We Are Consultants and Advisors

We’re committed to being the place to work in life science compliance and regulation. The most passionate and high-performing consulting careers in the pharmaceutical, biotechnology, and medical device fields come together at RCA. Find out why so many other great healthcare consulting professionals are choosing careers with us.

Professionals First

Our people are “true professionals” and everyone has access to challenging work, competitive pay, and medical and insurance offerings. We offer variety and balance, and a remote-friendly workplace.

Diversity and Inclusion

We believe everyone at RCA should be themselves. Our diversity makes us stronger and our culture sets us apart. Our culture embraces diversity and we’re committed to creating a safe and inclusive workspace for everyone.

Meaningful Work

When you join RCA, you’ll be engaged in challenging work that provides technical and professional growth opportunities and allows you to collaborate with some of the best and brightest minds in regulatory compliance today.

Opportunities and Impact

We generate possibilities and unlock potential in ourselves and others. Our people positively impact our clients and stay laser-focused on delivering real results for our clients.

Virtual-Work Model

We're entering a new era of work and RCA is adapting to embrace this change. Our network has over 500 expert-level consultants, many of whom have a virtual-only work arrangement with the client.

High-Profile Clients

Our clients include dozens of Fortune 500 companies and the world’s most recognized brands. Delivering client satisfaction is important to everyone at RCA. We care about our clients’ problems and partner with them for impact and long-term, sustained success.

Recent Jobs

Quality Subject Matter Expert, Device

Description:
The Quality SME will be responsible for providing oversight of quality activities associated with medical devices, including manufacturing processes. The SME shall have experience directing, implementing, and maintaining quality management system implementation and improvement activities while ensuring compliance with ISO and GxP standards. The SME contributes to the completion of milestones associated with specific projects and supports ongoing quality assurance responsibilities.

Apply Now

Quality Subject Matter Expert, Pharma

Description:
The Quality SME will be responsible for providing oversight of quality activities associated with pharmaceuticals, including those associated with drug substance, drug product and finished product manufacturing processes. The SME shall have experience directing, implementing, and maintaining quality management system implementation and improvement activities while ensuring compliance with ISO and GxP standards. The SME contributes to the completion of milestones associated with specific projects and supports ongoing quality assurance responsibilities.

Apply Now

Regulatory Affairs Subject Matter Expert, Device

Description:
The Regulatory Affairs SME will be responsible for developing strategies and establishing policies according to business and client needs, both domestically and internationally. This position will provide direction and oversight to projects, advise clients on regulatory strategies, and submit final documentation to the FDA and/or other global regulatory agencies. Additionally, the role includes management of project teams supporting regulatory activities, including but not limited to, regulatory strategy which may include the identification of the device classification, the determination of applicable product codes, and testing requirements for the medical device submission activities (De Novo, 510(k) and PMA).

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Regulatory Affairs Subject Matter Expert, Pharma

Description:
The Regulatory Affairs SME will be responsible for developing strategies and establishing policies according to business and client needs, both domestically and internationally. This position will provide direction and oversight to projects, advise clients on regulatory strategies, and submit final documentation to the FDA and/or other global regulatory agencies. Additionally, the role includes management of project teams supporting regulatory filings for the FDA, Health Canada, and the EMA (including electronic filings with FDA).

Apply Now

The Application Process

Apply to the job for you

We’ll get to know each other

Meet our team

Apply to the jobs that you match and provide us with some general information about your background, education, work history and relevant experiences. These include full-time and independent contractor opportunities.

The application process usually includes a series of virtual chats and in-depth interviews, and potentially a brief online assessment. This is also an opportunity for you to understand if the role and the company are right for you.

If you join RCA, our onboarding team will walk you through benefits, insurance, compensation, and so on. Then you’ll be a part of our team!

View all job openings

What Our People Are Saying

Our people are the heartbeat of our firm. Our talented and diverse teams are focused on delivering our purpose and making things better for our customers and colleagues. They make this a great place to work.

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