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Biomedical Project Manager Jobs in Indiana (NOW HIRING)

Imaging Service Coordinator

Indianapolis, IN ยท Hybrid

$19 - $24/hr

Bachelor's degree in engineering technology, biomedical engineering, or business/project management preferred but not required . Physical Requirements: * Physical ability to lift/carry up to 50 lbs ...

Manufacturing Engineer

Warsaw, IN ยท On-site

$70K - $90K/yr

... project assignments and complete work in a timely manner Good problem-solving skills using quality ... Leads continuous improvement initiatives, manages change controls, troubleshoots cleaning problems ...

Help drive/ lead continuous improvement projects. * Ensure team members are up to date and trained ... Three or more years combined industry (biomedical, medical device) and/or military experience.

Senior Manufacturing Engineer

Pierceton, IN ยท On-site

$84K - $115K/yr

Manages multiple tasks/projects and schedules priorities for self and manufacturing engineers ... Bachelor's degree in Mechanical Engineering or Biomedical Engineering. * Minimum of seven years ...

Senior Manufacturing Engineer

Pierceton, IN ยท On-site

$84K - $115K/yr

Manages multiple tasks/projects and schedules priorities for self and manufacturing engineers ... Bachelor's degree in Mechanical Engineering or Biomedical Engineering. * Minimum of seven years ...

Senior Manufacturing Engineer

Pierceton, IN ยท On-site

$84K - $115K/yr

Manages multiple tasks/projects and schedules priorities for self and manufacturing engineers ... Bachelor's degree in Mechanical Engineering or Biomedical Engineering. * Minimum of seven years ...

Postdoctoral Appointee

Bloomington, IN ยท On-site

$45K - $61K/yr

... project planning, data interpretation, authorship of presentations and publications, lab management ... The Department of ACBP conducts cutting-edge biomedical research across a wide range of diseases ...

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Biomedical Project Manager information

See Indiana salary details

$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 cities in Indiana are hiring for Biomedical Project Manager jobs? Cities in Indiana with the most Biomedical Project Manager job openings:
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.

Validation Engineering Roles

BW Filling & Closing

Indianapolis, IN โ€ข On-site

Full-time

This job post hasย expired 1 day ago.ย Applications are no longer accepted.


Job description

Validation Engineering Roles

Join one of our 45 offices in the US as part of a committed team of over 1500 professionals, working directly with clients on projects that shape the world around us. As a contract professional with BW Design Group, you'll be welcomed into a rapidly growing business and empowered to make an immediate impact. You'll work alongside seasoned leaders, technical specialists, and subject matter experts within our Regulatory Compliance Practice to deliver the highest quality solutions with consistency and accuracy.

You'll support both capital project CQV delivery and individual technical contribution solutions for our clients within the Life Sciences industry. You'll help clients implement critical changes to improve their performance and realize their most important goals through:

  • Validation & Compliance Activities: Assist basic and conceptual design phases of capital projects by working with clients and vendors on embedding compliance, testability and lifecycle thinking into early design. Establish User Requirement Specifications for critical equipment and systems. Assess risk across various aspects of systems' functions and focus efforts on critical quality aspects. Develop and execute validation and FDA compliance related documents/protocols for pharmaceutical equipment and processes โ€“ employing industry's most progressive Digital Validation Tools. Prepare, execute, and manage commissioning and qualification documents for utility, facility, and process equipment. Perform FAT, SAT, IQ, and OQ documentation development and execution on Automated Systems. Conduct investigations and troubleshoot validation-related issues. Prepare comprehensive written validation reports.
  • Project Management & Leadership: Lead all aspects of client relationship development and project execution. Develop project plans, strategies, and manage project resources, budgets, and schedules. Oversee complete project lifecycle from concept through design, implementation, installation, commissioning, and startup. Manage multiple project responsibilities simultaneously with excellent organizational skills. Focus on project success related to scope, schedule, budget, and client satisfaction.

What You'll Bring

Experience Requirements (Based on Role Level):

โ€ข Validation Engineer II: Minimum 2-7 years project experience with validation of automation, packaging, drug substance (i.e., pooling, centrifugation, TFF) and/or drug product (i.e., filling, inspection) systems/equipment, utilities, and/or facilities in pharmaceutical or medical device environments

โ€ข Sr. Validation Engineer: Minimum 7+ years demonstrated experience with design, commissioning, validation of automation, packaging drug substance (i.e., pooling, centrifugation, TFF) and/or drug product (i.e., filling, inspection) systems/equipment, utilities, and/or facilities in pharmaceutical or medical device environments validation

โ€ข Sr. Project Manager: Minimum 10+ years project engineering, design engineering, or project management experience with packaging, processing, automation, or Life Science applications.

Technical Skills & Qualifications: Bachelor's degree in Engineering (Bioengineering, Biomedical, Chemical, Electrical, Mechanical, or equivalent technical degree) Validation experience in automation, packaging, general drug substance and/or drug product systems/equipment, computer systems, utilities, and/or facilities Strong technical writing and oral communication skills Proficiency with project documentation and computer skills (Microsoft Office, Microsoft Project, AutoCAD) Experience with entire project lifecycle from concept development through startup (preferred)

Professional Attributes: Excellent leadership and organizational skills with ability to manage multiple responsibilities Outstanding communication and interpersonal skills to interact with all levels of management, clients, and vendors Flexibility with tasks and strong analytical capabilities Willing and able to travel as necessary for project requirements including installation, startup activities, client meetings, and industry events.

Barry-Wehmiller is an equal opportunity employer. M/F/D/V This organization uses E-Verify.Applicants may be subject to pre-employment screening which may include drug screening, reference checks, employment verifications, background screening and/or skills assessments.