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Biotech Process Engineer Jobs (NOW HIRING)

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Process Engineer

Aiken, SC ยท On-site

$120K - $140K/yr

Process Engineer | $120K-$150K + Relocation + Stock Options Join an innovative biotech manufacturing company focused on sustainable bio-manufacturing in the Aiken/Augusta area! We are seeking a hands ...

Degree in Biochemical Engineering, Chemical Engineering, Biotechnology or related discipline with ... process development experience required. * Practical expertise with cGMP manufacturing and ...

Our hybrid biotechnology approaches unlock latent markets, providing access to sustainably produced ... Staff Process Engineer Summary The Staff Process Engineer, Downstream Processing (DSP) will take a ...

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... biotechnology & bio-engineering companies within the regulated industry for over 30 years. Since ... We are looking candidates with experience within regulated environment for a Process Engineer in ...

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... biotechnology & bio-engineering companies within the regulated industry for over 30 years. Since ... Experience supporting manufacturing or process engineering functions. * Excellent communication ...

... biotechnology today. Manus is seeking an experienced Process Engineer to serve as the technical ... subject matter expert (SME) for separations, liquid and dry powder handling, drying, and finished ...

... biotechnology today. Manus is seeking an experienced Process Engineer to serve as the technical ... subject matter expert (SME) for separations, liquid and dry powder handling, drying, and finished ...

Senior Process Engineer

Bend, OR ยท On-site

$109K - $141K/yr

... Biotechnology, Medical Device, and Life Sciences industries. I am actively connecting with ... Senior Process Engineer Location: Bend, OR Duration: 12+ Month Contract Position Overview We are ...

... biotechnology today. Manus is seeking an experienced Process Engineer to serve as the technical ... subject matter expert (SME) for separations, liquid and dry powder handling, drying, and finished ...

We are seeking an experienced Process Engineer to lead and support the successful transfer of ... pharmaceutical/biotech or medical device manufacturing environments Technical Experience:

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Biotech Process Engineer information

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$49.5K

$92K

$142.5K

How much do biotech process engineer jobs pay per year?

As of Aug 21, 2026, the average yearly pay for biotech process engineer in the United States is $92,018.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $103,000.00 per year, depending on experience, location, and employer.

What does a Biotech Process Engineer do?

A Biotech Process Engineer designs, develops, and optimizes processes used in the production of biological products such as pharmaceuticals, vaccines, and biofuels. They work closely with scientists and manufacturing teams to scale up lab procedures to industrial levels while ensuring product quality and regulatory compliance. Their role often involves troubleshooting equipment, improving efficiency, and implementing new technologies within biotech manufacturing environments.

What are the key skills and qualifications needed to thrive as a Biotech Process Engineer, and why are they important?

To thrive as a Biotech Process Engineer, you need a solid background in chemical or biochemical engineering, process design, and regulatory compliance, typically supported by a relevant bachelor's or master's degree. Familiarity with process control systems, bioprocess simulation software, and industry-standard quality systems such as cGMP is essential. Strong analytical thinking, problem-solving abilities, and effective teamwork and communication skills help you excel in cross-functional environments. These skills ensure efficient, compliant, and innovative bioprocess operations, which are critical for product quality and organizational success.

What are some common challenges faced by Biotech Process Engineers during scale-up from laboratory to production?

Biotech Process Engineers often encounter challenges when scaling up processes from laboratory or pilot scale to full production. These challenges can include maintaining product consistency, ensuring process sterility, and adapting equipment to handle larger volumes without compromising yield or quality. Engineers must also collaborate closely with cross-functional teams such as quality assurance, validation, and manufacturing to implement changes efficiently and adhere to regulatory standards. Proactive problem-solving and strong communication skills are key to overcoming these hurdles and ensuring successful technology transfer.

What is the difference between Biotech Process Engineer vs Biotech Manufacturing Technician?

AspectBiotech Process EngineerBiotech Manufacturing Technician
CredentialsBachelor's degree in biotech, chemical engineering, or related field; often requires experience in process designAssociate's or bachelor's degree; focus on operational skills and equipment handling
Work EnvironmentDesigning, optimizing, and overseeing production processes in labs or manufacturing facilitiesOperating and maintaining equipment on the manufacturing floor
Job FocusProcess development, scale-up, troubleshooting, and process improvementExecuting production tasks, quality checks, and equipment setup

Biotech Process Engineers focus on designing and improving manufacturing processes, requiring technical and analytical skills. In contrast, Biotech Manufacturing Technicians handle day-to-day production operations. Both roles are essential in biotech manufacturing but differ in responsibilities and required qualifications.

More about Biotech Process Engineer jobs

What cities are hiring for Biotech Process Engineer jobs?

Cities with the most Biotech Process Engineer job openings:

What states have the most Biotech Process Engineer jobs?

States with the most job openings for Biotech Process Engineer jobs include:

Infographic showing various Biotech Process Engineer job openings in the United States as of August 2026, with employment types broken down into 64% Full Time, and 36% Contract. Highlights an 93% In-person, and 7% Hybrid job distribution, with an average salary of $92,018 per year, or $44.2 per hour.

Senior Pharma / Biotech Process Engineer (Purification)

Visium Resources, Inc.

Kankakee, IL โ€ข On-site

$100K - $129K/yr

Contractor

Re-posted 9 days ago


Job description

Introduction
Visium Resources has been asked to identify qualified candidates for this Senior Pharmaceutical Process Engineer position with an emphasis onย Purification (Chrom, UFDF, Nanofiltration, TFF).ย 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 ย  ย  ย  ย  ย Feasibility
o ย  ย  ย  ย  ย Concept Design, Basic Design, Detailed Design
o ย  ย  ย  ย  ย Procurement
o ย  ย  ย  ย  ย Construction
o ย  ย  ย  ย  ย Project Monitoring/Governance
o ย  ย  ย  ย  ย 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.ย 
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