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Biotech Manufacturing Associate Jobs in Iowa (NOW HIRING)

Actalent

Research Associate

Des Moines, IA

$23/hr

... Food Science, Biotechnology, or a closely related field. * Previous hands-on microbiology ... Comfort working in a bio/chemical manufacturing facility and following Good Manufacturing Practices ...

Iff

QA Lab Analyst

Cedar Rapids, IA

Associate's or Bachelor's degree in Microbiology, Biochemistry, Chemistry, or a related field * 1-3 ... Experience working in QA/QC within a biotechnology or manufacturing environment * Familiarity with ...

Kemin

Sr. CLS Associate

Des Moines, IA · On-site

We are a privately held, family-owned-and-operated global biotechnology company driven by curiosity ... We employ 3,500 global employees and operations in 90 countries, including manufacturing facilities ...

TekWissen LLC

CAD Technician

Muscatine, IA · On-site

This client is a German multinational Pharmaceutical and biotechnology company and one of the ... Associate degree in Drafting/Design Technology or equivalent. Competencies/Skills: The position ...

Iff

Production Technician

Cedar Rapids, IA

$27/hr

Associate or Bachelor's degree in a technical or scientific field preferred * 2+ years of ... Experience in biotechnology, chemical, or food manufacturing environments * Familiarity with Delta ...

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Biotech Manufacturing Associate information

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$11

$19

$31

How much do biotech manufacturing associate jobs pay per hour?

As of Aug 4, 2026, the average hourly pay for biotech manufacturing associate in Iowa is $19.57, according to ZipRecruiter salary data. Most workers in this role earn between $15.34 and $21.92 per hour, depending on experience, location, and employer.

What is a biotech manufacturing associate?

Biotech Manufacturing Associates are professionals who work in the production of biotechnology products, such as pharmaceuticals, vaccines, and other biologically derived materials. They are responsible for operating equipment, following strict protocols, and maintaining sterile environments to ensure product quality and safety. Their duties often include preparing materials, monitoring production processes, troubleshooting equipment issues, and documenting all activities according to regulatory standards. This role is essential in ensuring that biotech products are manufactured efficiently and meet both industry and government regulations.

What does a biotech manufacturing associate do?

A biotech manufacturing associate is responsible for producing biological products in a laboratory or manufacturing setting, following strict safety and quality protocols. They operate equipment, prepare materials, monitor processes, and document production activities to ensure compliance with regulatory standards. Strong attention to detail and knowledge of GMP (Good Manufacturing Practice) are essential for this role.

What is the difference between Biotech Manufacturing Associate vs Laboratory Technician?

AspectBiotech Manufacturing AssociateLaboratory Technician
CredentialsHigh school diploma or equivalent; some roles may require associate degreeHigh school diploma or equivalent; some roles may require associate degree or certification
Work EnvironmentManufacturing floor, production lines, cleanroomsLaboratories, research facilities, testing environments
Industry UsageBiotech manufacturing, pharmaceutical productionResearch labs, quality control, testing labs

While both roles support biotech operations, a Biotech Manufacturing Associate primarily works on production and manufacturing processes in a cleanroom environment, focusing on assembling, monitoring, and maintaining manufacturing equipment. In contrast, a Laboratory Technician typically conducts experiments, tests, and quality control procedures in a laboratory setting. Both roles require attention to detail and adherence to safety protocols, but their daily tasks and work environments differ significantly.

What are some common challenges faced by biotech manufacturing associates, and how can they be managed effectively?

Biotech Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), troubleshooting equipment malfunctions, and working under tight production deadlines. Effective management of these challenges involves strong attention to detail, proactive communication with cross-functional teams such as quality assurance and engineering, and continuous learning to stay updated on new protocols and technologies. Developing problem-solving skills and embracing a collaborative mindset can also help associates consistently contribute to high-quality production outcomes.

What are the key skills and qualifications needed to thrive as a biotech manufacturing associate?

To thrive as a Biotech Manufacturing Associate, you typically need a background in biology, chemistry, or a related field, along with experience in GMP-regulated environments. Familiarity with bioprocessing equipment, laboratory instrumentation, and documentation systems such as batch records is crucial. Attention to detail, teamwork, and strong problem-solving abilities help you excel in this collaborative and regulated field. These skills ensure the consistent production of safe, high-quality biotech products while maintaining compliance with industry standards.
What are popular job titles related to Biotech Manufacturing Associate jobs in Iowa? For Biotech Manufacturing Associate jobs in Iowa, the most frequently searched job titles are:
What job categories do people searching Biotech Manufacturing Associate jobs in Iowa look for? The top searched job categories for Biotech Manufacturing Associate jobs in Iowa are:
What cities in Iowa are hiring for Biotech Manufacturing Associate jobs? Cities in Iowa with the most Biotech Manufacturing Associate job openings:
Biotech Manufacturing Associate jobs near you
Infographic showing various Biotech Manufacturing Associate job openings in Iowa as of July 2026, with employment types broken down into 1% As Needed, 70% Full Time, 27% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $40,709 per year, or $19.6 per hour.

Senior Associate - Manufacturing Engineering

Elanco Animal Health Incorporated

Fort Dodge, IA • On-site

$101K - $138K/yr

Full-time

Posted 14 days ago

Elanco rating

7.8

Company rating: 7.8 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

52nd of 86 rated pharmaceutical

Job description

At Elanco (NYSE: ELAN) - it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose - all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals' lives better makes life better - join our team today!
Your Role: Lead Commissioning, Qualification & Validation (CQV) Engineer
As the Lead CQV Engineer, you will be part of the Engineering team responsible for leading the Commissioning, Qualification, and Validation (CQV) program for the Fort Dodge manufacturing site. In this role, you will provide technical leadership to ensure manufacturing equipment and systems are commissioned, qualified, and validated in compliance with GMP requirements while driving continuous improvement, standardization, and operational excellence across the site.
Your Responsibilities
  • Lead the site-wide Commissioning, Qualification, and Validation (CQV) program, ensuring compliance with Elanco standards and regulatory requirements.
  • Develop, maintain, and improve CQV business processes, including ownership of SOPs, templates, and qualification documentation.
  • Provide technical guidance and oversight for equipment commissioning, qualification, validation, and engineering projects while managing internal and external CQV resources.
  • Drive continuous improvement through Lean principles, process optimization, and collaboration with Engineering, Quality Assurance, and cross-functional teams.
  • Champion a strong safety culture by evaluating equipment and systems for potential safety risks and ensuring safe, compliant operations.

What You Need to Succeed (minimum qualifications)
  • Education: Bachelor's degree in engineering.
  • Experience: Minimum of 3 years of Commissioning, Qualification, and Validation (CQV) experience within the life sciences, pharmaceutical, biotechnology, or manufacturing industry.
  • Top 2 skills: Strong knowledge of GMP regulations, equipment commissioning, qualification and validation, combined with proven leadership and project management abilities.

What Will Give You a Competitive Edge (preferred qualifications)
  • Experience leading CQV programs for pharmaceutical, biologics, or vaccine manufacturing facilities.
  • Demonstrated success managing external contractors and cross-functional project teams.
  • Experience implementing Lean manufacturing and continuous improvement initiatives.
  • Strong understanding of regulatory compliance, risk management, and validation lifecycle principles.
  • Excellent communication skills with the ability to influence technical and non-technical stakeholders while driving project execution.

Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job-related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.

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