{"schemaVersion":"jobsearcher.job.v1","id":"76bcb266f2cacde9c0bb71f8","url":"https://jobsearcher.com/jobs/76bcb266f2cacde9c0bb71f8","canonicalUrl":"https://jobsearcher.com/jobs/76bcb266f2cacde9c0bb71f8","title":"Sr. Process Engineers - Pharma Technical Services","description":"Job DescriptionOur client – a global and growingBioPharma CDMOcompany needsmultipleProcess Engineers in the Pharma Technical Services group,located at their expanding plant inWA state.Excellent total comp.up to $143K+with excellentBenefits + Relocation Bonus . Client will sponsor forH1B Visa transfer. This is a permanent direct Hire and not a contractor roleJob Posting #2728Job Title :Sr. Process Engineers – Pharma Technical Services Location:Spokane, WA Relocation:YES –The client offers a generous lumpsum bonus for relo assistance. Compensation:Salary range$110K - $130K+Annual Bonus (10 %) Full Benefits:Medical, Vision, Dental,15 days ' vacation/Sick time,10- Holidays,401k(matchup to 4%) . Company Info: Our client is a growing company in the Pharmaceutical Industry. They are a part of a global parent company with sites in many countries with around1,300 peopleat this site inSpokane ,WA. This is an integrated contract development and manufacturing organization(CDMO)offering specializedAseptic Sterile manufacturing, filling and lyophilizationof drug products inVials.Group Info:Be part of thePlant Technical Services Group of around 20 technical staff.This group has2 sections supporting New Product Introductions – NPI & existing commercially manufactured products Note 1:The company recently completed their3rd state-of-the-art Sterile Liquid compounding & Vial Filling lineand are currently expanding again with a4th lineat this growing plant site .Note 2:This is a permanent direct Hire role. The client will transfer existing H1B and support future Green Card applications.Job Summary:TheSenior Process Engineerprovides expertise primarily in the areas of pharmaceutical process engineering and technical transfer.This position will support large scale projects and multi-disciplinary teams. The process engineer will also provide technical direction for complex projects and exhibit superior communication skills with all levels of employees. The individual will be responsible for refining department and site processes and provide leadership and guidance to others. Level Specific Expectations Expected to perform job functions autonomously and effectively.Expected to be an authority in pertinent scientific principles and applicable existing and new guidance. Expected to be an authority on technical aspects of site processes. Expected to provide leadership and guidance to others on these topics, as well as update and improve site practices and policies accordingly.Job Functions Design, optimize, implement manufacturing processes to improve efficiency, quality and sustainability Oversee and assess existing processes and workflows Establish and track process metrics to monitor process stability and discover areas for improvement Technical Transfer of new products from both internal and external clients Ownership of product process from initial quote to product retirement Evaluate incoming processes for robustness, efficiency and fit Perform appropriate development work to define CPPs and CQAs to allow strong execution upon transfer to Manufacturing.Author validation study documents that demonstrate manufacturing processes are capable of consistently making acceptable product. Develop and execute validation studies to test and qualify new and improved manufacturing processes. Troubleshooting, oversight and/or sampling of events within Manufacturing will require occasional off-shift at-location support.Generate reports summarizing results of studies to document data collected; utilize data obtained to qualify site processes Review data summaries generated by other departments, assess the data for potential trends or conditions that may adversely impact the quality of the sterile products being manufactured, and ensure that corrective action measures are implemented whenrequired/warranted. Participate in or perform deviation investigation and evaluation of impact Implement effective CAPAs Provide necessary reviews for regulatory and client audits and provide responses to audit observations In-depth understanding of cGMP's, European regulatory requirements, relevant USP chapters, and scientific principles associated with clean room operations and room classifications as they apply to media fills, sterilization and depyrogenation (dry heat and steam), endotoxin reduction, and microbiological monitoring and control. Candidate Must Have: Bachelorsof Science in Arts or Science or related technical degree. 5+ years of technical servicesexperience in theBioPharmaindustry Technical service experience supporting theexisting commercially manufactured productsorTech Transfer of New Productsfrom Development to Manufacturing. Experience withPharma sterile aseptic manufacturing, filling, Lyophilization Ability towork independentlyin a fast-pacedCDMOenvironment. Candidate Nice to Have: BSinBiology, Chemistry, Physics, or Engineering Advanced degree ( MS Degreecounted as 2 years of experience) Some Leadership,Supervisory experienceover Jr. Engineers, Technicians. SomeTechnical Transfer Project Managementexperience Experience withStatistical Analysis, Lean Manufacturing Experience handlingChange Control and CAPAsituations Ability to grow into aSubject Matter Expert (SME)for Manufacturing & Process unit Operations Process Validation Experience Keywords:Process engineer, technical services, Project Manager, Manufacturing support, Pharma, CDMO, plant, FDA, GMP, Sterile Aseptic liquid filling, contract Manufacturing, Lean Manufacturing, CAPA, Change control, NPI","company":"MRINetwork","rawCompany":"mrinetwork","city":"Spokane","state":"WA","isRemote":false,"isActive":false,"createdAt":"2026-11-10T11:46:05.598Z","occupations":[{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"},{"code":"17-2041.00","title":"Chemical Engineers","slug":"chemical-engineers"},{"code":"17-2199.00","title":"Engineers, All