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Biotech Process Development Jobs in Illinois (NOW HIRING)

TekWissen LLC

Process Development Scientist

Rockford, IL · On-site

$30 - $35/hr

The job opportunity is for one of our clients specializing in biotechnology product development ... Process Development Scientist Location: Rockford, IL 61101 Duration: 12 Months Job Type: Temporary ...

Danaher

Senior Engineer, Process Validation

Chicago, IL · On-site +1

$100K - $130K/yr

... biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we ... At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking ...

Danaher

Senior Engineer, Process Validation

Chicago, IL · On-site +1

$100K - $130K/yr

... biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we ... At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking ...

IQVIA

CRA 1, IQVIA Biotech

Bloomington, IL

$71K - $145K/yr

... level financial processes or startup activities based on study needs. Accurate and timely ... We create intelligent connections to accelerate the development and commercialization of innovative ...

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Biotech Process Development information

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How much do biotech process development jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for biotech process development in Illinois is $30.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.73 and $33.80 per hour, depending on experience, location, and employer.

What is biotech process development?

Biotech process development refers to the design, optimization, and scale-up of manufacturing processes used to produce biological products, such as pharmaceuticals, enzymes, or vaccines. Professionals in this field work to turn laboratory procedures into efficient, large-scale industrial processes that meet regulatory and quality standards. This often involves selecting suitable equipment, optimizing conditions, ensuring reproducibility, and troubleshooting production issues. The ultimate goal is to produce high-quality products safely, consistently, and cost-effectively.

What is the difference between Biotech Process Development vs Biotech Manufacturing Associate?

AspectBiotech Process DevelopmentBiotech Manufacturing Associate
Primary FocusDesigning, optimizing, and scaling up bioprocesses for product developmentExecuting manufacturing processes to produce biopharmaceuticals at scale
Work EnvironmentLaboratories and pilot plant facilitiesProduction floors and manufacturing plants
Required SkillsProcess design, lab techniques, troubleshootingEquipment operation, quality control, adherence to SOPs
Typical CredentialsBSc/MSc in Biotechnology, Chemical Engineering, or related fieldsBSc in Biotechnology, Biology, or related fields

While both roles are essential in biotech, Biotech Process Development focuses on creating and optimizing processes during product development, whereas Biotech Manufacturing Associates handle the day-to-day production to ensure consistent product quality at scale.

What are the key skills and qualifications needed to thrive in Biotech Process Development, and why are they important?

To excel in Biotech Process Development, you need a strong background in bioprocess engineering, molecular biology, and chemistry, typically supported by a degree in biotechnology or related fields. Familiarity with tools such as bioreactors, chromatography systems, and data analysis software, along with certifications in Good Manufacturing Practice (GMP), is highly valuable. Strong problem-solving skills, attention to detail, and effective teamwork distinguish top performers in this role. These competencies are crucial for optimizing processes, ensuring product quality, and driving innovation in the biotech industry.

What are some common challenges faced by professionals in Biotech Process Development, and how are they typically addressed?

Professionals in Biotech Process Development often encounter challenges related to scaling up processes from the laboratory to commercial production, ensuring product consistency, and meeting strict regulatory standards. Addressing these challenges typically involves close collaboration with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing. Continuous process optimization, thorough documentation, and robust validation protocols are essential strategies to overcome these hurdles and ensure successful product development and commercialization.
What are popular job titles related to Biotech Process Development jobs in Illinois? For Biotech Process Development jobs in Illinois, the most frequently searched job titles are:
What job categories do people searching Biotech Process Development jobs in Illinois look for? The top searched job categories for Biotech Process Development jobs in Illinois are:
What cities in Illinois are hiring for Biotech Process Development jobs? Cities in Illinois with the most Biotech Process Development job openings:
Biotech Process Development jobs near you
Senior Pharma / Biotech Process Engineer (Purification)

Senior Pharma / Biotech Process Engineer (Purification)

Visium Resources, Inc.

Kankakee, IL • On-site

$100K - $129K/yr

Contractor

Posted 14 days ago

Job description

Introduction
Visium Resources has been asked to identify qualified candidates for this Senior Pharmaceutical Process Engineer position with an emphasis on Purification (Chrom, UFDF, Nanofiltration, TFF). This position is a direct hire opportunity which is expected to be on-site in Kankakee, Illinois.


Summary

Client is seeking an experienced Senior Process Engineer to support a major pharmaceutical capital expansion project at manufacturing campus in Kankakee, Illinois.


Client is seeking an experienced Senior Process Engineer - Purification to support a major pharmaceutical capital expansion project at manufacturing campus in Kankakee, Illinois.

Serving as the Owner's Representative, this individual will provide technical leadership throughout the design, procurement, fabrication, installation, commissioning, qualification, and startup of downstream purification systems. The successful candidate will ensure that engineering deliverables prepared by the Architect/Engineer (A/E), equipment manufacturers, and system suppliers meet the Owner's User Requirements Specifications (URS), process performance requirements, GMP standards, and long-term operational objectives.

