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Biotech Manufacturing Associate (277467)

Vacaville, CA · On-site

$25/hr

Biotech Manufacturing Associate Location: Vacaville , CA 95688 (Onsite) Duration: 12+ Months Rate details: Day shift (Shift 1): $25.00/hr, Night shift (Shift 3): $27.50/hr Note: (These roles follow a ...

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System One Holdings, LLC

Manufacturing Associate

Novato, CA · On-site

$28 - $32.20/hr

Thursday - Saturday with Alternating Wednesdays (6am to 7pm) / Rotating 12hour shift Overview Leading biotechnology company looking for an experienced Manufacturing Associate. Ideal candidates should ...

System One Holdings, LLC

Manufacturing Associate

Novato, CA · On-site

$28 - $32.20/hr

Alternating Saturdays /Sundays to Tuesdays from 6pm to 7 am Overview Leading biotechnology company looking for an experienced Manufacturing Associate. Ideal candidates should have a Bachelor's degree ...

System One Holdings, LLC

Manufacturing Associate

Novato, CA · On-site

$28 - $32.20/hr

Sunday - Tuesday 6:00 p.m. - 7:00 a.m., with alternating Saturdays Overview Leading biotechnology company looking for an experienced Manufacturing Associate. Ideal candidates should have a Bachelor ...

Integrated Resources INC

Manufacturing Engineer

Raleigh, NC

$71K - $91K/yr

Experience Requirements: 2 - 3 years' experience in pharmaceutical or biotech manufacturing environment Skills and Qualifications: Practical knowledge and application of GMP and EMEA regulations. Two ...

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How much do biotech manufacturing jobs pay per hour?

As of Jun 8, 2026, the average hourly pay for biotech manufacturing in the United States is $20.84, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $23.32 per hour, depending on experience, location, and employer.

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

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 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.
More about Biotech Manufacturing jobs
What cities are hiring for Biotech Manufacturing jobs? Cities with the most Biotech Manufacturing job openings:
What are the most commonly searched types of Biotech Manufacturing jobs? The most popular types of Biotech Manufacturing jobs are:
What states have the most Biotech Manufacturing jobs? States with the most job openings for Biotech Manufacturing jobs include:
What job categories do people searching Biotech Manufacturing jobs look for? The top searched job categories for Biotech Manufacturing jobs are:
Biotech Manufacturing jobs near you
Infographic showing various Biotech Manufacturing job openings in the United States as of May 2026, with employment types broken down into 69% Full Time, 2% Part Time, 4% Temporary, and 25% Contract. Highlights an 98% In-person, and 2% Hybrid job distribution, with an average salary of $43,341 per year, or $20.8 per hour.
Engineer, Biotech Manufacturing Line (JP12155)

Engineer, Biotech Manufacturing Line (JP12155)

3 Key Consulting

New Albany, OH

$35 - $37/hr

Other

Posted 9 days ago

Job description

Job Title: Engineer, Biotech Manufacturing Line (JP12155)
Location: New Albany, OH. 43054
Business Unit: Assembly & Packaging
Employment Type: Contract
Duration: 1+ years (with possible extensions)
Rate: $35 - $37/hour
Posting Date: 1/10/2024.
Notes: Only qualified candidates need apply. Fully onsite in New Albany OH. 43054
3 Key Consulting is hiring! We are recruiting an Engineer Biotech Manufacturing Line for a consulting engagement with our direct client, a leading global biotechnology company.
Job Description:
In this role the Line Owner/System Owner must work under general supervision, owning all the technical aspects in a manufacturing line. The processes where the SO/LO Engineer shall be familiar with are:
  • Characterization of process optimization strategies and/or solving problems of operational issues in the packaging operations, manufacturing, pilot technologies or capital projects.
  • Applies basic engineering principles to the design and implementation of system modifications, experiments and/or capital projects.
  • Organizes, analyzes and presents interpretation of results for operational issues or engineering projects of minor scope and complexity.

As a technical resource of an area, System owner / Line Owner Engineer shall interact and provide direction to technical resources such as Mechanics, Automation Techs and IS teams. At the same time, the System Owner/Line Owner Engineer shall be able to define designs requirement to the service providers to fulfill area technical and equipment needs.
Top Must Have Skill Sets:
  • Experience with packaging equipment, specifically pharmaceutical, food, or beverage.
  • Experience with GMP environments.
  • Good communication skills, troubleshooting skills, and a team player.
  • Looking for Mechanical engineer over an industrial engineer (industrial is OK with relevant experience)

Day to Day Responsibilities:
Specific responsibilities include but are not limited to:
  • Provide solutions to a variety of technical problems of moderate scope and complexity.
  • Under general supervision will evaluate, select and apply standard engineering techniques and procedures. Assistance given for unusual problems.
  • Perform assignments that have clear and specific objectives and require investigation of limited number of variables.
  • Initiate and complete routine technical tasks.

Operations Engineering:
  • Function as a technical specialist to equipment or systems regarding problem solving operations. Frequently become actively involved in daily operations when required to meet schedules or to resolve problems.
  • Routinely audit the operational performance and regulatory compliance of a moderate number of equipment items or systems of complexity.
  • Work with research, manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation departments in developing requirements and recommendations for system modifications.

Design Engineering:
  • Work under the direct supervision of project managers to complete design, engineering, and construction projects within schedule and budget constraints.
  • Work with consultants, architects and engineering firms on development of standard design documents.
  • Acquire and critique quotes for equipment modifications or installations.
  • Generate rudimentary project cost estimates and schedules.

Basic Qualifications:
Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience
Preferred Qualifications:
  • Advanced degree in Mechatronics, Computer, Electrical, Mechanical, or Chemical Engineering
  • Knowledge and/or experience of pharmaceutical/biotech processes, especially in the area of final drug product operations
  • Knowledge of pharmaceutical/biotech processes
  • Familiarity with validation processes for Packaging areas
  • Familiarity with serialization process and networking
  • Familiarity with documentation in a highly regulated environment
  • Ability to operate specialized equipment, tools and computers as appropriate.
  • Ability to interpret and apply GAMPs and GMPs and familiarity with documentation in a highly regulated environment.
  • Ability to apply engineering science to production.
  • Able to develop solutions to routine technical problems of limited scope
  • Comprehensive understanding of protocol requirements.
  • Organizational, project management, problem-solving, as well as validation protocol, and technical writing capability
  • Excellent communication (verbal/written) and presentation skills
  • Demonstrated interpersonal skills including; collaboration, influencing, and facilitation
  • Protocol and script testing Writing
  • Dealing with and handling change
  • Packaging Equipment Technical knowledge
  • Analytical Problem Solving
  • Comprehensive understanding of validation protocol implementation requirements as well as knowledge of validation processes and requirements as applied to new equipment installations
  • Understanding of Operational Excellence and Lean Transformation in the Automation and Engineering Context

Why is the Position Open?
Supplement additional workload on team.
Red Flags:
Misspellings in Resume.
Long Resumes without descriptive content.
Interview Process:
One phone and one virtual panel interview.
We invite qualified candidates to sendyour resume toresumes@3keyconsulting.com. Ifyou decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our websitewww.3keyconsulting.com/careers. You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.

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