Process Development Associate – Process Engineering & Sterile Manufacturing

Quick CV Drop OffFirst NameThis is a required fieldLast NameThis is a required fieldEmail AddressA valid email address is required This is a required fieldTelephone NumberThis is a required fieldJob Type3" title="Job Type" name="cvjobtypes" data-req="Required" data-isselected="false"> -- Please Select -- Contract PermanentThis is a required fieldCV UploadChoose FileYou can only upload files up to 10 MB in size You can only upload doc, docx or pdf files This is a required fieldI confirm that I have read and agree with Orion Group's Terms & Conditions, Privacy Policy & Cookie PolicyThis is a required fieldBack to resultsProcess Development Associate – Process Engineering & Sterile ManufacturingApply NowTR/083210 Posted: 24/07/2026$20 - $23 per hourUnited States, Illinois, North Chicago Contract Process Development Associate – Process Engineering & Sterile ManufacturingLocation: Hybrid – North Chicago/Lake County, IL 60064Contract: 1 year, with potential for extensionSchedule: Monday–Friday, standard business hoursPay: $20–$23/hourBenefits: Medical benefits available at a costAbout The OpportunityWe are seeking an early-career Associate Scientist/Lab Technician II to support process engineering, continuous improvement, and laboratory activities within a sterile drug product manufacturing environment.This is a hands-on, process-focused position—not a traditional analytical chemistry role. Approximately 50% of the role will focus on process engineering and 50% on continuous improvement and laboratory support. You will help conduct laboratory studies, troubleshoot manufacturing challenges, evaluate process changes, and prepare technical reports summarizing experimental outcomes.Recent graduates with relevant laboratory experience are encouraged to apply. Previous pharmaceutical or manufacturing experience is preferred, but applicable internships, academic research, validation exposure, or technical operations experience will also be considered.What You’ll DoSupport laboratory studies involving sterile drug product processes, including formulation and filtration activities.Assist with process engineering and continuous improvement initiatives designed to improve quality, yield, throughput, cycle time, capacity, and cost.Investigate manufacturing and process-related challenges using structured problem-solving and scientific principles.Collect, analyze, and interpret process data to identify trends and improvement opportunities.Use statistical tools such as Minitab to support process monitoring and data analysis.Participate in change-request assessments and evaluate the potential impact of process, material, or technology changes.Write technical reports, scientific summaries, justification memos, protocols, and other documentation describing laboratory studies and experimental outcomes.Support process validation activities, including operational changes, new raw materials, and the introduction of new processes or technologies.Assist with experimental, demonstration, and validation lots.Maintain accurate and compliant laboratory and manufacturing documentation.Collaborate with Manufacturing, Quality, Engineering, Supply Chain, Operational Excellence, and EHS teams.Provide responsive laboratory and technical support for changing manufacturing priorities and time-sensitive activities.Follow applicable GMP, safety, environmental, and regulatory requirements.What We’re Looking ForAssociate, bachelor’s, or master’s degree in a scientific or engineering discipline.Degrees in Chemistry, Biology, Chemical Engineering, Biochemical Engineering, Bioengineering, Biomedical Engineering, or a related field are especially relevant.Previous hands-on laboratory experience through employment, internships, co-ops, or academic research.Interest in process engineering, pharmaceutical manufacturing, validation, technical operations, or continuous improvement.Ability to document experiments and communicate scientific findings through clear technical reports and memos.Strong organizational skills and the ability to adjust priorities in a dynamic, responsive environment.Effective written and verbal communication skills.Ability to work both independently and collaboratively after completing training.Preferred QualificationsExperience or internship exposure within pharmaceutical, biotechnology, medical device, or regulated manufacturing.Familiarity with sterile or aseptic manufacturing processes.Exposure to GMP requirements, process validation, technical operations, or manufacturing support.Experience with formulation, filtration, process troubleshooting, statistical process control, or Minitab.A combination of laboratory and manufacturing experience.Who Will Be Most Successful?This opportunity is ideal for a recent graduate or early-career scientific professional who enjoys solving process-related problems and wants to build experience within sterile pharmaceutical manufacturing. The successful candidate will be flexible, responsive, comfortable supporting last-minute laboratory activities, and capable of becoming increasingly independent after completing the initial