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Biotechnology Project Manager Jobs in Wheaton, IL

JLL

Senior Facilities Manager

Chicago, IL

Coordinate and oversee capital improvement projects, working with engineering teams, contractors ... pharmaceutical, biotech, or similarly regulated environments * Demonstrated expertise in GMP ...

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Biotechnology Project Manager information

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How much do biotechnology project manager jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for biotechnology project manager in Wheaton, IL is $44.69, according to ZipRecruiter salary data. Most workers in this role earn between $38.80 and $49.04 per hour, depending on experience, location, and employer.

What does a biotechnology project manager do?

A Biotechnology Project Manager oversees and coordinates projects within the biotechnology industry, ensuring that research and development initiatives, product launches, or clinical trials are completed on time and within budget. They work with cross-functional teams, including scientists, engineers, and regulatory experts, to set project goals, manage resources, and monitor progress. Their responsibilities also include risk management, stakeholder communication, and ensuring compliance with industry regulations. This role is vital for driving innovation and bringing new biotech products or solutions to market efficiently.

What are the key skills and qualifications needed to thrive as a biotechnology project manager, and why are they important?

To thrive as a Biotechnology Project Manager, you need a solid background in biological sciences or engineering, project management expertise, and often an advanced degree such as an MSc or PhD. Familiarity with tools like Microsoft Project, Gantt charts, regulatory compliance systems, and certifications such as PMP are commonly required. Strong leadership, communication, and problem-solving skills set exceptional candidates apart in managing cross-functional teams and complex timelines. These skills and qualities are essential to effectively coordinate scientific projects, ensure regulatory compliance, and deliver successful outcomes in a dynamic biotech environment.

What are some common challenges faced by biotechnology project managers in cross-functional team environments?

Biotechnology Project Managers often work with multidisciplinary teams composed of scientists, regulatory specialists, manufacturing experts, and business development professionals. One common challenge is ensuring clear communication and alignment across these diverse groups, especially when technical jargon or differing priorities create misunderstandings. Additionally, managing project timelines in a highly regulated environment, where unexpected trial results or compliance issues may cause delays, requires strong adaptive planning. Successful Biotechnology Project Managers foster collaboration by setting clear goals, conducting regular check-ins, and proactively addressing potential roadblocks.

What is the difference between Biotechnology Project Manager vs Research Scientist?

AspectBiotechnology Project ManagerResearch Scientist
Required CredentialsBachelor's or Master's in Biotechnology, Project Management certification often preferredMaster's or PhD in Biotechnology or related field
Work EnvironmentProject teams, corporate labs, industry settingsResearch labs, academic institutions, industry research divisions
Employer & Industry UsageBiotech companies, pharmaceutical firms, biotech startupsUniversities, research institutes, biotech companies

The main difference is that a Biotechnology Project Manager oversees project planning, coordination, and execution within biotech companies, focusing on timelines and budgets. In contrast, a Research Scientist conducts experiments and develops new biotech products or knowledge. Both roles require strong biotech credentials, but their daily tasks and focus areas differ significantly.

What are popular job titles related to Biotechnology Project Manager jobs in Wheaton, IL?

For Biotechnology Project Manager jobs in Wheaton, IL, the most frequently searched job titles are:

What job categories do people searching Biotechnology Project Manager jobs in Wheaton, IL look for?

The top searched job categories for Biotechnology Project Manager jobs in Wheaton, IL are:

What cities near Wheaton, IL are hiring for Biotechnology Project Manager jobs?

Cities near Wheaton, IL with the most Biotechnology Project Manager job openings:

Biotechnology Project Manager jobs near you

Project Manager - Class III Medical Implants

ProPharma Group

Western Springs, IL • On-site

Full-time

Re-posted 16 days ago

Job description

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.
The Project Manager for Class III Medical Implants is responsible for leading cross-functional teams through the full lifecycle of highly regulated, risk-critical medical device programs. This role drives project planning, execution, regulatory alignment, and commercialization activities to ensure safe, effective, and compliant implantable medical products reach the market on time and within budget.
Key Responsibilities
1. Project Leadership & Execution
  • Lead end-to-end project management from concept through design, verification/validation, clinical evaluation, regulatory submission activities including PMA preparation, IDE clinical studies, and global regulatory pathways (FDA, EU MDR) where applicable.
  • Develop and maintain integrated project plans, schedules, budgets, and risk registers.
  • Facilitate cross-functional project team meetings (R&D, Quality, Regulatory, Manufacturing, Clinical, Marketing).
  • Manage project KPIs, timelines, and resource allocations; escalate risks proactively.

2. Design & Development Oversight
  • Drive implementation of design controls compliant with 21 CFR 820, ISO 13485, and ISO 14971 risk management requirements: user needs, design inputs/outputs, verification, validation, design transfer.
  • Collaborate with engineering teams to ensure design requirements are met for implantable use (biocompatibility, sterilization, packaging, durability).
  • Support planning and execution of clinical studies or physician evaluations when required.

3. Manufacturing & Supply Chain Coordination
  • Partner with operations/manufacturing teams to develop scalable, validated production processes.
  • Ensure suppliers meet quality and regulatory standards for implantable components.
  • Support process validation (IQ/OQ/PQ) and device master record (DMR) creation.

4. Stakeholder & Communication Management
  • Communicate project status, milestones, risks, and decision needs to executives and key stakeholders.
  • Serve as the primary point of contact for project-related inquiries.

Qualifications
Education
  • Bachelor's degree required (Engineering, Life Sciences, or related field preferred).
  • Master's degree or PMP certification a plus.

Experience
  • 5+ years of project management experience in medical devices; Class III or implantable medical device development experience strongly preferred, including PMA or IDE programs.
  • Demonstrated familiarity with regulatory frameworks for high-risk medical devices.
  • Experience in cross-functional leadership and complex product development.

Skills & Competencies
  • Deep understanding of design controls, risk management, and medical device quality systems.
  • Excellent organizational and planning skills.
  • Strong interpersonal and communication skills.
  • Ability to manage ambiguity and drive decision-making.
  • Expertise using project management tools (MS Project, Smartsheet, or similar).

**Remote working with 20% onsite in Effingham, IL
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.
Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

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