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Medical Device Startup Jobs in Indiana (NOW HIRING)

Pinnaql

HSE Manager

Lebanon, IN

We partner with pharmaceutical, biotech, and medical device organizations to navigate complexity ... Support commissioning, startup, and qualification activities from an HSE perspective. * Investigate ...

Pinnaql

HSE Manager

Lebanon, IN · On-site

We partner with pharmaceutical, biotech, and medical device organizations to navigate complexity ... Support commissioning, startup, and qualification activities from an HSE perspective. * Investigate ...

Pinnaql

HSE Manager

Lebanon, IN · On-site

We partner with pharmaceutical, biotech, and medical device organizations to navigate complexity ... Support commissioning, startup, and qualification activities from an HSE perspective. * Investigate ...

Novartis

Maintenance Technician

Indianapolis, IN · On-site

$47K - $88K/yr

Support 24x7 site-based operations after startup. Write/revise accurate operational procedures ... Previous pharmaceutical or medical device experience is preferred. Completed training in ...

Novartis

Maintenance Technician

Indianapolis, IN · On-site

$47K - $88K/yr

... startup. • Write/revise accurate operational procedures, training documents and maintenance ... medical device experience is preferred. • Completed training in radioactive or hazardous ...

Novartis

Maintenance Technician

Indianapolis, IN · On-site

$47K - $88K/yr

... startup. • Write/revise accurate operational procedures, training documents and maintenance ... medical device experience is preferred. • Completed training in radioactive or hazardous ...

Novartis

Maintenance Technician

Indianapolis, IN · On-site

$47K - $88K/yr

Support 24x7 site-based operations after startup. Write/revise accurate operational procedures ... Previous pharmaceutical or medical device experience is preferred. Completed training in ...

Syner-G

Sr. Project Manager

Indianapolis, IN

Drive HVAC startup, commissioning, qualification (IQ/OQ/PQ), and validation activities in alignment ... medical device) * Strong experience with HVAC systems, cleanroom environments, and facility ...

CAI

Computer Systems Validation Engineer

Indianapolis, IN · On-site

$75K - $106K/yr

We provide commissioning, qualification, validation, startup, project management, and other ... medical device In-depth understanding of GAMP guidelines and FDA regulations (21 CFR 11, 210, 211 ...

CAI

Computer Systems Validation Engineer

Indianapolis, IN · On-site

$75K - $106K/yr

We provide commissioning, qualification, validation, startup, project management, and other ... medical device In-depth understanding of GAMP guidelines and FDA regulations (21 CFR 11, 210, 211 ...

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All JobsMedical Device Startup JobsMedical Device Startup Jobs in Indiana

Medical Device Startup information

See Indiana salary details

$20

$34

$67

How much do medical device startup jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for medical device startup in Indiana is $34.94, according to ZipRecruiter salary data. Most workers in this role earn between $23.56 and $43.70 per hour, depending on experience, location, and employer.

What is the difference between Medical Device Startup vs Medical Device Engineer?

AspectMedical Device StartupMedical Device Engineer
Required CredentialsTypically requires engineering degree, certifications varyRequires engineering degree, often with specific certifications in biomedical or mechanical engineering
Work EnvironmentFast-paced, innovative startup setting, often small teamsDesign, develop, and test medical devices, usually in corporate or R&D labs
Employer & Industry UsageStartups in medical device industry, early-stage companiesEstablished companies, R&D departments, or startups
Common Search & Comparison IntentUnderstanding roles in startups, career optionsJob responsibilities, qualifications, career path

Medical Device Startup roles focus on innovation, product development, and often require versatile skills in a dynamic environment. Medical Device Engineers are specialized professionals responsible for designing and testing devices, typically within established or startup companies. While both roles require engineering credentials, startups emphasize adaptability and entrepreneurial spirit, whereas engineers focus on technical expertise and product quality.

What is a medical device startup?

A medical device startup is a company in its early stages that focuses on developing, manufacturing, and bringing innovative medical devices to market. These startups often work on new technologies or improvements to existing devices, aiming to address unmet medical needs or improve patient outcomes. They typically operate in a high-regulation environment and may seek funding from investors, grants, or partnerships to support research, development, and commercialization efforts. Success in this field requires multidisciplinary expertise, including engineering, regulatory affairs, and clinical knowledge.

What are the key skills and qualifications needed to thrive in a medical device startup, and why are they important?

To thrive in a medical device startup, you need a solid background in biomedical engineering, product development, and regulatory compliance, often supported by relevant degrees or experience in healthcare technology. Familiarity with FDA regulations, CAD design software, and project management tools like Jira or Asana is typically required. Strong collaboration, adaptability, and entrepreneurial problem-solving are essential soft skills in this dynamic environment. These skills and qualities are vital for navigating rapid innovation cycles, ensuring regulatory approval, and driving successful product launches in a competitive market.

What Are Jobs at a Medical Device Startup?