training period.Candidates relocating to the area may be considered but must be able to relocate at their own expense.Interview ProcessThe interview process will include two virtual rounds, with a panel interview during the final stage.We are an equal opportunity employer and consider qualified applicants without regard to legally protected characteristics.People are our business worldwideOrion Group was founded in 1987 and is now one of the largest, independent, international recruitment companies. We have a network of 200 employees working from 24 offices, delivering a range of services – Talent Acquisition, Recruitment Outsourcing Services, Retained Search, Global Workforce Solutions, Completions & Commissioning and Materials Management – across 68 countries. As a global leader in workforce solutions, we recruit personnel across the Engineering & Technical, Office & Commercial, Scientific and Skilled Trades disciplines, for sectors including Oil & Gas, Life Science, Power & Utilities, Constructions & Infrastructure, Manufacturing and Renewables.Rachael Jalbuena Recruitment ConsultantShare thisApply for this roleFirst NameThis is a required fieldLast NameThis is a required fieldTelephone NumberThis is a required fieldEmail AddressThis is a required field A valid email address is required.CV, LinkedIn or Dropbox URLSelect upload option CV Upload LinkedIn / Dropbox URLThis is a required fieldCV UploadChoose FileThis is a required fieldLinkedIn / Dropbox URLThis is a required field A valid LinkedIn URL is required, please ensure it begins with https://www.linkedin.com/ A valid DropBox URL is required, please ensure it begins with https://www.dropbox.com/Do you have a right to work in the country this role is located in? Please Select -- Yes NoThis is a required fieldMessageBy submitting this form you agree to our Terms & Conditions, Privacy Policy & Cookie Policy This is a required fieldNot yet registered? Create an account todayAlready have an account? Sign in nowRecruitmentStill Looking? 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This is a 12-month PAYE contract commencing asap. What are we seeking: A background in Carbon Ca....View JobBack to resultsProcess Development Associate – Process Engineering & Sterile ManufacturingApply NowTR/083210 Posted: 24/07/2026$20 - $23 per hourUnited States, Illinois, North Chicago Contract Process Development Associate – Process Engineering & Sterile ManufacturingLocation: Hybrid – North Chicago/Lake County, IL 60064Contract: 1 year, with potential for extensionSchedule: Monday–Friday, standard business hoursPay: $20–$23/hourBenefits: Medical benefits available at a costWhat You’ll DoSupport laboratory studies involving sterile drug product processes, including formulation and filtration activities.Assist with process engineering and continuous improvement initiatives designed to improve quality, yield, throughput, cycle time, capacity, and cost.Investigate manufacturing and process-related challenges using structured problem-solving and scientific principles.Collect, analyze, and interpret process data to identify trends and improvement opportunities.Use statistical tools such as Minitab to support process monitoring and data analysis.Participate in change-request assessments and evaluate the potential impact of process, material, or technology changes.Write technical reports, scientific summaries, justification memos, protocols, and other documentation describing laboratory studies and experimental outcomes.Support process validation activities, including operational changes, new raw materials, and the introduction of new processes or technologies.Assist with experimental, demonstration, and validation lots.Maintain accurate and compliant laboratory and manufacturing documentation.Collaborate with Manufacturing, Quality, Engineering, Supply Chain, Operational Excellence, and EHS teams.Provide responsive laboratory and technical support for changing manufacturing priorities and time-sensitive activities.Follow applicable GMP, safety, environmental, and regulatory requirements.What We’re Looking ForAssociate, bachelor’s, or master’s degree in a scientific or engineering discipline.Degrees in Chemistry, Biology, Chemical Engineering, Biochemical Engineering, Bioengineering, Biomedical Engineering, or a related field are especially relevant.Previous hands-on laboratory experience through employment, internships, co-ops, or academic research.Interest in process engineering, pharmaceutical manufacturing, validation, technical operations, or continuous improvement.Ability to document experiments and communicate scientific findings through clear technical reports and memos.Strong organizational skills and the ability to adjust priorities in a dynamic, responsive environment.Effective written and verbal communication skills.Ability to work both independently and collaboratively after completing training.Preferred QualificationsExperience or internship exposure within pharmaceutical, biotechnology, medical device, or regulated manufacturing.Familiarity with sterile or aseptic manufacturing processes.Exposure to GMP requirements, process validation, technical operations, or