The Senior Process Engineer will work closely with Process Engineering, Automation, Commissioning & Qualification (C&Q), Validation, Manufacturing, Quality, Construction, Procurement, and equipment vendors to successfully deliver complex purification systems supporting plasma-derived therapeutics and biologics manufacturing.


Job Description:

Provide technical guidance into the design, project management, commissioning and start-up of equipment and facilities, for upgrades, renovations and expansions of client facilities and processes.
Support project execution from Feasibility through to project completion/handover, including all project stages such as:
o          Feasibility
o          Concept Design, Basic Design, Detailed Design
o          Procurement
o          Construction
o          Project Monitoring/Governance
o          Commissioning & Qualification

Prepare/perform/review process engineering drawings, calculations, whether as part of engineering design or as part of verification of calculations of vendors/client/other consultants, or Junior Engineers. Drawings may include PFDs, P&IDs as well as others. Calculations may include heat exchanger, pump, piping, control valve sizing, heat and mass balances, as well as other engineered calculations. 
Prepare/review technical specifications and data sheets for various equipment, instrumentation, and systems (such as vessel data sheets, etc).
Review technical documentation such as SDS/HDS, layouts, manuals, datasheets.
Manage other engineering design firms, equipment vendors, construction firms, and internal/external stakeholders as required to execute projects.
Integrate safety into the design and execution of all projects (HAZOP reviews, PHSRs, design reviews with EHS representatives).
Prepare/review User Requirements Specifications (URS)
Provide input into Commissioning (FAT, SAT) and Qualification Protocols (IQOQ), as well as support execution of Commissioning & Qualification.
Prepare/review automation sequences, as required for Process Automation, such as Functional Specifications, Valve & Alarm Matrices.
Coordination with other engineering disciplines and other cross-functional departments (automation engineering, facilities engineering, process engineering, validation, project management, operations, quality, safety).
Facilitate project management tools throughout the execution of projects, such as procurement tracking, vendor management, meeting minutes / action lists, risk register log, schedule updates, project updates.
Coordinate meetings with cross-functional departments, to drive project progress, facilitate decisions, provide updates.
Travel may be occasionally required for meetings with the client and equipment fabrication vendors or Factory Acceptance Testing (FATs).
Work may require occasional support over shutdowns or extended hours, specifically during installation and commissioning / validation phases.
Client-management (maintain key Client relationships in support of business development and pursuit of new work), project scheduling/budgeting, coordination of client and company resources for effective project delivery, supporting business development (providing technical support to the sales as required for proposals/opportunities), presenting at industry conferences/publishing papers etc.
Visit construction and installation sites.
Supervise contractors during critical installations of process equipment and associated utilities.
Other duties as assigned by client, and/or the company, based on workload and project requirements.



Qualified candidates would have the following:

Knowledge of GMP requirements for working in pharma/biotech facilities, with a Basic understanding of SOPs, Validation, Change Controls.
10+ years of experience pharma process engineering experience, with at least 6 years of bioprocess engineering experience (upstream or downstream)
Excellent written and spoken English is required including the preparation of technical documents in English
Experience in leading teams.
Experience with, and knowledge of some of the typical Biotechnology processes & peripheral systems is required; Upstream Biotech Processes (Fermentation, Bioreactors, Centrifugation, Thawing), Downstream / Purification Biotech Processes (chromatography, TFF, DF, NF-MF), Fill & Finish equipment, Media Preparation, CIP/SIP systems, Buffer Preparation, clean utilities (PW, WFI, CS, PS)
Possess leadership skills, and be able to take initiative to lead projects, involving multiple stakeholders, departments, and varying complexity.
Possess mentorship skills, to coach and develop junior and intermediate employees.
Basic knowledge of AutoCAD is an asset.
Engineering degree, preferably in Chemical, Biochemical, Mechanical Engineering or a related discipline.

Purification Process Experience
Candidates should possess significant experience with several of the following downstream processing technologies:
  • Chromatography Systems
  • Ultrafiltration/Diafiltration (UF/DF)
  • Tangential Flow Filtration (TFF)
  • Nanofiltration Systems
  • Virus Filtration
  • Process Buffer Preparation and Distribution
  • Process Holding Vessels
  • Single-Use Flow Paths and Assemblies
  • CIP/SIP Systems
  • Bioprocess Skid Packages

________________________________________________________________________________________________


Visium Resources is an award-winning employment firm with a mission to match talented individuals with highly successful organizations. At Visium, our company"s success is based on your success. When you work with us, you are never 'just a number'. You are our most important asset. Here, you will know us by name through our regular visits to client sites and even occasional luncheons. We will always be there when you need assistance and will always go the extra mile to ensure that you are as successful as possible. Whether you're looking for contract, contract-to-hire or permanent opportunities, we firmly believe there is no employment agency that will work harder for you than Visium.
Visium Resources is an equal opportunity employer and values diversity. All employment is decided based on qualifications, merit and business need.

Education:BS/BA DegreeEmployment Type: CONTRACTOR

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