Jobs at a medical device startup include roles in research and development, sales, information technology, software development, and customer service. Working at a medical device startup in research and development, you collaborate with teams to design studies, perform research, and devise training materials for products. Your end goal is to help develop new products. As a sales representative, you promote and sell medical equipment, educate clients on the benefits of products, and respond to questions and concerns. Software and IT jobs at a medical device startup involve responsibilities like troubleshooting technical problems, diagnosing and repairing computer systems, creating databases, evaluating processes, and maintaining and utilizing medical imaging equipment.

What are the common challenges faced when working in a medical device startup environment?

Working in a medical device startup often involves navigating a fast-paced, dynamic environment where priorities can shift rapidly. Team members typically wear multiple hats, balancing product development with strict regulatory requirements and limited resources. Collaboration across engineering, clinical, and business teams is essential, as everyone works together to meet ambitious milestones and bring innovative products to market. Despite these challenges, the role provides unique opportunities to make a tangible impact and grow professionally within a close-knit, innovative team.
More about Medical Device Startup jobs
What are the most commonly searched types of Medical Device Startup jobs in Indiana? The most popular types of Medical Device Startup jobs in Indiana are:
What are popular job titles related to Medical Device Startup jobs in Indiana? For Medical Device Startup jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Medical Device Startup jobs in Indiana look for? The top searched job categories for Medical Device Startup jobs in Indiana are:
Medical Device Startup jobs near you

Senior CQV Engineer/Manager

IT Minds LLC

Indianapolis, IN • On-site

Other

Posted 29 days ago

Job description

Job Title: Senior CQV Engineer/Manager

Location: Remote / Hybrid / Onsite (Depending on Project Requirements)

Duration: Long-Term Contract

Position Overview

We are seeking an experienced CQV (Commissioning, Qualification & Validation) professional to support and lead validation activities within highly regulated pharmaceutical, biotechnology, and life sciences environments. This role will be responsible for ensuring GMP compliance across facilities, utilities, equipment, manufacturing processes, and computerized systems while driving validation strategies and project execution.

Key Responsibilities

  • Lead and support Commissioning, Qualification, and Validation (CQV) activities for facilities, utilities, equipment, laboratory systems, and manufacturing processes.
  • Develop and execute Validation Master Plans (VMPs), risk assessments, traceability matrices, and validation protocols.
  • Author, review, and approve IQ/OQ/PQ protocols and validation summary reports.
  • Coordinate commissioning and qualification activities for cleanrooms, HVAC systems, water systems (PW/WFI), clean steam, compressed gases, and manufacturing equipment.
  • Support FAT, SAT, startup, and operational readiness activities.
  • Manage deviations, investigations, CAPAs, and change controls.
  • Ensure compliance with FDA, EMA, MHRA, GAMP 5, Annex 11, 21 CFR Part 11, and Data Integrity requirements.
  • Collaborate with Engineering, Manufacturing, Quality Assurance, Automation, Regulatory Affairs, and Validation teams.
  • Support regulatory inspections, audits, and remediation activities.
  • Provide leadership and mentoring to validation engineers and CQV team members.

Required Qualifications

  • Bachelor's degree in Engineering, Life Sciences, Biotechnology, Pharmaceutical Sciences, or related field.
  • 10+ years of CQV / Validation experience within pharmaceutical, biotechnology, medical device, or life sciences industries.
  • Strong experience with GMP, cGMP, and regulatory compliance requirements.
  • Extensive hands-on experience with:
    • Commissioning, Qualification & Validation (CQV)
    • IQ / OQ / PQ Execution
    • Validation Master Plans (VMP)
    • Risk Assessments
    • Traceability Matrix Development
    • Deviation, CAPA, and Change Control Management
    • GMP Documentation and Compliance

Technical Experience Required

  • Cleanroom Qualification
  • HVAC Qualification
  • Water Systems (PW/WFI)
  • Clean Steam Systems
  • Compressed Air/Gas Systems
  • Manufacturing Equipment Qualification
  • Packaging Equipment Validation
  • Laboratory Equipment Qualification
  • Process Validation

Computer System Validation (CSV)

Experience validating one or more of the following systems:

  • MES
  • LIMS
  • Empower
  • TrackWise
  • Veeva
  • SAP
  • DeltaV
  • SCADA Systems
  • Laboratory Informatics Systems

Preferred Experience

  • Pharmaceutical or Biotechnology Manufacturing
  • Cell & Gene Therapy
  • Biologics Manufacturing
  • Vaccine Manufacturing
  • Greenfield Facility Startups
  • Large Capital Projects
  • Regulatory Inspection Readiness

Preferred Certifications

  • PMP
  • CQV / Validation Certifications
  • ASQ Certifications (CQE/CQA)
  • ISPE Training
  • Lean Six Sigma Green Belt or Black Belt

Must-Have Skills

  • CQV (Commissioning, Qualification & Validation)
  • GMP / cGMP Compliance
  • IQ/OQ/PQ
  • Validation Master Plans (VMP)
  • Risk Assessments
  • Traceability Matrix
  • CAPA & Deviation Management
  • Cleanroom / HVAC Qualification
  • Utilities Qualification (PW/WFI/Clean Steam)
  • Computer System Validation (CSV)
  • FDA / EMA / GAMP 5 Compliance

Best Regards,

Satya Satish J | Technical Recruiter | IT Minds LLC |

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