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Biomedical Project Manager Jobs in Indiana (NOW HIRING)

Kymanox

(Contract) CQV Engineer

Indianapolis, IN · On-site

The ideal candidate will have a bachelor's degree in a science-related field such as Biomedical ... Kymanox provides professional services related to engineering, compliance, and project management.

Azenta

SPS Lab Process Engineer

Indianapolis, IN · On-site

$79K - $99K/yr

Bachelor's degree in Engineering (Chemical, Mechanical, Biomedical, Industrial, or related field ... Project management experience Physical Requirements * Reaching, lifting, bending * Ability to lift ...

Azenta

SPS Lab Process Engineer

Indianapolis, IN · On-site

$79K - $99K/yr

Bachelor's degree in Engineering (Chemical, Mechanical, Biomedical, Industrial, or related field ... Project management experience Physical Requirements * Reaching, lifting, bending * Ability to lift ...

EHOB INC

Product Development Engineer

Indianapolis, IN · On-site

Define and manage testing and prototyping equipment as needed * Support project, material, and ... Bachelor of Science or higher in Design, Industrial Design, Mechanical Engineering, Biomedical ...

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Biomedical Project Manager information

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$20

$44

$72

How much do biomedical project manager jobs pay per hour?

As of Jun 5, 2026, the average hourly pay for biomedical project manager in Indiana is $44.00, according to ZipRecruiter salary data. Most workers in this role earn between $38.22 and $48.27 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Biomedical Project Manager, and why are they important?

To thrive as a Biomedical Project Manager, you need a solid background in biomedical sciences or engineering, project management experience, and often a relevant degree such as a BS/MS in a related field. Familiarity with project management software (e.g., MS Project, Asana), regulatory compliance systems (like FDA or ISO standards), and sometimes a PMP certification are typically important. Outstanding communication, leadership, and problem-solving skills help you coordinate cross-functional teams and manage stakeholder expectations. These competencies ensure successful project delivery, regulatory compliance, and effective collaboration in the complex biomedical industry.

How does a Biomedical Project Manager typically collaborate with cross-functional teams during a project lifecycle?

A Biomedical Project Manager works closely with diverse teams such as research scientists, regulatory specialists, engineers, and clinical staff to ensure project milestones are met. They facilitate communication across these groups by organizing regular meetings, tracking progress, and resolving issues that arise. This collaborative approach helps align project objectives, address challenges promptly, and maintain compliance with regulatory standards. Effective coordination and relationship-building are key to successfully delivering complex biomedical projects on time and within budget.

What are Biomedical Project Managers?

Biomedical Project Managers are professionals responsible for overseeing and coordinating biomedical research projects, clinical trials, or product development within the healthcare or life sciences industry. They ensure that projects are completed on time, within budget, and in compliance with regulatory standards. Their role involves managing teams, communicating with stakeholders, and addressing potential risks or issues during the project lifecycle. Biomedical Project Managers often work closely with scientists, engineers, medical staff, and regulatory bodies to facilitate successful project outcomes.

What is the difference between Biomedical Project Manager vs Biomedical Engineer?

AspectBiomedical Project ManagerBiomedical Engineer
Required CredentialsBachelor's or Master's in Biomedical Engineering, Project Management CertificationBachelor's or Master's in Biomedical Engineering or related field
Work EnvironmentProject teams, clinical settings, R&D departmentsLaboratories, manufacturing, clinical research
Employer & Industry UsageHospitals, biotech firms, medical device companiesMedical device companies, research institutions, hospitals

The Biomedical Project Manager focuses on overseeing projects, coordinating teams, and ensuring timely delivery of biomedical products. In contrast, the Biomedical Engineer is involved in designing, developing, and testing medical devices or systems. While both roles require biomedical engineering knowledge, the project manager emphasizes management skills and project execution, whereas the engineer concentrates on technical development and innovation.

