{"schemaVersion":"jobsearcher.job.v1","id":"c6d5e2ca9dd744a800b9696a","url":"https://jobsearcher.com/jobs/c6d5e2ca9dd744a800b9696a","canonicalUrl":"https://jobsearcher.com/jobs/c6d5e2ca9dd744a800b9696a","title":"Sr. Associate Engineer - Process Development","description":"Yoh presents an excellent long-term Sr. Associate Engineer – Process Development opportunity with a trusted, long-term client located in Waltham, MA .\n\nThis position is part of a major pharmaceutical company , and requires a Bachelors and/or Masters of Science and 1-2+ years of relevant experience . Schedule is full-time M-F (7am-8am start time, 8 hour shift) and may require flexibility to work some evenings and overtime due to projects.\n\nKey Responsibilities\n\nProvide technical support for scale-up and manufacturing issues and develop solutions to improve process efficiency and product quality.\n\nScale-up\n\nPerform process scale-up and Pilot batches\n\nGenerate and execute scale down models for GMP manufacturing\n\nGenerate scale-down models to assist with process scale-up\n\nSolution Development\n\nGenerate process changes to address process issues\n\nLead and assist implementation of Digital Tools\n\nAssist with the implementation and use of digital tools for inventory management, genealogy, and sample submission\n\nAssist with the implementation and use of digital tools for process data acquisition (Electronic lab notebooks and Electronic Batch Records.)\n\nAssist with project activities for the design and technology transfer of mRNA manufacturing processes by contributing and reviewing of Batch Records/Master Production Records (MBR) and Standard Operating Procedures (SOPs).\n\nTech Transfer\n\nAssist with Tech Transfer batches\n\nSupport knowledge packages for Tech Transfer\n\nDocument Generation\n\nAssist with the review MBRs\n\nAssist with the review SOPs\n\nTroubleshoot process/analytical issues that occur during scale-ups and/or in production of drug substance and drug product.\n\nContact vendors for equipment support\n\nConduct investigations using techniques such as 5 why’s, Fishbone diagrams, etc.\n\nDetermine the root cause of process/analytical issues\n\nDevelop solutions to process/analytical issues\n\nEffectively communicate with cross functional teams like Analytical Development, R&D, Process Development, Quality Assurance (QA), Project Management, Regulatory Affairs and Legal teams.\n\nProvide Samples to AD\n\nObtain data from AD and compile into reports\n\nObtain processes from R&D and PD and implement at-scale\n\nGenerate procedures (SOPs, MBRs, Protocols) and work with QA on review and approval\n\nReview and follow QA procedures\n\nAssist in the preparation of technical reports and presentations that support scale-up activities and process improvements.\n\nTechnical reports\n\nGenerate/review Technical reports such as batch summaries, process descriptions, Tech transfer, etc.\n\nPresentations\n\nPresent on batch performance, technical issues, etc.\n\nQualifications\n\n1+ (Masters) or 2+ (Bachelors) years of relevant experience is required\n\nA Bachelor’s degree and/or Master’s degree in Chemical engineering, Biomedical engineering or related field.\n\nDemonstrated experience in process development, manufacturing, tech transfer, and/or scale-up to support the manufacturing of biopharmaceuticals (1+ year) is required\n\nExperience with mRNA Drug Substance is strongly preferred\n\nEstimated Min Rate: $35.00\n\nEstimated Max Rate: $42.00\n\nBenefits\nBenefits include:\n\nMedical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)\n\nHealth Savings Account (HSA) (for employees working 20+ hours per week)\n\nLife & Disability Insurance (for employees working 20+ hours per week)\n\nMetLife Voluntary Benefits\n\nEmployee Assistance Program (EAP)\n\n401K Retirement Savings Plan\n\nDirect Deposit & weekly epayroll\n\nReferral Bonus Programs\n\nCertification and training opportunities\n\nNote: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.\n\nYoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.\n\nVisit https://www.yoh.com/applicants-with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process.\n\nFor California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.\n\nIt is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.\n\nBy applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice: https://www.yoh.com/privacy-notice\n\n#J-18808-Ljbffr","company":"Yoh","rawCompany":"yoh","city":"Waltham","state":"MA","isRemote":false,"isActive":true,"createdAt":"2026-06-18T03:23:52.923Z","occupations":[{"code":"17-2041.00","title":"Chemical Engineers","slug":"chemical-engineers"},{"code":"17-2199.00","title":"Engineers, All Other","slug":"engineers-all-other"},{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"}],"industries":[{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Sr. Associate Engineer - Process Development","description":"Yoh presents an excellent long-term Sr. Associate Engineer – Process Development opportunity with a trusted, long-term client located in Waltham, MA .