Chemist I

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.

Job Summary:

The Chemist I position is designed for a developing chemist with basic scientific knowledge and understanding in laboratory techniques, analysis and problem solving. This position will work closely with other chemists and technicians to assist in the analysis of a wide range of customer samples and projects. The Chemist I is responsible for performing the analysis of sample materials using various analytical techniques to obtain both qualitative and quantitative data. This position also involves the use of analytical instrumentation to investigate the cause of chemical issues and problems.

Primary Responsibilities:

• Conduct chemical analysis and experiments in various fields, including organic, inorganic, and analytical chemistry.
• Support and handle samples for testing, ensuring adherence to standard operating procedures (SOPs) and experimental protocols.
• Assist in the development, testing and optimization of chemical processes and formulations.
• Support senior chemists and other team members with project-based work.
• Support the interpretation of experimental results and provide data driven conclusions.
• Document experimental procedures, results and data.
• Assist with the maintenance of laboratory instruments and other analytical tools ensuring calibration and accuracy.
• Ensure compliance with all relevant safety protocols, regulatory guidelines, and industry best practices.
• Continuously review and stay up to date with the latest scientific literature, emerging technologies, and industry trends.
• Any other duties and tasks as directed by the supervisor.

Education/Work Experience:

• Associate’s or Bachelor’s degree in relevant subject.
• 0-2 years of relevant experience.
• Working knowledge of compliance to a quality system (e.g., ISO 9001 and ISO 17025) preferred but not required.

Behaviors: Action-Oriented, Analytical Mindset, Approachability, Collaborative Leadership, Career Ambition, Composure, Courage, Customer Focus, Decision Quality, Detailed Oriented, Communication, Integrity & Trust, Interpersonal Savvy, Planning, Prioritizing, Time Management

Requirements:

• Basic knowledge and understanding of difficult sample collection, preparations, and the most advanced analytical methods. Ability to demonstrate full competency in all regulatory and non-regulatory sample workflows.
• Basic knowledge and understanding of complicated matrices from extractions of analytes and E&L.
• Basic knowledge and understanding of conventional and advanced quantitative methods.
• Basic knowledge and understanding of applicable instrumental and data interpretation software.
• Basic knowledge in method development and method validation.
• Ability to review analytical reports for accuracy, scientific content and readability.
• Ability to perform well under pressure and work with minimum supervision.
• Demonstrate the ability to perform work accurately and efficiently.
• Computer proficiency and experience with all MS products
• Computer skills proficiency and ability to learn new software.
• Detail-oriented self-starter with ability to manage multiple projects, work independently, and learn new disciplines.
• Excellent verbal and written communication skills.
• Demonstrates the drive and energy to be effective.

Supervisory Responsibilities: This position will have no supervisory responsibilities.

Work Environment & Physical RequirementsThis is a remote position. The employee is expected to maintain a dedicated, distraction-free home workspace with reliable high-speed internet access. Core working hours are determined by role responsibilities, client expectations, and business needs.

TravelThis role may require travel as business needs dictate, including overnight trips for client meetings, team collaboration, training sessions, and company events

Physical DemandsThe role involves prolonged periods of sitting and computer use, including frequent typing, video conferencing, and extended screen time. During travel or on-site activities, the employee may be required to stand or walk for extended periods, navigate office and client environments, and lift or carry materials or luggage up to 25 pounds.

Workspace & Accommodations The employee is responsible for maintaining a safe, ergonomic home workspace. Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions of this role.

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.

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