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Manager Fda Consulting Jobs in Park Ridge, IL (NOW HIRING)

Ventura Solutions LLC

Sales Engineer

Barrington, IL · On-site +1

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Regulatory knowledge related to FDA and MDR compliance is required; combination products experience ... On the consulting side, we integrate seamlessly into your team and manage small to complex ...

Ventura Solutions LLC

Sales Engineer

Barrington, IL · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Regulatory knowledge related to FDA and MDR compliance is required; combination products experience ... On the consulting side, we integrate seamlessly into your team and manage small to complex ...

Bond Consultants Group

Be Seen First

Import Coordinator - (Import/Export Exp needed)

Wood Dale, IL · On-site

$19 - $22/hr

  • Medical

  • Dental

  • PTO

Customs and Border Protection, and other agencies such as the FDA, ensuring accurate and timely ... Manage payments to terminals (e.g., PierPass, PayCargo) * Maintain accurate shipment records and ...

Sinai Chicago

RESEARCH IRB COORDINATOR

Chicago, IL · On-site

... consulting with the IRB Chair or the RTO Manager where appropriate. • Supports FDA-regulated IND and IDE trials by ensuring IRB processes align with 21 CFR Parts 312 and 814 requirements, including ...

Sinai Chicago

RESEARCH IRB COORDINATOR

Chicago, IL

... consulting with the IRB Chair or the RTO Manager where appropriate. · Supports FDA-regulated IND and IDE trials by ensuring IRB processes align with 21 CFR Parts 312 and 814 requirements, including ...

ICONMA

Technical writer

Lake Forest, IL · On-site

Consulting (Project Delivery, SOW), etc. Our Staff Members Our in-house team offers a broad range ... Our Recruiting Management and staff members at ICONMA understand that our greatest assets are our ...

Mindful TMS Neurocare Centers

Be Seen First

TMS Technician

Wheaton, IL · On-site

$38K - $45K/yr

... manager. Primary responsibilities are, but not limited to: · Providing educational consultations ... FDA-Approved, non-invasive, non-systemic treatment for severe depression, OCD, and more. At our ...

Abbott

Sr. Project Manager

Lake Forest, IL · On-site

$55 - $57/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... R&D, and FDA regulated products. * Proven leadership skills, results oriented, highly ... Consultants Eligible Benefits Upon Waiting Period: * Medical and Prescription Drug Plans * Dental ...

Certified Group

Lab Analyst

Aurora, IL · On-site

... consulting firm offering expert guidance, training, and auditing support across FDA, USDA, and ... Accurately perform and read test results and notify Laboratory Management of deviations * Prepare ...

Certified Group

Lab Analyst

Aurora, IL · On-site

... consulting firm offering expert guidance, training, and auditing support across FDA, USDA, and ... Accurately perform and read test results and notify Laboratory Management of deviations * Prepare ...

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Showing results 21-40

All JobsFda Consulting JobsManager Fda Consulting JobsManager Fda Consulting Jobs in Park Ridge, IL

Manager Fda Consulting information

What does a manager in FDA consulting do?

A Manager in FDA consulting oversees projects and teams that help clients navigate the regulatory requirements set by the U.S. Food and Drug Administration (FDA). Their responsibilities include advising companies on compliance, preparing submissions, and developing strategies to obtain FDA approvals for products such as drugs, medical devices, and food items. They also ensure clients are up-to-date with changing regulations and help resolve any regulatory issues that may arise. This role requires strong project management skills, deep regulatory knowledge, and the ability to communicate complex requirements to clients.

How does a manager in FDA consulting typically collaborate with cross-functional teams to ensure regulatory compliance for clients?

As a Manager in FDA Consulting, you'll frequently work alongside experts from regulatory affairs, quality assurance, clinical research, and product development to guide clients through complex compliance challenges. This often involves facilitating meetings, interpreting FDA guidelines, and coordinating the preparation of submission documents. Strong communication skills are essential, as you'll translate regulatory requirements into actionable strategies for diverse teams. Collaboration is key to ensuring all stakeholders are aligned and that client deliverables meet both regulatory and business objectives.

What are the key skills and qualifications needed to thrive as a manager in FDA consulting, and why are they important?

To thrive as a Manager in FDA Consulting, you need a deep understanding of FDA regulations, compliance strategies, and industry best practices, typically supported by a relevant degree and experience in regulatory affairs. Familiarity with regulatory submission systems like eCTD, and certifications such as RAC (Regulatory Affairs Certification), are commonly required. Strong leadership, problem-solving abilities, and excellent communication skills set top performers apart in this role. These competencies ensure clients receive effective guidance through complex regulatory processes, minimizing compliance risks and expediting product approvals.

What is the difference between Manager Fda Consulting vs Regulatory Affairs Specialist?