\n\nThis position is part of a major pharmaceutical company , and requires a Bachelors and/or Masters of Science and 1-2+ years of relevant experience . Schedule is full-time M-F (7am-8am start time, 8 hour shift) and may require flexibility to work some evenings and overtime due to projects.\n\nKey Responsibilities\n\nProvide technical support for scale-up and manufacturing issues and develop solutions to improve process efficiency and product quality.\n\nScale-up\n\nPerform process scale-up and Pilot batches\n\nGenerate and execute scale down models for GMP manufacturing\n\nGenerate scale-down models to assist with process scale-up\n\nSolution Development\n\nGenerate process changes to address process issues\n\nLead and assist implementation of Digital Tools\n\nAssist with the implementation and use of digital tools for inventory management, genealogy, and sample submission\n\nAssist with the implementation and use of digital tools for process data acquisition (Electronic lab notebooks and Electronic Batch Records.)\n\nAssist with project activities for the design and technology transfer of mRNA manufacturing processes by contributing and reviewing of Batch Records/Master Production Records (MBR) and Standard Operating Procedures (SOPs).\n\nTech Transfer\n\nAssist with Tech Transfer batches\n\nSupport knowledge packages for Tech Transfer\n\nDocument Generation\n\nAssist with the review MBRs\n\nAssist with the review SOPs\n\nTroubleshoot process/analytical issues that occur during scale-ups and/or in production of drug substance and drug product.\n\nContact vendors for equipment support\n\nConduct investigations using techniques such as 5 why’s, Fishbone diagrams, etc.\n\nDetermine the root cause of process/analytical issues\n\nDevelop solutions to process/analytical issues\n\nEffectively communicate with cross functional teams like Analytical Development, R&D, Process Development, Quality Assurance (QA), Project Management, Regulatory Affairs and Legal teams.\n\nProvide Samples to AD\n\nObtain data from AD and compile into reports\n\nObtain processes from R&D and PD and implement at-scale\n\nGenerate procedures (SOPs, MBRs, Protocols) and work with QA on review and approval\n\nReview and follow QA procedures\n\nAssist in the preparation of technical reports and presentations that support scale-up activities and process improvements.\n\nTechnical reports\n\nGenerate/review Technical reports such as batch summaries, process descriptions, Tech transfer, etc.\n\nPresentations\n\nPresent on batch performance, technical issues, etc.\n\nQualifications\n\n1+ (Masters) or 2+ (Bachelors) years of relevant experience is required\n\nA Bachelor’s degree and/or Master’s degree in Chemical engineering, Biomedical engineering or related field.\n\nDemonstrated experience in process development, manufacturing, tech transfer, and/or scale-up to support the manufacturing of biopharmaceuticals (1+ year) is required\n\nExperience with mRNA Drug Substance is strongly preferred\n\nEstimated Min Rate: $35.00\n\nEstimated Max Rate: $42.00\n\nBenefits\nBenefits include:\n\nMedical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)\n\nHealth Savings Account (HSA) (for employees working 20+ hours per week)\n\nLife & Disability Insurance (for employees working 20+ hours per week)\n\nMetLife Voluntary Benefits\n\nEmployee Assistance Program (EAP)\n\n401K Retirement Savings Plan\n\nDirect Deposit & weekly epayroll\n\nReferral Bonus Programs\n\nCertification and training opportunities\n\nNote: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.\n\nYoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.\n\nVisit https://www.yoh.com/applicants-with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process.\n\nFor California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.\n\nIt is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.\n\nBy applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice: https://www.yoh.com/privacy-notice\n\n#J-18808-Ljbffr","datePosted":"2026-06-18T03:23:52.923Z","dateModified":"2026-06-18T03:23:52.923Z","hiringOrganization":{"@type":"Organization","name":"Yoh","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Waltham","addressRegion":"MA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"c6d5e2ca9dd744a800b9696a"},"url":"https://jobsearcher.com/jobs/c6d5e2ca9dd744a800b9696a"}}