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Biotech Manufacturing Jobs in Minnesota (NOW HIRING)

Danaher

Staff Manufacturing Scientist

Chaska, MN · On-site

... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... The Staff Manufacturing Scientist is responsible for responsible for leading and supporting complex ...

Danaher

Staff Manufacturing Scientist

Chaska, MN · On-site

... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... The Staff Manufacturing Scientist is responsible for responsible for leading and supporting complex ...

Microbiologics, Inc.

R&D Scientist

Saint Cloud, MN · On-site

$86K - $107K/yr

... biotechnology company and trusted partner to healthcare and life science organizations worldwide. For more than 50 years, we have supported laboratories, manufacturers, and suppliers with high ...

Microbiologics

R&D Scientist

Saint Cloud, MN

... biotechnology company and trusted partner to healthcare and life science organizations worldwide. For more than 50 years, we have supported laboratories, manufacturers, and suppliers with high ...

BioMADE

Shift Supervisor

Maple Grove, MN · On-site

$95K - $115K/yr

Operating as a contract development and manufacturing organization (CDMO), this pilot plant will help bridge a gap in the domestic biotech industry (non-pharma), providing clients with emerging ...

TekWissen LLC

Buyer II

Bloomington, MN · On-site

$30 - $31/hr

This client is a German multinational Pharmaceutical and biotechnology company and one of the ... Coordinates purchasing activities with manufacturing, facility, and engineering departments to ...

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All JobsBiotech Manufacturing JobsBiotech Manufacturing Jobs in Minnesota

Biotech Manufacturing information

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$32

How much do biotech manufacturing jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for biotech manufacturing in Minnesota is $20.41, according to ZipRecruiter salary data. Most workers in this role earn between $16.01 and $22.84 per hour, depending on experience, location, and employer.

What is biotech manufacturing?

Biotech manufacturing is the process of producing products using biological systems or living organisms, such as bacteria, yeast, or mammalian cells. This field is crucial for making pharmaceuticals, vaccines, enzymes, and other biological products on a large scale. Biotech manufacturing involves a combination of biology, chemistry, and engineering to ensure products are made efficiently, safely, and to high quality standards. It is a key part of the biotechnology industry and is vital for developing new medical treatments and therapies.

What are the key skills and qualifications needed to thrive in biotech manufacturing?

To excel in Biotech Manufacturing, a background in biology, chemistry, or engineering with knowledge of GMP (Good Manufacturing Practices) is typically required. Familiarity with bioprocessing equipment, laboratory information management systems (LIMS), and relevant certifications such as Six Sigma or ASQ is often expected. Attention to detail, problem-solving abilities, and strong teamwork skills help professionals stand out in this environment. These competencies are crucial for ensuring safe, efficient, and compliant production of biotechnological products.

What are some common challenges faced in biotech manufacturing, and how can new team members prepare for them?

In biotech manufacturing, common challenges include maintaining strict quality standards, adhering to complex regulatory requirements, and troubleshooting equipment or process issues. New team members can prepare by familiarizing themselves with Good Manufacturing Practices (GMP), developing strong attention to detail, and being proactive in learning about the latest industry protocols. Teamwork is essential, as much of the work involves cross-functional collaboration with quality assurance, engineering, and research departments to ensure smooth production and compliance.

What is the difference between Biotech Manufacturing vs Biotech Quality Control?

AspectBiotech ManufacturingBiotech Quality Control
CredentialsTypically requires a degree in biotech, biology, or chemistrySimilar credentials, often with additional certifications in quality assurance
Work EnvironmentProduction floors, laboratories, cleanroomsLaboratories, testing facilities, quality assurance labs
Employer & Industry UsageManufacturing plants, biotech companies, pharmaceutical firmsQuality assurance departments within biotech and pharma companies
Common Search & ComparisonBiotech Manufacturing vs Biotech Quality Control

Biotech Manufacturing focuses on producing biotech products, involving process development and production. Biotech Quality Control emphasizes testing and ensuring product quality, often working closely with manufacturing but with a focus on compliance and standards.

What are popular job titles related to Biotech Manufacturing jobs in Minnesota?

For Biotech Manufacturing jobs in Minnesota, the most frequently searched job titles are:

What job categories do people searching Biotech Manufacturing jobs in Minnesota look for?

