Job Description

RQM+ is The MedTech CRO, accelerating innovation to patient impact. Our tailored solutions deliver regulatory and quality expertise, FDA-recognized laboratory services, clinical trials, and reimbursement strategies across device types and therapeutic areas to bring life-changing technologies to patients -- faster, safer, better.

We don't make MedTech. We make MedTech happen.

Our experienced teams are cohesive, collaborative, and proactive, constantly seeking to improve and evolve while remaining laser-focused on customer success. RQM+ elevates the MedTech experience through best-in-class service and clear, concise communication. We serve as an extension of our customers establishing and maintaining excellent client and site relationships and providing direct access to our technology platforms for real-time data and study transparency

The Staff Toxicologist will play a critical role in authoring and guiding toxicological risk assessments for medical devices and combination products. This position involves performing high-level biological safety evaluations, providing strategic input on regulatory submissions, and mentoring junior staff members as needed. The Staff Toxicologist will serve as a subject matter expert and will collaborate closely with internal teams and external stakeholders to ensure the safety and compliance of products.

Primary Responsibilities:

Perform toxicological risk assessments for chemical characterization, extractables/leachables (E&L) data, and other safety evaluations for medical devices and drug-device combination products, including literature reviews, computational modeling, and risk assessment strategies. Coordinate and collaborate with internal laboratories to review and interpret test lab reports and ensure high-quality data for regulatory submissions. Guide regulatory submissions for FDA (CDRH) and EU MDR compliance, with a focus on navigating and meeting regional and global requirements. Act as the primary point of contact for regulatory agencies and serve as an expert in all matters related to medical device toxicology. Contribute to the development of new protocols, strategies, and methodologies for toxicological assessments in line with evolving industry standards and regulatory requirements. Mentor and provide technical guidance to junior toxicologists as needed, ensuring high-quality work and adherence to regulatory standards. Present complex toxicological data to cross-functional teams, senior leadership, and external stakeholders in a clear, concise, and actionable manner. Participate in initiatives to improve internal processes, with a focus on enhancing efficiency, compliance, and the overall effectiveness of the toxicology department. Provide expert input for the development and implementation of training programs and resources to enhance the team's knowledge and performance.

Requirements:

Master's degree or equivalent in Toxicology or a related field. Board Certified (DABT) Toxicologist or actively pursuing certification. 4-6 years of relevant experience in toxicology, with at least 3 years specifically focused on medical device toxicological risk assessments and regulatory submissions. Advanced experience with regulatory submissions or exposure to industry-specific toxicology studies. Advanced knowledge of global regulatory environments and emerging trends in medical device toxicology. Familiarity with toxicology databases and software tools. Knowledge of Good Laboratory Practice (GLP) or other quality assurance standards. Proven experience in developing and leading toxicological evaluations for medical devices, including chemical characterization and biological safety evaluations. Strong working knowledge of ISO 10993, ISO 18562, FDA (CDRH) regulations, and EU MDR requirements. Extensive experience with chemical characterization testing, extractables/leachables studies, and risk assessment processes. Experience with direct interaction and communication with regulatory agencies (FDA, EU) is highly preferred. Strong technical writing experience, particularly in regulatory submissions, safety assessments, and scientific reports. Strong leadership skills with the ability to mentor, guide, and inspire a team of toxicologists. Highly organized with excellent problem-solving skills, capable of managing multiple projects and deadlines with high performance orientation. Strong verbal and written communication skills with the ability to present complex scientific data in an accessible and persuasive manner. Advanced computer skills, including proficiency in Microsoft Office Suite and toxicological databases/software. Adapts to change when directed. Excellent interpersonal communication and influencing skills as well as experience working collaboratively with clients and employees. Provides clear and appropriately detailed project updates. Ability to escalate to management when needed. Requires willingness to work a flexible schedule

Behaviors:

Customer Focus, Action-Oriented, Approachability, Building Effective Teams, Business Acumen, Career Ambition, Composure, Courage (Managerial), Decision Quality, Informing, Integrity & Trust, Interpersonal Savvy, Planning, Time Management

Supervisory Responsibilities:

Work Environment/Physical Demands

This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones, photocopiers and filing cabinets. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee is occasionally required to sit; climb or balance; and stoop, kneel, crouch or crawl. The employee must frequently lift or move objects up to 10 pounds and occasionally lift or move objects up to 25 pounds.

Being an industry leader in Medtech is just the beginning for RQM+. We consider our employees our biggest asset and we invest heavily in ongoing learning and development. Providing a rewarding place to work is rooted deep in our core values. From an industry leading compensation package to a deeply engrained focus on work life balance, RQM+ has a unique offering for regulatory and quality professionals. At RQM+, you are not just another employee, you are a member of RQM+ family. Make your impact today!

We invite you to apply if you have an interest in learning more about our organization and beginning your journey with us.

Job Opportunity Verification

At RQM+, we prioritize the security of our job applicants. To ensure a safe application process:
All legitimate RQM+ job opportunities are listed on our official careers page: rqmplus.com/careers
Every candidate going through the interview process will participate in a voice and/or video interview.
Exercise caution with unsolicited job offers or requests for sensitive information.

This job operates in a professional office environment in a global organization. This role routinely uses standard office equipment such as computers, phones, photocopiers, and filing cabinets. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee is occasionally required to sit; climb or balance; and stoop, kneel, crouch, or crawl.

We are committed to promoting equality of opportunity for all staff and job applicants. We aim to create a working environment in which all individuals can make best use of their skills, free from discrimination or harassment, and in which all decisions are based on merit.

Our selection for recruitment does not discriminate based on age, disability, gender reassignment, marital or civil partner status, pregnancy or maternity, race, color, nationality, ethnicity, ethnic or national origin, religion or belief, sex or sexual orientation or gender reassignment status (protected characteristics).