What are popular job titles related to Biomedical Project Manager jobs in Indiana? For Biomedical Project Manager jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Biomedical Project Manager jobs in Indiana look for? The top searched job categories for Biomedical Project Manager jobs in Indiana are:
What cities in Indiana are hiring for Biomedical Project Manager jobs? Cities in Indiana with the most Biomedical Project Manager job openings:
Biomedical Project Manager jobs near you
Infographic showing various Biomedical Project Manager job openings in Indiana as of May 2026, with employment types broken down into 92% Full Time, 6% Part Time, and 2% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $91,525 per year, or $44 per hour.
(Contract) CQV Engineer

(Contract) CQV Engineer

Kymanox

Indianapolis, IN • On-site

Contractor

Posted 18 days ago

Job description

This posting is for a potential future role as we proactively build our talent pipeline. As new opportunities arise, we'll review applicants and reach out to those whose experience aligns with our hiring needs.
Job Description:
Is Kymanox the right fit for you?
You want to make a difference and have an impact...
You enjoy having an influence in your day-to-day work...
You are motivated by working alongside a team filled with
subject matter experts who will help you learn and grow...
You wake up every day and do what you do
... because patients deserve better.
If this sounds like you, you've come to the right place.
The (Contract) CQV Engineer will have direct experience in Commissioning, Qualification or Validation.
Responsibilities:
  • Author, execute, and summarize commissioning and qualification deliverables including FAT/SAT, IQ, OQ, PQ protocols and reports for process equipment, clean utilities (WFI, clean steam, gases), HVAC/cleanrooms, and automated systems.
  • Apply risk-based CQV approach in accordance with ASTM E2500, ICH Q9, and ISPE Baseline Guides.
  • Perform field execution: system walkdowns, punch-list resolution, functional testing, loop checks, and startup support.
  • Generate, investigate, and resolve deviations; support change control and CAPA processes in electronic quality systems.
  • Author traceability matrices linking URS critical aspects testing.
  • Collaborate daily with Engineering, Quality, Automation, Manufacturing, and client stakeholders.
  • Provide technical input during design reviews and risk assessments (FMEA, PHA).
  • Support validation maintenance activities (periodic review, re-qualification, change control impact assessments).
  • Lead small to medium subsystems or work packages under guidance of a senior CQV lead.
Educational Background:
The ideal candidate will have a bachelor's degree in a science-related field such as Biomedical Engineering, Mechanical Engineering or Chemical Engineering.
Experience:
  • 5 years of hands-on CQV experience in pharmaceutical, biotechnology, and/or medical device industries
  • Direct experience executing IOQ/PQ on automated equipment (filling lines, isolators, lyophilizers, device assembly equipment strongly preferred)
  • Proven ability to author and execute qualification protocols independently
  • Strong working knowledge of cGMP (21 CFR 210/211, Part 11, EU Annex 11), ASTM E2500, GAMP 5, and ISPE guidelinesExperience with electronic documentation and quality management systems
  • Excellent technical writing, organization, and communication skills
Desired Aptitude and Skill Set:
  • Proven ability to develop validation strategy independently
  • Detail-oriented
  • Highly organized
  • Excellent written and oral English communication skills
  • Excellent problem-solving skills
  • Seasoned soft skills
  • Team player
  • IT and technology savvy
  • Understanding of FDA's CGMPs (i.e., Quality Systems)
Travel:
Up to 50% travel is possible for onsite client CQV support
Compensation:
Hourly rate is commensurate with experience, qualifications, and other intangibles evident during the interview process - as well as market conditions
About Kymanox:
Join Kymanox - a life sciences professional services company dedicated to life sciences who has successfully delivered over 4000 projects across 20+ countries. Become a member of a dynamic, fulfilling team that helps a broad range of life science products get to market more quickly, more affordably, and with the highest quality and safety standards possible in today's biotechnology, pharmaceutical, medical device, and combination product industries. With a reputation of providing unparalleled professional services and our highly collaborative team of engineering, compliance, and project management experts, Kymanox provides an outstanding opportunity for learning and career advancement. Kymanox encourages team members, especially new graduates, and young professionals, to work on a variety of projects to gain increased learnings in Kymanox's service offerings and the life science industry as a whole.
Kymanox is looking for motivated individuals who want to solve problems in the life science industries while doing the work they love and helping get modern medicines that enhance and save patient lives to market. Kymanox provides professional services related to engineering, compliance, and project management. We service clients ranging from Fortune 100 companies to virtual start-up companies. The company was founded in 2004 and has been growing steadily since its inception. Our corporate HQ is based in Research Triangle Park, NC.
To learn more about our company, please visit our website: Life Science Solutions | Kymanox
Kymanox is an equal-opportunity employer and works diligently to protect the rights of job seekers by following all local, state, and federal laws as well as best Human Resource (HR) practices in the Life Science industry.
Employment Type: Contractor

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