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Fda Contract Jobs in Iowa (NOW HIRING)

Cambrex

Automation Engineer

Charles City, IA · On-site

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... All employees are required to adhere to DEA, EPA, FDA and cGMP regulations as they relate to the ...

Cambrex

Automation Engineer

Charles City, IA

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... All employees are required to adhere to DEA, EPA, FDA and cGMP regulations as they relate to the ...

Cambrex

Automation Technician

Charles City, IA · On-site

$38K/yr

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... All employees are required to adhere to DEA, EPA, FDA and cGMP regulations as they relate to the ...

Cambrex

Lab Support Technician

Charles City, IA

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... All employees are required to adhere to EPA, DEA, FDA and cGMP regulations as they relate to the ...

Cambrex

QA Data Coordinator

Charles City, IA · On-site

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... cGMP, FDA, DEA, and EPA requirements. The role ensures production documentation is accurate ...

Cambrex

Senior Project Manager

Charles City, IA

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... FDA and cGMP regulations as they relate to the operation of the Company; and to adhere to all ...

Cambrex

Pharma Operator

Charles City, IA

$16 - $21.50/hr

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... Adhere to all EPA, FDA and cGMP regulations as they relate to the operation of the chemical ...

Cambrex

Pharma 3/4 Operator

Charles City, IA · On-site

$16 - $21.50/hr

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... Adhere to all EPA, FDA and cGMP regulations as they relate to the operation of the chemical ...

Cambrex

Chem 2 Operator

Charles City, IA

$16 - $19.75/hr

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... Adhere to all EPA, FDA and cGMP regulations as they relate to the operation of the chemical ...

Cambrex

Senior Operator

Charles City, IA

$16 - $21.50/hr

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... Perform the job duties of an Operator All coworkers are required to adhere to DEA, EPA, FDA and ...

Varsity Tutors

Biomedical Engineering Tutor

Ames, IA · Remote

$18 - $40/hr

... FDA regulatory requirements. Adapts instruction using case studies of medical devices, MATLAB ... Varsity Tutors does not contract in: Alaska, California, Colorado, Delaware, Hawaii, Maine, New ...

Varsity Tutors

Biomedical Engineering Tutor

Iowa City, IA · Remote

$18 - $40/hr

... FDA regulatory requirements. Adapts instruction using case studies of medical devices, MATLAB ... Varsity Tutors does not contract in: Alaska, California, Colorado, Delaware, Hawaii, Maine, New ...

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Fda Contract information

See Iowa salary details

$38.5K

$99.6K

$130.6K

How much do fda contract jobs pay per year?

As of Aug 26, 2026, the average yearly pay for fda contract in Iowa is $99,594.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,600.00 and $111,800.00 per year, depending on experience, location, and employer.

What is an Fda contract?

An FDA Contract job refers to a temporary or project-based position working with or for the U.S. Food and Drug Administration (FDA) through a contractual agreement. These roles can be with the FDA directly or through third-party contractors supporting FDA initiatives. Responsibilities may include regulatory compliance, data analysis, scientific research, IT support, or administrative tasks. Contract positions vary in duration and benefits but provide opportunities to work in a highly regulated environment.

What are the primary responsibilities of someone working under an Fda contract?

As an FDA Contract professional, your primary responsibilities usually include developing, reviewing, and managing documents and agreements in accordance with FDA guidelines and regulations. You may coordinate closely with regulatory affairs, legal, and project management teams to ensure that all contract terms support compliance and meet project timelines. Daily tasks might involve drafting and negotiating contract language, tracking deliverables, and supporting regulatory submissions. This role is both detail-oriented and collaborative, and it provides valuable experience for those seeking advancement into regulatory management or specialist positions.

What are the key skills and qualifications needed to thrive in the Fda contract position, and why are they important?

To thrive in an FDA Contract role, you need strong knowledge of FDA regulations, compliance processes, and contract management, often supported by a background in life sciences or regulatory affairs. Familiarity with tools such as Document Control Systems, eCTD publishing software, and experience with regulatory submission platforms are typically required. Outstanding attention to detail, negotiation skills, and the ability to collaborate across cross-functional teams help candidates excel. These competencies are critical for ensuring contracts meet strict regulatory standards and for navigating the complexities of FDA approval and compliance procedures.

What are the most commonly searched types of Fda jobs in Iowa?

The most popular types of Fda jobs in Iowa are:

What are popular job titles related to Fda Contract jobs in Iowa?

For Fda Contract jobs in Iowa, the most frequently searched job titles are:

What job categories do people searching Fda Contract jobs in Iowa look for?

The top searched job categories for Fda Contract jobs in Iowa are:

What cities in Iowa are hiring for Fda Contract jobs?

Cities in Iowa with the most Fda Contract job openings:

Fda Contract jobs near you
Infographic showing various Fda Contract job openings in Iowa as of August 2026, with employment types broken down into 2% As Needed, 79% Full Time, 16% Part Time, 2% Contract, and 1% Nights. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $99,594 per year, or $47.9 per hour.

Packaging Supervisor- Mon-Thurs 4PM-2:30AM

Elanco

Fort Dodge, IA • On-site

Full-time

Posted 29 days ago

Elanco rating

7.8

Company rating: 7.8 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

50th 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: Leader, Packaging & Labeling

As the Leader, Packaging & Labeling, you will be part of the Manufacturing team supporting packaging operations at the Fort Dodge site. In this role, you will be responsible for leading day-to-day packaging operations, developing and coaching frontline employees, ensuring compliance with cGMP and safety standards, and driving operational excellence to deliver high-quality products.

Your Responsibilities:

  • Lead and supervise daily packaging and labeling operations to ensure safe, efficient, and compliant production.
  • Troubleshoot production issues, implement corrective actions, and drive continuous process improvements.
  • Coach, train, and develop employees on GMP requirements, safety procedures, technical processes, and company policies.
  • Partner with cross-functional teams to coordinate production activities, communicate operational updates, and support business objectives.
  • Ensure compliance with cGMP, OSHA, FDA, USDA, EU, and EPA regulations while administering company policies, safety programs, and union contract requirements.

What You Need to Succeed (minimum qualifications):

  • Education: Bachelor's degree with 1 year of relevant experience, associate's degree with 3 years of relevant experience, or High School Diploma/GED with 5 years of relevant experience.
  • Experience: A minimum of 5 years of experience in manufacturing, packaging, or production operations, preferably within a biological, pharmaceutical, or animal health manufacturing environment, with demonstrated leadership or supervisory experience.
  • Top 2 Skills: Leadership and coaching in a manufacturing environment, along with strong knowledge of packaging operations, cGMP compliance, and regulatory requirements (FDA, USDA, EU, and EPA).

What Will Give You a Competitive Edge (preferred qualifications):

  • Previous leadership experience in a packaging, labeling, or manufacturing environment within the pharmaceutical, biological, animal health, or other regulated industry.
  • Hands-on experience with packaging equipment, automated production systems, and SAP or other electronic manufacturing systems.
  • Strong knowledge of cGMP, FDA, USDA, OSHA, EU, and EPA regulations and experience supporting regulatory inspections and audit readiness.
  • Experience working in a union manufacturing environment with the ability to coach, develop, and lead frontline teams.
  • Demonstrated success driving continuous improvement initiatives, troubleshooting production issues, and improving safety, quality, and operational performance.

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 jobrelated 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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