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Contract Medical Device Jobs in Indiana (NOW HIRING)

... contract analytics platforms, or revenue intelligence software. * Knowledge of subscription pricing and escalation frameworks. _____ About FDB: FDB is the leading provider of drug and medical device ...

... contract analytics platforms, or revenue intelligence software. * Knowledge of subscription pricing and escalation frameworks. _____ About FDB: FDB is the leading provider of drug and medical device ...

... contract analytics platforms, or revenue intelligence software. * Knowledge of subscription pricing and escalation frameworks. _____ About FDB: FDB is the leading provider of drug and medical device ...

... contract analytics platforms, or revenue intelligence software. * Knowledge of subscription pricing and escalation frameworks. _____ About FDB: FDB is the leading provider of drug and medical device ...

... contract analytics platforms, or revenue intelligence software. * Knowledge of subscription pricing and escalation frameworks. _____ About FDB: FDB is the leading provider of drug and medical device ...

... contract analytics platforms, or revenue intelligence software. * Knowledge of subscription pricing and escalation frameworks. _____ About FDB: FDB is the leading provider of drug and medical device ...

... contract analytics platforms, or revenue intelligence software. * Knowledge of subscription pricing and escalation frameworks. _____ About FDB: FDB is the leading provider of drug and medical device ...

... contract analytics platforms, or revenue intelligence software. * Knowledge of subscription pricing and escalation frameworks. _____ About FDB: FDB is the leading provider of drug and medical device ...

... contract analytics platforms, or revenue intelligence software. * Knowledge of subscription pricing and escalation frameworks. _____ About FDB: FDB is the leading provider of drug and medical device ...

... contract analytics platforms, or revenue intelligence software. * Knowledge of subscription pricing and escalation frameworks. _____ About FDB: FDB is the leading provider of drug and medical device ...

... contract analytics platforms, or revenue intelligence software. * Knowledge of subscription pricing and escalation frameworks. _____ About FDB: FDB is the leading provider of drug and medical device ...

... contract analytics platforms, or revenue intelligence software. * Knowledge of subscription pricing and escalation frameworks. About FDB: FDB is the leading provider of drug and medical device ...

... contract analytics platforms, or revenue intelligence software. * Knowledge of subscription pricing and escalation frameworks. About FDB: FDB is the leading provider of drug and medical device ...

Showing results 21-40

Contract Medical Device information

See Indiana salary details

$20

$47

$91

How much do contract medical device jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for contract medical device in Indiana is $47.42, according to ZipRecruiter salary data. Most workers in this role earn between $33.41 and $56.73 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a contract medical device engineer?

To thrive as a Contract Medical Device Engineer, you need strong expertise in biomedical engineering, regulatory standards (like ISO 13485 or FDA 21 CFR Part 820), and product development processes, typically supported by a relevant engineering degree. Familiarity with CAD software, risk management tools, and quality management systems is essential, and certifications such as Six Sigma or PMP can be advantageous. Excellent problem-solving, project management, and communication skills help you collaborate effectively with cross-functional teams and clients. These skills and qualifications ensure devices are developed safely, efficiently, and in full compliance with industry regulations.

What is a contract medical device professional?

A Contract Medical Device professional is a specialist who works on a temporary or project-based basis within the medical device industry. These professionals may be hired by companies to assist with tasks such as regulatory compliance, product development, quality assurance, or clinical trials. Their expertise helps organizations meet regulatory requirements, ensure product safety, and bring new medical devices to market efficiently. Contract roles are ideal for companies needing specialized knowledge for a specific project or limited time frame.

What are some common challenges faced by contract medical device professionals and how can they be addressed?

Contract medical device professionals often navigate challenges such as adjusting quickly to different company cultures, learning new product lines rapidly, and staying up-to-date with evolving regulatory standards. To address these, it's helpful to maintain strong communication with team members, proactively seek clarification on project expectations, and invest time in ongoing professional development. Being adaptable and building a network of industry contacts can also support success in various contract assignments.
What are the most commonly searched types of Medical Device jobs in Indiana? The most popular types of Medical Device jobs in Indiana are:
What are popular job titles related to Contract Medical Device jobs in Indiana? For Contract Medical Device jobs in Indiana, the most frequently searched job titles are:
What cities in Indiana are hiring for Contract Medical Device jobs? Cities in Indiana with the most Contract Medical Device job openings:
Infographic showing various Contract Medical Device job openings in Indiana as of July 2026, with employment types broken down into 60% Full Time, 22% Part Time, 1% Temporary, and 17% Contract. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution, with an average salary of $98,641 per year, or $47.4 per hour.

Global GxP Quality Project Manager - Pharmaceutical (Hybrid - Indianapolis, IN) Contract

Pharmavise

Indianapolis, IN • On-site

Contractor

Re-posted 17 days ago


Job description


Our Fortune 500 global Pharmaceutical client is seeking an experienced Global GxP Quality Project Manager.
Job Summary:
The Global GxP Project Manager will support enterprise-level Global Quality Transformation and Technology initiatives. This role operates within Global Quality leadership and supports strategic transformation efforts across Quality Culture, Quality Maturity Systems, and global QMS modernization. The scope is global and not site-specific. The organization requires a structured, transformation-driven PM who understands regulated environments, Lean deployment, and digital Quality enablement.
Key Responsibilities:
  • Lead global GxP Quality transformation programs across multiple sites and functions

  • Drive QMS harmonization and enterprise process standardization initiatives

  • Support inspection readiness modernization and alignment with FDA expectations

  • Optimize CAPA and Deviation lifecycle processes through structured improvement efforts

  • Deploy Lean methodologies within Quality functions to improve efficiency and reduce waste

  • Support implementation or enhancement of digital Quality systems (Veeva QMS, TrackWise, MasterControl)

  • Lead initiatives involving digital logbooks, eBR, MES integration, and Quality data analytics

  • Enable development of Quality Maturity metrics, dashboards, and executive reporting tools

  • Drive automation and AI-enabled improvements in Quality workflows where applicable

  • Provide structured governance, PMO alignment, and milestone tracking

  • Manage cross-functional stakeholder engagement across Quality, Regulatory, Manufacturing, and Technology

  • Identify and mitigate program risks in a global, regulated environment

  • Prepare executive-level updates and KPI dashboards for senior leadership

Required Qualifications:
  • 8-10+ years of experience in pharmaceutical and/or medical device industries

  • Bachelor's degree in a scientific, life sciences, or health-related field

  • Strong GxP knowledge (GMP, FDA Quality Systems Regulations)

  • Experience leading enterprise-level Quality or QMS transformation initiatives

  • Experience supporting global or multi-site programs

  • Demonstrated Lean deployment or process improvement experience

  • Strong stakeholder management and executive communication skills

  • Ability to work onsite in Indianapolis, IN

Preferred Qualifications:
  • PMP certification

  • Lean certification (Lean Six Sigma Green Belt or Black Belt preferred)

  • Experience with Veeva QMS, TrackWise, or MasterControl

  • Drug and medical device experience

  • Experience supporting inspection readiness or regulatory scrutiny

Other Details:
Schedule: Full Time