Other","slug":"engineers-all-other"}],"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":"325411","title":"Medicinal and Botanical Manufacturing","slug":"medicinal-and-botanical-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Sr. Process Engineers - Pharma Technical Services","description":"Job DescriptionOur client – a global and growingBioPharma CDMOcompany needsmultipleProcess Engineers in the Pharma Technical Services group,located at their expanding plant inWA state.Excellent total comp.up to $143K+with excellentBenefits + Relocation Bonus . Client will sponsor forH1B Visa transfer. This is a permanent direct Hire and not a contractor roleJob Posting #2728Job Title :Sr. Process Engineers – Pharma Technical Services Location:Spokane, WA Relocation:YES –The client offers a generous lumpsum bonus for relo assistance. Compensation:Salary range$110K - $130K+Annual Bonus (10 %) Full Benefits:Medical, Vision, Dental,15 days ' vacation/Sick time,10- Holidays,401k(matchup to 4%) . Company Info: Our client is a growing company in the Pharmaceutical Industry. They are a part of a global parent company with sites in many countries with around1,300 peopleat this site inSpokane ,WA. This is an integrated contract development and manufacturing organization(CDMO)offering specializedAseptic Sterile manufacturing, filling and lyophilizationof drug products inVials.Group Info:Be part of thePlant Technical Services Group of around 20 technical staff.This group has2 sections supporting New Product Introductions – NPI & existing commercially manufactured products Note 1:The company recently completed their3rd state-of-the-art Sterile Liquid compounding & Vial Filling lineand are currently expanding again with a4th lineat this growing plant site .Note 2:This is a permanent direct Hire role. The client will transfer existing H1B and support future Green Card applications.Job Summary:TheSenior Process Engineerprovides expertise primarily in the areas of pharmaceutical process engineering and technical transfer.This position will support large scale projects and multi-disciplinary teams. The process engineer will also provide technical direction for complex projects and exhibit superior communication skills with all levels of employees. The individual will be responsible for refining department and site processes and provide leadership and guidance to others. Level Specific Expectations Expected to perform job functions autonomously and effectively.Expected to be an authority in pertinent scientific principles and applicable existing and new guidance. Expected to be an authority on technical aspects of site processes. Expected to provide leadership and guidance to others on these topics, as well as update and improve site practices and policies accordingly.Job Functions Design, optimize, implement manufacturing processes to improve efficiency, quality and sustainability Oversee and assess existing processes and workflows Establish and track process metrics to monitor process stability and discover areas for improvement Technical Transfer of new products from both internal and external clients Ownership of product process from initial quote to product retirement Evaluate incoming processes for robustness, efficiency and fit Perform appropriate development work to define CPPs and CQAs to allow strong execution upon transfer to Manufacturing.Author validation study documents that demonstrate manufacturing processes are capable of consistently making acceptable product. Develop and execute validation studies to test and qualify new and improved manufacturing processes. Troubleshooting, oversight and/or sampling of events within Manufacturing will require occasional off-shift at-location support.Generate reports summarizing results of studies to document data collected; utilize data obtained to qualify site processes Review data summaries generated by other departments, assess the data for potential trends or conditions that may adversely impact the quality of the sterile products being manufactured, and ensure that corrective action measures are implemented whenrequired/warranted. Participate in or perform deviation investigation and evaluation of impact Implement effective CAPAs Provide necessary reviews for regulatory and client audits and provide responses to audit observations In-depth understanding of cGMP's, European regulatory requirements, relevant USP chapters, and scientific principles associated with clean room operations and room classifications as they apply to media fills, sterilization and depyrogenation (dry heat and steam), endotoxin reduction, and microbiological monitoring and control. Candidate Must Have: Bachelorsof Science in Arts or Science or related technical degree. 5+ years of technical servicesexperience in theBioPharmaindustry Technical service experience supporting theexisting commercially manufactured productsorTech Transfer of New Productsfrom Development to Manufacturing. Experience withPharma sterile aseptic manufacturing, filling, Lyophilization Ability towork independentlyin a fast-pacedCDMOenvironment. Candidate Nice to Have: BSinBiology, Chemistry, Physics, or Engineering Advanced degree ( MS Degreecounted as 2 years of experience) Some Leadership,Supervisory experienceover Jr. Engineers, Technicians. SomeTechnical Transfer Project Managementexperience Experience withStatistical Analysis, Lean Manufacturing Experience handlingChange Control and CAPAsituations Ability to grow into aSubject Matter Expert (SME)for Manufacturing & Process unit Operations Process Validation Experience Keywords:Process engineer, technical services, Project Manager, Manufacturing support, Pharma, CDMO, plant, FDA, GMP, Sterile Aseptic liquid filling, contract Manufacturing, Lean Manufacturing, CAPA, Change control, NPI","datePosted":"2026-11-10T11:46:05.598Z","dateModified":"2026-11-10T11:46:05.598Z","hiringOrganization":{"@type":"Organization","name":"MRINetwork","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Spokane","addressRegion":"WA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"76bcb266f2cacde9c0bb71f8"},"url":"https://jobsearcher.com/jobs/76bcb266f2cacde9c0bb71f8"}}