The top searched job categories for Biotech Manufacturing jobs in Minnesota are:

Biotech Manufacturing jobs near you
Infographic showing various Biotech Manufacturing job openings in Minnesota as of August 2026, with employment types broken down into 89% Full Time, 3% Part Time, 6% Contract, and 2% Nights. Highlights an 94% Physical, 3% Hybrid, and 3% Remote job distribution, with an average salary of $42,449 per year, or $20.4 per hour.

Sr Process Engineer

Takeda Pharmaceutical Company Limited

Brooklyn Park, MN • On-site

$108K - $140K/yr

Full-time

Re-posted 8 days ago

Takeda Pharmaceuticals rating

7.3

Company rating: 7.3 out of 10

Based on 71 frontline employees who took The Breakroom Quiz

70th of 86 rated pharmaceutical

Job description

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description
About the Role:

Serve as the Engineering subject matter expert for a specific process area (cell culture, harvest, purification, clean-in-place, or utilities systems)

Ensure systems remain in a qualified state. Act as technical owner for system lifecycle including design, installation, qualification, production support, deviation resolution, maintenance, and decommissioning

Monitor system reliability and performance. Develop and implement engineering solutions to complex problems. Lead programs related to system qualification, asset management, project execution, and Good Engineering Practices. Support development of site staff on technical and procedural topics

How you will contribute:
  • Develop engineering deliverables including Process Flow Diagrams, P&IDs, System Specifications, and Functional Specifications
  • Implement system modifications under cGMP change control
  • Develop and execute FAT, commissioning protocols, and qualification protocols
  • Develop calibration and preventative maintenance plans
  • Lead deviation investigations and implement corrective and preventative actions
  • Participate in capital planning, spending, and tracking
  • Serve as project manager on small to medium projects under $5M
  • Interface with cross-functional teams to meet project goals
  • Stay current with industry best practices and technologies
  • Complete required training within timeframe
  • Selecting technologies, designing equipment, and diagnosing process issues
  • Making data-driven decisions using engineering principles
  • Ensuring impact to product quality, safety, reliability, and throughput
  • Maintaining regulatory compliance and validation requirements
  • Troubleshooting factory floor issues and supporting capacity planning
  • Managing impact to uptime, batch continuity, and manufacturing schedule
  • Responding to urgency and severity of equipment failures
  • Determining escalation thresholds
  • Balancing short-term mitigation versus long-term solutions
  • Perform other duties as assigned
What you bring to Takeda:
  • Bachelor's degree in Engineering
  • 3 or more years of relevant experience
  • Experience in pharmaceutical or biotechnology manufacturing environment
  • Engineer-in-Training (EIT) or Professional Engineer license preferred
  • Demonstrated track record supporting process operations and projects in an FDA-regulated environment
  • Knowledge of engineering principles including fluid mechanics, heat transfer, thermodynamics, and mass transfer
  • Experience applying project management methodologies
  • Understanding of commissioning and qualification protocol development
  • Direct experience with systems such as bioreactors, centrifugation, chromatography, tangential flow filtration, CIP, autoclaves, clean utilities, and HVAC
  • Familiarity with instrumentation and sensing technologies in pharmaceutical manufacturing
  • Experience with regulatory requirements and GMP environments
  • Experience supporting large capital projects
  • Familiarity with batch control systems, data historians, SQL, and scripting (preferred)
  • Knowledge of automation, PLCs, power systems, and controls (desirable)
  • Proficient in MS Office (Word, Excel, PowerPoint) and MS Project
  • Ability to work in fast-paced, cross-functional teams
  • Strong planning, prioritization, and escalation judgment
Important Considerations

At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product. In this role, you may:

  • Combination of sedentary work and facility walkdowns
  • Occasional ladder climbing
  • Ability to lift up to 25 lbs
  • Participation in 24/7 on-call rotation
  • Use of PPE and clean room garments as required
  • Infrequent travel up to approximately 25% during project activities
More about us:

At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.

Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

#GMSGQ #ZR1 #LI-Onsite

Takeda Compensation and Benefits Summary

We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.

For Location:

Brooklyn Park, MN

U.S. Base Salary Range:

$89,900.00 - $141,240.00


The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.


For information about our benefits, please click here.


EEO Statement

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.

LocationsBrooklyn Park, MNWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull time

Job Exempt

Yes

What Takeda Pharmaceuticals employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Takeda Ventures logo

About Takeda Ventures

Sourced by ZipRecruiter

Industry

Investment clubs and venture capital companies, pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

1 - 10 Employees

Headquarters location

San Diego, CA, US

Social media

Twitter

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