AspectManager Fda ConsultingRegulatory Affairs Specialist
CredentialsTypically requires a bachelor's or master's in life sciences, with experience in FDA regulationsUsually holds a bachelor's degree in life sciences or related field, with certification preferred
Work EnvironmentConsulting firms, client sites, or remote; project-based workIn-house or pharmaceutical/medical device companies; regulatory departments
Industry UsageCommonly employed in consulting firms advising multiple clientsPrimarily employed within companies managing regulatory submissions

While both roles require knowledge of FDA regulations, a Manager Fda Consulting typically leads consulting projects and advises clients, whereas a Regulatory Affairs Specialist manages regulatory submissions within a company. The roles differ mainly in scope, environment, and responsibilities, but share core regulatory knowledge.

What job categories do people searching Manager Fda Consulting jobs in Park Ridge, IL look for?

The top searched job categories for Manager Fda Consulting jobs in Park Ridge, IL are:

What cities near Park Ridge, IL are hiring for Manager Fda Consulting jobs?

Cities near Park Ridge, IL with the most Manager Fda Consulting job openings:

Manager Fda Consulting jobs near you
Infographic showing various Manager Fda Consulting job openings in Park Ridge, IL as of August 2026, with employment types broken down into 81% Full Time, 17% Part Time, 1% Contract, and 1% Nights. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution.

Sales Engineer

Ventura Solutions LLC

Barrington, IL • On-site, Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 15 days ago

Job description

Ventura Solutions is a leading consulting, staffing, and training firm specializing in the medical device and combination products industry. We help companies accelerate product development and ensure market compliance.

We are seeking a dynamic and results-driven Medical Device Sales Engineer to drive the growth of our consulting, staffing, and training services. The ideal candidate will have a solid background in the medical device industry, combined with strong business development skills. This role requires identifying and qualifying leads, building long-term client relationships, and delivering customized service solutions that align with client needs.

Responsibilities

  • Lead Generation & Prospecting: Identify and qualify potential clients in the medical device and combination products sectors.
  • Client Engagement: Build and maintain relationships with R&D, Quality, and Regulatory teams to understand their challenges and position Ventura Solutions’ services as tailored solutions.
  • Sales Pipeline Management: Manage the sales funnel, including initial outreach, follow-ups, scheduling meetings, and closing deals.
  • Solution Selling: Articulate the value of our consulting, staffing, and training services in areas such as product development, design controls, risk management, quality systems, and regulatory compliance.
  • Proposal Development: Collaborate with internal teams to create detailed scopes of work and negotiate contracts that align with client needs.
  • Industry Expertise: Leverage knowledge of medical device product development processes to identify opportunities where Ventura Solutions can add value, including support for FDA and MDR compliance.
  • Networking & Industry Presence: Represent Ventura Solutions at industry conferences, networking events, and webinars to promote our services and expand our client base.

Qualifications

  • Bachelor’s degree in engineering or a scientific discipline (e.g., biomedical engineering, mechanical engineering, or related field).
  • Minimum of 2 years of experience in the medical device industry, with exposure to product development, manufacturing, regulatory, and quality systems.
  • Understanding of the medical device product development and post-market surveillance process.
  • Regulatory knowledge related to FDA and MDR compliance is required; combination products experience is preferred but not mandatory.
  • Proven track record in business development, sales, or client-facing roles, preferably within consulting or staffing services, is preferred but not mandatory. 
  • Excellent communication, negotiation, and interpersonal skills, with the ability to build rapport with technical and non-technical stakeholders.
  • Self-motivated and goal-oriented, with strong organizational and time-management skills.

Why Join Ventura Solutions?

  • Be part of a growing company that is making an impact in the medical device and combination products industry.
  • Good work life balance, flexible hours, and opportunities to attend industry events nationwide.
  • Competitive salary, performance-based incentives, and opportunities for professional growth.

If you’re passionate about helping companies bring innovative medical devices to market and thrive in a dynamic sales environment, we’d love to hear from you!

Location

  • Lake Barrington, IL or Remote for the right candidate

Employment Type

  • Full-time

Compensation and Benefits

  • $60k-$120k plus bonus and commission (unlimited earning potential - no current cap on commission)
  • Choice of medical, dental, and vision plans
  • Paid vacation time
  • 401(k)

About Ventura Solutions

Ventura Solutions is a reputable end-to-end medical device and combination product consulting, staffing, and training firm. With our deep industry expertise spanning medical devices and combination products, coupled with an outstanding talent pool, we stand out as the preferred option for a diverse array of projects. On the consulting side, we integrate seamlessly into your team and manage small to complex Statement of Work (SOW) projects. On the staffing side, we help source, screen, and on-board reputable employees to fill temporary, temp to permanent, and permanent job openings. We accelerate product development, keep products compliant, and help build great organizations. For more information, visit us at www.ventura-solutions.com.

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