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Medical Device Consulting Jobs in Iowa (NOW HIRING)

Our client is an American multinational information technology services and consulting company and ... Good understanding of Medical Device/ Pharma manufacturing process * Good understanding of ISA95 ...

... medical device, or clinical * Experience leading validation deliverables for GxP systems, including ... Work you'll do As a Senior Consultant, Regulatory, Risk, and Compliance on the Regulatory, Risk ...

... medical device, or clinical * Experience leading validation deliverables for GxP systems, including ... Work you'll do As a Senior Consultant, Regulatory, Risk, and Compliance on the Regulatory, Risk ...

... medical device, or clinical * Experience leading validation deliverables for GxP systems, including ... Work you'll do As a Senior Consultant, Regulatory, Risk, and Compliance on the Regulatory, Risk ...

... medical device, or clinical * Experience leading validation deliverables for GxP systems, including ... Work you'll do As a Senior Consultant, Regulatory, Risk, and Compliance on the Regulatory, Risk ...

... medical device, or clinical * Experience leading validation deliverables for GxP systems, including ... Work you'll do As a Senior Consultant, Regulatory, Risk, and Compliance on the Regulatory, Risk ...

... medical device, or clinical * Experience leading validation deliverables for GxP systems, including ... Work you'll do As a Senior Consultant, Regulatory, Risk, and Compliance on the Regulatory, Risk ...

Client Partner, Pharma

Des Moines, IA · On-site

$160K - $180K/yr

Deep understanding of life sciences companies (biopharma, medical device, CROs). * Experience ... Highly consultative, hands on and collaborative. * Excellent communication, presentation and ...

Showing results 21-40

Medical Device Consulting information

See Iowa salary details

$20

$46

$90

How much do medical device consulting jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for medical device consulting in Iowa is $46.81, according to ZipRecruiter salary data. Most workers in this role earn between $32.98 and $56.01 per hour, depending on experience, location, and employer.

What does a medical device consultant do?

A Medical Device Consultant provides expertise to companies developing, manufacturing, or marketing medical devices. They help navigate regulatory requirements, ensure compliance with FDA or EU MDR guidelines, conduct quality assessments, and offer strategic advice on product development. Consultants may also assist with clinical trials, risk management, and market entry strategies. Their goal is to help companies bring safe and effective medical devices to market efficiently while meeting industry regulations.

What are some typical daily responsibilities for professionals in medical device consulting?

Day-to-day tasks for Medical Device Consultants often include advising clients on regulatory strategy, preparing submissions for compliance agencies, assessing product safety and efficacy data, and coordinating with cross-functional teams such as R&D, quality assurance, and marketing. You may also conduct audits, lead training sessions, and assist clients in navigating clinical trial requirements or post-market surveillance. Collaboration and regular communication with client stakeholders are essential, as is staying current on evolving industry standards. This dynamic role provides exposure to diverse projects and the opportunity to make a tangible impact on the development and approval of innovative medical technologies.

What are the key skills and qualifications needed to thrive in medical device consulting?

To thrive in Medical Device Consulting, you need a strong background in biomedical engineering, regulatory knowledge, and experience with product development or commercialization, often supplemented by a relevant degree and industry certifications. Expertise with FDA regulations, ISO standards, clinical trial management systems, and common project management tools is highly valued. Exceptional problem-solving, client communication, and adaptability are crucial soft skills for success. These competencies are vital to effectively guide clients through compliance, market entry, and product lifecycle challenges in a complex, high-stakes industry.

How to become a medical device consultant?

To become a medical device consultant, individuals typically need a background in biomedical engineering, healthcare, or related fields, along with experience in medical device development, regulatory compliance, or quality assurance. Earning certifications such as ISO 13485 Lead Auditor or Regulatory Affairs Certification can enhance credibility, and strong project management and communication skills are essential for success in this role.

What are the most commonly searched types of Medical Device Consulting jobs in Iowa?

The most popular types of Medical Device Consulting jobs in Iowa are:

What are popular job titles related to Medical Device Consulting jobs in Iowa?

For Medical Device Consulting jobs in Iowa, the most frequently searched job titles are:

What job categories do people searching Medical Device Consulting jobs in Iowa look for?

The top searched job categories for Medical Device Consulting jobs in Iowa are:

Infographic showing various Medical Device Consulting job openings in Iowa as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $97,366 per year, or $46.8 per hour.

Opcenter Senior Modeler

TekWissen LLC

Des Moines, IA • On-site

$70/hr

Contractor

Re-posted 18 days ago


Job description

Overview:     
  
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. Our client is an American multinational information technology services and consulting company and is a leading provider of information technology, consulting, and business process outsourcing services, dedicated helping the world's leading companies build stronger businesses.   
  
  
Title: Opcenter Senior Modeler
Work Location: Des Moines, IA 50309
Duration: 12+ Months 
Job Type: Contract    
Work Type: Onsite
  
Job Description:  
  • Camstar/Opcenter Designer, Portal Studio, MIO, .NET, C#, HTLM5, CSS,Javscript, Sql/Oracle(Database), XML, ERP & Equipment Integration. OPC, IOT, PLC & SCADA, SQL queries
Must have Skills-
  • Must have Techno-Functional knowledge and hands-on experience on Siemens Opcenter/ Camstar application.
  • Must have End-to-End MES implementation experience for large global program using COTS Products like Opcenter/ Camstar.
  • Must worked on CAMSTAR designer and management studio
  • Worked with CAMSTAR Interoperability (CIO) / MOM module for equipment integration and ERP integration. Knowledge of Inbound and Outbound messaging
  • Good understanding of Medical Device/ Pharma manufacturing process
  • Good understanding of ISA95, MESA standards etc.
  • Experienced in Requirement Gathering, Design, specifications, and OT configurations specially for global programs.
  • Working experience with other functions such as functional team, system admins to ensure service availability and prompt issue resolution for key business efforts.
  • Must have experience of feasibility analysis to ensure recommended solutions meet the business requirements.
  • Standardize the solution to ensure reusability and supportability
  • Ability to work with cross functional and cross-cultural teams successfully
Good to have Skills:
  • Excellent leadership, Communication (Written and verbal) and interpersonal skills
  • Understanding of PLC and SCADA systems and OPC connectivity
  • Good knowledge of Hardware Network and Operating Systems
  • PowerBI Reporting tool and SQL knowledge
Roles and Responsibilities:
  • Lead team for architecture and MES MOM solution for Manufacturing Industry
  • Responsible for the design & development, Implementation and support of Opcenter (Camstar) MES applications
  • Requirement gathering, design and implementation of business processes in MES application
  • Lead feasibility analysis to ensure recommended solutions meet business requirements
  • CAMSTAR Interoperability (CIO) / MIO module ERP integration and for equipment integration.
  • Support the integration between MES, PLC/SCADA and other L1, L2 & L3 systems. Inbound and Outbound messaging flow.
  • Work closely with users to troubleshoot issues, and research methods of improving business processes.
  • Ability to communicate effectively with Client / Vendor to drive results.
  • Run efficient DevOps for platforms, products, or systems ensuring availability and optimal performance for responsible service area
  • Build and Guide the team members

Top skills:
  • Opcenter modelling
  • MES implementation experience
TekWissen® Group is an equal opportunity employer supporting workforce diversity. 

TekWissen logo

About TekWissen

Sourced by ZipRecruiter

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2009

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