manufacturing support.Experience with formulation, filtration, process troubleshooting, statistical process control, or Minitab.A combination of laboratory and manufacturing experience.Who Will Be Most Successful?This opportunity is ideal for a recent graduate or early-career scientific professional who enjoys solving process-related problems and wants to build experience within sterile pharmaceutical manufacturing. The successful candidate will be flexible, responsive, comfortable supporting last-minute laboratory activities, and capable of becoming increasingly independent after completing the initial training period.Candidates relocating to the area may be considered but must be able to relocate at their own expense.Interview ProcessThe interview process will include two virtual rounds, with a panel interview during the final stage.We are an equal opportunity employer and consider qualified applicants without regard to legally protected characteristics.People are our business worldwideOrion Group was founded in 1987 and is now one of the largest, independent, international recruitment companies. We have a network of 200 employees working from 24 offices, delivering a range of services – Talent Acquisition, Recruitment Outsourcing Services, Retained Search, Global Workforce Solutions, Completions & Commissioning and Materials Management – across 68 countries. As a global leader in workforce solutions, we recruit personnel across the Engineering & Technical, Office & Commercial, Scientific and Skilled Trades disciplines, for sectors including Oil & Gas, Life Science, Power & Utilities, Constructions & Infrastructure, Manufacturing and Renewables.Rachael Jalbuena Recruitment ConsultantShare thisApply for this roleFirst NameThis is a required fieldLast NameThis is a required fieldTelephone NumberThis is a required fieldEmail AddressThis is a required field A valid email address is required.CV, LinkedIn or Dropbox URLSelect upload option CV Upload LinkedIn / Dropbox URLThis is a required fieldCV UploadChoose FileThis is a required fieldLinkedIn / Dropbox URLThis is a required field A valid LinkedIn URL is required, please ensure it begins with https://www.linkedin.com/ A valid DropBox URL is required, please ensure it begins with https://www.dropbox.com/Do you have a right to work in the country this role is located in? Please Select -- Yes NoThis is a required fieldMessageBy submitting this form you agree to our Terms & Conditions, Privacy Policy & Cookie Policy This is a required fieldNot yet registered? Create an account todayAlready have an account? Sign in nowPosted 25/07/2026R&D Technician II (Biologics Sample Processing)TR/083214 $29 - $32 per hour United States, Massachusetts, Worcester Contract R&D Technician II (Biologics Sample Processing)Worcester, MALength of Contract: 6 monthsHourly Pay Rate: $29-32/hr (medical benefits available at a cost) Job Description Details:The Global Compoun....View JobPosted 25/07/2026Lab Tech III (Biologics Analytical Testing)TR/083213 $25 - $28 per hour United States, Illinois, North Chicago Contract Lab Tech III (Biologics Analytical Testing)Onsite in North Chicago, IL (1401 Sheridan Rd, North Chicago, IL 60064)1 Year Contract (Assignment is set to run for 12 months but could be extended base....View JobPosted 25/07/2026Senior Electrical, Instrumentation & Controls EngineerCR/083208 TBD based on experience and qualifications United States, West Virginia, Charleston Contract Join our client, a global EPCM, as a Senior Electrical, Instrumentation & Controls Engineer. In this EPC leadership role, you will lead complex industrial power distribution and power generation p....View JobPosted 24/07/2026Compensation Analyst / Total Rewards SpecialistTR/083211 $34 - $38 per hour United States, Illinois, Lake Bluff Contract Compensation Analyst / Total Rewards Specialist(HR Specialist III) Location: Lake County, IL (Hybrid) Schedule: Monday & Friday Remote | Tuesday–Thursday Onsite Duration: Initial 6-Month Contract ....View JobPosted 24/07/2026HSE Engineer - OperationsPR/083203 Competitive Scotland, Aberdeen City, Aberdeen Permanent Our client is currently recruiting for the position of HSE Engineer (Operations) based in Aberdeen. This is a permanent position offering hybrid working. They are looking for an experienced HSE En....View JobPosted 24/07/2026CCS Opportunity LeadTR/083202 PAYE Day Rate - Negotiable Scotland, Aberdeen City, Aberdeen Contract Our Operator client is currently recruiting for the position of Opportunity Lead based in Aberdeen. This is a 12-month PAYE contract commencing asap. What are we seeking: A background in Carbon Ca....View JobContact UsTelephone:+44 (0)1463-230860Find Us On Social:Quick Links Home About Us Resources Locations Job Search Policies & Associations Services Completions & Commissioning Global Workforce Solutions Materials Management Recruitment Outsourcing Services Retained Search Talent Acquisition Sectors Construction & Infrastructure Life Science Manufacturing Oil & Gas Power & Utilities Renewables 2026 © Copyright Orion Group. All rights reserved. All Policies Cookie Policy Privacy Statement Terms & Conditions HTML Sitemap Site by Venn