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Temp Medical Device Startup Jobs in Kansas (NOW HIRING)

Intellectt INC

Process Engineer

Kansas City, KS · On-site

... medical device, or other regulated manufacturing environments. The role will support manufacturing ... installation, and startup activities. * Monitor process performance and implement process ...

Elwood Staffing

Kit Assembler

Chanute, KS

$17/hr

Temp-to-Hire position * $17.00 /hour * Full Time work available * First Shift (Monday through Friday from 07:00am to 03:30pm) * Assemble and prepare medical device kits according to production ...

New

TekWissen LLC

QA Technician

Lenexa, KS · On-site

$20 - $23/hr

Temporary Assignment Work Type: Onsite Shift: Monday-Friday 08:00 AM to 04:30 PM Summary The QA ... Background in Medical device, cGMP, or ISO certified environment. * Data entry skills and ...

Aerotek

Quality Assurance Technician

Olathe, KS

$24 - $26/hr

Work Environment Work in a medical device manufacturing facility within a QC department that ... If eligible, the benefits available for this temporary role may include the following: * Medical ...

New

Engenious Design

Integrated Marketer

Prairie Village, KS · On-site

$17.75/hr

... medical device leaders and talented recruits. You'll work with a team to set strategy, manage ... This is a full-time, non-temporary position. This position works from our Kansas City based design ...

Engenious Design

Integrated Marketer

Prairie Village, KS · On-site

$17.75/hr

... medical device leaders and talented recruits. You'll work with a team to set strategy, manage ... This is a full-time, non-temporary position. This position works from our Kansas City based design ...

ICL

Process Control Engineer

Lawrence, KS · On-site

$76K - $131K/yr

The engineer will lead and support control system projects from concept through startup, while also ... Individuals with temporary visas such as E, F-1 (including those with OPT or CPT), H-1, H-2, L-1, B ...

NinjaOne

Senior Software Engineer, Java

Kansas, KS · On-site +1

... startup environment. Impact product more hands on than at other companies, building software of ... We have you covered with our comprehensive benefits package, which includes medical, dental, and ...

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All JobsMedical Device Startup JobsTemp Medical Device Startup JobsTemp Medical Device Startup Jobs in Kansas

Temp Medical Device Startup information

What are some typical challenges faced by temp employees at a medical device startup, and how can they successfully adapt?

Temp employees at medical device startups often encounter fast-paced environments with evolving priorities and limited onboarding time. They may need to quickly familiarize themselves with complex products, regulatory standards, and cross-functional teams. Successful adaptation involves being proactive in asking questions, embracing flexibility, and staying organized to manage shifting tasks. Building strong communication with permanent staff can also help temp employees integrate smoothly and deliver impactful results.

What is a temp medical device startup?

A Temp Medical Device Startup is a temporary or short-term company focused on developing, testing, or launching new medical devices. These startups often form to rapidly innovate or address specific healthcare needs, sometimes as part of a contract or pilot project. Temporary startups may operate only for the duration of a specific development cycle or clinical trial, after which they may dissolve or be absorbed by a larger company. Working at such a startup typically involves fast-paced, cross-functional teamwork and the opportunity to contribute to cutting-edge healthcare solutions.

What are the key skills and qualifications needed to thrive as a temp at a medical device startup?

To thrive as a Temp at a Medical Device Startup, you need a background in life sciences or engineering, familiarity with regulatory standards, and the ability to rapidly learn new processes. Experience with tools like CAD software, laboratory equipment, or project management systems is often required, along with knowledge of FDA or ISO compliance. Strong problem-solving skills, flexibility, and effective communication help you adapt to the fast-paced and evolving environment of a startup. These competencies are crucial for ensuring product quality, meeting deadlines, and supporting innovation in a highly regulated and competitive field.

What is the difference between Temp Medical Device Startup vs Medical Device Quality Assurance Technician?

AspectTemp Medical Device StartupMedical Device Quality Assurance Technician
CredentialsTypically requires a degree in engineering, biology, or related field; certifications varyRequires a degree in life sciences or engineering; often holds certifications like CQE or ISO auditor
Work EnvironmentFast-paced, dynamic startup setting, often temporary or project-basedStructured environment within established companies, focusing on compliance and quality control
Employer & Industry UsageCommon in early-stage startups developing new medical devicesFound in established medical device companies ensuring product quality and regulatory compliance

While both roles involve working with medical devices, a Temp Medical Device Startup typically focuses on supporting early-stage product development in a dynamic environment. In contrast, a Medical Device Quality Assurance Technician works within established companies to ensure products meet quality standards and regulatory requirements.

What job categories do people searching Temp Medical Device Startup jobs in Kansas look for? The top searched job categories for Temp Medical Device Startup jobs in Kansas are:
What cities in Kansas are hiring for Temp Medical Device Startup jobs? Cities in Kansas with the most Temp Medical Device Startup job openings:
Temp Medical Device Startup jobs near you
Infographic showing various Temp Medical Device Startup job openings in Kansas as of August 2026, with employment types broken down into 64% Full Time, 18% Part Time, 5% Temporary, 9% Contract, and 4% Nights. Highlights an 100% In-person job distribution.

Process Engineer

Intellectt INC

Kansas City, KS • On-site

Contractor

Re-posted 12 days ago

Job description

Job Title: Process Engineer

Location: Greater Kansas City Area, Kansas
 

Job Summary:

We are seeking a Process Engineer with 3–7 years of experience in pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments. The role will support manufacturing operations for a monoclonal antibody (mAb) production facility, focusing on process optimization, equipment troubleshooting, commissioning, qualification, validation, and continuous improvement activities.

Key Responsibilities
  • Provide technical support for manufacturing processes and equipment.
  • Troubleshoot process and equipment-related issues on the production floor.
  • Support commissioning, qualification, and validation of manufacturing equipment and systems.
  • Assist with capital projects, including equipment design, installation, and startup activities.
  • Monitor process performance and implement process improvements.
  • Perform root cause investigations and support CAPA, Change Control, and Deviation activities.
  • Ensure compliance with cGMP, quality standards, and regulatory requirements.
  • Create and maintain engineering documents such as P&IDs, PFDs, URS, and qualification protocols.
  • Support SIP (Steam-In-Place) and CIP (Clean-In-Place) systems.
  • Collaborate with Manufacturing, Quality, Validation, and Engineering teams.
Required Skills:
  • Process Engineering
  • Process Troubleshooting
  • Commissioning, Qualification & Validation (CQV)
  • SIP/CIP Systems
  • P&IDs and PFDs
  • GMP / cGMP Compliance
  • Root Cause Analysis (RCA)
  • CAPA, Change Control, and Deviation Management
  • Data Analysis and Continuous Improvement
Required Qualifications:
  • Bachelor’s Degree in Engineering, Biotechnology, Chemical Engineering, Mechanical Engineering, or related Science discipline.
  • 3–7+ years of experience in Pharmaceutical, Biotechnology, Medical Device, or other regulated industries.
  • Experience working in a cGMP-regulated manufacturing environment.
Strong problem-solving, communication, and teamwork skills.