","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":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Scientist","description":"Process Engineer\nJob Number: 23-00777\nBe part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Process Engineer for our client in Warren, NJ.\nEclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!\nPosition Overview:\nWill play a key role in ensuring successful manufacture of life-saving cell therapy products.\nThe primary focus of the Process Engineer will be to support testing and implementation of operational improvements and resolve manufacturing process investigations at the Client cell therapy GMP manufacturing facility.\nWill be part of a team tasked with determining the root cause of manufacturing investigations.\nThis individual will design and execute experiments, evaluate data and draft technical reports in support of improvement, investigations and manufacturing process changes.\nAlso contribute to well controlled comparability and validation studies which enable regulatory filings for raw material and process changes.\nResponsibilities:\nParticipate in Root Cause Analyses to determine cause of manufacturing process investigations.\nCoordinate with the analytical group for timely delivery of process samples and turn-around of analytical data.\nSupport production related investigations, ensuring compliance with internal standards and regulatory requirements.\nDevelop and execute manufacturing process changes and improvement activities, and/or author technical reports for process changes and improvements.\nSupport process comparability and process validation studies including planning, execution and documentation management.\nSupport necessary technical experiments and analysis to enable decisions related to raw materials changes.\nContributes to ownership and advancement of work processes, and procedures.\nFlexibility with work as maintenance of cell cultures\nRequired Qualifications:\nDegree in Biological Sciences, Chemical Engineering, Life Sciences or related discipline; BS degree with minimum of 7+ years of relevant experience, or MS degree with minimum 5+ years of relevant experience in cell therapy/ biologic process\nSupervisory role, GMP experience\nExperience with cell therapy process development or manufacturing\nGMP experience desirable\nProficiency utilizing MS Office products and working knowledge of statistical software (R, JMP, Minitab)\nExperience executing investigations in support of commercial manufacturing\nExperience with commercial product support, i.e. post-marketing commitments, on-going validation and comparability\nCombination of experience in Development, MSAT and/or quality.\nOperational excellence training/background\nJob Type: Contract\nPay: $55.00 - $61.00 per hour\nSchedule:\n10 hour shift\n12 hour shift\nWork Location: On the road","datePosted":"2026-08-06T11:27:39.738Z","dateModified":"2026-08-06T11:27:39.738Z","hiringOrganization":{"@type":"Organization","name":"Eclaro","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Hackettstown","addressRegion":"NJ","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"50c19bf12bfedeb8594d61f6"},"url":"https://jobsearcher.com/jobs/50c19bf12bfedeb8594d61f6"}}