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Project Manager Biology Jobs in Indiana (NOW HIRING)

Freudenberg

Project Manager

Jeffersonville, IN

Provide technical and project-management leadership, set priorities, allocate tasks, mentor team ... Qualifications: * Bachelor's/University degree in Engineering, Chemistry, Biology, or related ...

Pacelabs

Client Project Manager 1

Indianapolis, IN · On-site

$50K/yr

Client ProjectManager Compensation:$50,000 per year Hours:Monday through Friday, 8:00 AM - 5:00 PM ... Bachelor's degree in business administration, chemistry, biology, or a related field, or an ...

Ivy Tech

Full-time Faculty - Biology

South Bend, IN · On-site

Manage a classroom environment conducive to student learning and in adherence to federal, state ... projects related to college and program accreditations, and grant related projects. Support and ...

Ivy Tech

Full-time Faculty - Biology

South Bend, IN · On-site

Manage a classroom environment conducive to student learning and in adherence to federal, state ... projects. • Support and engage with Ivy CareerLink and Development (Ivy Tech Foundation). • ...

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Showing results 1-20

All JobsProject Biology JobsProject Manager Biology JobsProject Manager Biology Jobs in Indiana

Project Manager Biology information

See Indiana salary details

$36.6K

$97.7K

$154.2K

How much do project manager biology jobs pay per year?

As of Jul 15, 2026, the average yearly pay for project manager biology in Indiana is $97,708.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,700.00 and $117,000.00 per year, depending on experience, location, and employer.

Can I be a project manager with a biology degree?

A biology degree can qualify you for a project manager role in scientific or research settings, especially if combined with skills in leadership, organization, and communication. Relevant certifications like PMP or experience managing projects can enhance your prospects in this field.

What is the highest paying project manager?

In the field of biology, project managers with advanced degrees, specialized knowledge, and certifications such as PMP or PMI-ACP tend to earn higher salaries. Senior project managers overseeing large, complex research projects or working in pharmaceutical or biotech industries often have the highest compensation, which can exceed $120,000 annually depending on experience and location.

What are the typical daily responsibilities of a Project Manager Biology?

As a Project Manager Biology, your daily responsibilities often include coordinating project timelines, managing cross-functional teams, monitoring budget and resource allocation, and ensuring regulatory compliance. You'll regularly communicate with stakeholders such as scientists, laboratory staff, and external partners to keep projects on track and resolve challenges as they arise. Additionally, you'll be tasked with documenting progress, preparing status reports, and identifying areas for process improvement. This role offers a dynamic environment where effective multitasking and strong problem-solving skills are essential for success.

What are the key skills and qualifications needed to thrive in the Project Manager Biology position, and why are they important?

To thrive as a Project Manager Biology, you need a solid background in biological sciences, project management experience, and often a degree in biology or a related field. Familiarity with project management software (such as MS Project or Asana), regulatory compliance systems, and certifications like PMP or PRINCE2 is valuable. Strong leadership, communication, and organizational skills are crucial for effectively coordinating multidisciplinary teams. These competencies ensure that complex biological projects are delivered on time, within scope, and in compliance with scientific and regulatory standards.

What is a Project Manager Biology job?

A Project Manager Biology oversees research projects in the biological sciences, coordinating teams, timelines, and resources to ensure successful project execution. They work in industries such as pharmaceuticals, biotechnology, or academia, managing budgets, compliance, and communication between stakeholders. Their role bridges scientific expertise with project management skills to drive research goals efficiently.

How to become a biotech project manager?

To become a biotech project manager, candidates typically need a bachelor's degree in biology, biotechnology, or a related field, along with experience in project management and the biotech industry. Certifications such as PMP (Project Management Professional) can enhance prospects, and strong skills in leadership, communication, and regulatory knowledge are essential. Gaining experience in laboratory or research settings and understanding biotech tools and processes are also beneficial.

What biology jobs pay over $100k?

Project managers in biology, especially those overseeing research teams or managing large projects, can earn over $100,000 annually. Senior roles such as research directors, biotech executives, and regulatory affairs managers also typically have salaries exceeding this threshold, often requiring advanced degrees and extensive experience. Skills in leadership, budgeting, and regulatory compliance are valuable in these high-paying positions.
What are popular job titles related to Project Manager Biology jobs in Indiana? For Project Manager Biology jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Project Manager Biology jobs in Indiana look for? The top searched job categories for Project Manager Biology jobs in Indiana are:
Project Manager Biology jobs near you
Infographic showing various Project Manager Biology job openings in Indiana as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $97,708 per year, or $47 per hour.

Project Manager

Freudenberg

Jeffersonville, IN

Full-time

Re-posted 6 hours ago

Job description

Working at Freudenberg: We will wow your world!

Responsibilities:

  • Lead development of accuratemanufacturing cost models, make-vs-buy decisions, work-center costs, and support quote generation and pricing strategy for new business or large sustaining initiatives.

  • Establish, track, and report key performance metrics for development, project progression, and launch; champion continuous-improvement and Lean/Six Sigma activities to boost quality, delivery, and cost.

  • Gather and translate user, customer, clinician, and/or market needs and inputs into clear product and business requirements; present data-driven recommendations to stakeholders.

  • Maintain project documentation in line with internal procedures and notified-body expectations, supporting audits and ensuring robust change-control and traceability. Prepare reports and project summaries to communicate the status of projects on a regular basis.

  • Provide technical and project-management leadership, set priorities, allocate tasks, mentor team members, and foster a culture of efficiency, innovation, and regulatory excellence across the organization.

  • Manages a few discrete projects with teams, operating within a defined PDP process delivering to achieve defined scope, schedule, and budget performance goals.

  • Familiarity with and managing efforts for compliance with ISO standards, country-specific (FDA, MDR, Health Canada, PMDA, etc.), GMP regulations, and customer requirements.

  • Input and review for design history files, device master records, risk analyses, and validation protocols/reports (IQ/OQ/PQ) to ensure designs, processes, equipment, and products meet client, regulatory, and business needs.

Qualifications:

  • Bachelor's/University degree in Engineering, Chemistry, Biology, or related science/technical field.

  • 3+ years' experience in Medical Device or related industry

  • 2+ years' experience in leading teams in a manufacturing or engineering environment, with demonstrated experience of managing work within a project plan framework, including managing a schedule, budget, scope, progress, and reporting.

  • Understanding of scientific principles and manufacturing processes used in medical device production, such as running equipment, injection molding, extrusion, catheter manufacturing, and assembly, including the materials used.

  • Demonstrated experience with formal problem-solving methodologies, critical thinking, and deductive skills.

  • Understanding of ISO standards, particularly ISO 13485, ISO 14001, ISO 14971, and 45001. Knowledge of GMP principles and their application in medical device manufacturing, including country-specific regulatory requirements (i.e., 21 CFR 820 in the United States, and EU MDR).

  • Demonstrated experience using Lean/Six Sigma tools as necessary for new and continuous improvement projects.

  • Demonstrated experience providing leadership and managing multiple projects of low to medium complexity.

The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.

Freudenberg Medical LLC

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