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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 Senior Chemist I is designed for an experienced, independent chemist and will perform laboratory analyses and support scientific data interpretation. This role will be responsible for conducting a variety of analyses, interpreting data, and developing technical reports for customer projects. The Senior Chemist I will leverage strong scientific knowledge and experience to ensure accurate and efficient testing while maintaining a focus on meeting client and internal standards. This role requires the ability to work autonomously with minimal supervision, while still collaborating effectively with laboratory teams and other departments to meet project goals.

Primary Responsibilities:

• Perform laboratory experiments to develop, optimize, and validate analytical methods (HPLC, GC, LCMS, GCMS).

• Prepare and analyze samples for routine testing, stability studies, and in-process controls, ensuring accuracy and reproducibility.

• Operate, calibrate, and maintain analytical instruments (e.g., HPLC, GC, LCMS, GCMS) and troubleshoot issues to minimize downtime.

• Support advanced analysis and writing of challenging, complex customer projects and related business needs.

• Collaborate with Laboratory Chemists, Study Directors, and Research & Development teams to ensure alignment with project goals and timelines.

• Review and assess data for trends and discrepancies and suggest improvements where applicable.

• Ensure compliance with regulatory guidelines, laboratory safety protocols, and best practices during all laboratory activities.

• Maintain thorough documentation of experimental procedures, results, and data interpretations.

• Contribute to the development of laboratory methods and procedures.

• Provide technical support and mentorship to junior team members as needed.

• Act as support on primary review report writing process and finalization.

• Champion laboratory safety protocols, regulatory compliance, and adherence to industry best practices, continuously evaluating and improving safety measures in the lab.

• Keep up to date with the latest scientific literature, emerging technologies, and industry innovations, ensuring that the laboratory maintains a competitive edge in scientific advancements.

• Any other duties and tasks as directed by the supervisor.

Education/Work Experience:

• Bachelor’s Degree in relevant field with 5+ years’ experience; Master’s 0-3 years’ experience.

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:

• Proficiency in performing and interpreting laboratory experiments using techniques such as HPLC, GC, LCMS, GCMS.

• Advanced knowledge and understanding of analytical method development.

• Advanced knowledge and understanding of investigative and regulatory techniques.

• Advanced practitioner of all scientific methods and troubleshooting.

• Advanced practitioner of all software with a deep understanding of settings and features.

• Ability to be innovative and use the software to solve problems.

• 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.

Salary: $80,000-$100,000

Work Environment & Physical Requirements: This role is based in a laboratory setting and involves regular use of lab equipment, instrumentation, and standard safety protocols. The employee is regularly required to stand for extended periods, and may need to bend, reach, kneel, or crouch to access equipment or samples. This role typically involves lifting or carrying items up to 25 lbs, with occasional lifting up to 25 lbs, and may require the use of personal protective equipment (PPE).

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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