Who You Will Be Working For
Atlas is a global strategic consulting firm, focused on the life sciences industry. Our services include Management Consulting, Managed Services and Agile Services. Global pharmaceutical companies and emerging players in the Life Sciences depend on over four hundred Atlas consultants to ensure they have the capabilities that will give them the ability to succeed.
What You Will Do
We are seeking an experienced Compliance Engineer Consultant to support IT compliance and computer system validation activities for a global life sciences client. This role requires hands-on engineering experience executing validation work, supporting compliance documentation, and ensuring computer systems meet applicable quality, regulatory, and documentation standards. The ideal consultant will have experience working in a pharmaceutical compliance environment and will be comfortable performing ground-level execution work while partnering with IT, Quality, Compliance, and business stakeholders.
Job Responsibilities
* Perform computer system validation and IT compliance execution activities for regulated systems in a life sciences environment.
* Support validation deliverables including requirements, risk assessments, test protocols, test scripts, traceability matrices, deviation documentation, and validation summary reports.
* Execute testing and validation activities to confirm systems meet business, technical, quality, and regulatory requirements.
* Identify, document, and support resolution of non-conformances, deviations, compliance gaps, and documentation issues.
* Ensure documentation follows established compliance standards, templates, procedures, and approval workflows.
* Partner with IT, Quality, Compliance, business, and technical teams to understand system functionality, validation needs, and documentation expectations.
* Support review of system changes, enhancements, and releases to assess validation impact and required compliance activities.
* Maintain clear, accurate, audit-ready documentation aligned with applicable GxP, CSV, and quality standards.
* Provide hands-on engineering support for validation execution rather than only managing requirements or project activities.
* Communicate status, risks, issues, and documentation needs clearly to project stakeholders and leadership.
Qualifications
* Bachelor's degree in Engineering, Computer Science, Information Systems, Life Sciences, or a related field.
* Experience as an engineer supporting IT compliance, computer system validation, or regulated systems within the pharmaceutical or life sciences industry.
* Strong understanding of CSV, GxP, validation lifecycle activities, documentation standards, and quality procedures.
* Experience executing validation testing and preparing or reviewing validation documentation.
* Ability to understand system requirements, perform hands-on execution, and document results accurately.
* Experience identifying and documenting non-conformances, deviations, and compliance gaps.
* Strong attention to detail and ability to produce audit-ready documentation.
* Ability to work cross-functionally with IT, Quality, Compliance, business, and technical teams.
* Strong communication, analytical, and problem-solving skills.
* Ability to operate in a fast-paced consulting environment and support client priorities with accountability and professionalism.
Why Join the Atlas A-Team of Consultants
* Opportunity - Atlas has deep life sciences industry roots and a reputation with our clients for having superior quality consultants
* Meaningful Work - You will be part of the solution to help clients accomplish their patient first missions
* Culture - We are proactive, highly accountable, and high touch
* Solid - We have been delivering exceptional consulting talent for over 23 years
* Depth & Breadth of Collaborative Client Relationships – They depend on us to design strategic teams, which can produce and drive outcomes
* We are experts at Project Management, Portfolio Operations, Agile Services, Change Management and Talent/Organizational Design
* Benefits: Opportunity for a consulting career – average tenure of our consultants is over 2.5 years, with many here for over 7
* A-team of support behind you – We are all about making you successful
* Mutual trust – We build mutual trust and encourage respect and cooperation among team members
Send Us Your Resume
Send us your resume if you are exceptional and are interested in an opportunity to join a high growth management consulting firm. If you can answer yes to the below, let's talk:
Do you want to work on global pharmaceutical company initiatives?
Interested in joining a firm that has an extensive client base of leading life sciences companies, most of which are Fortune 100?
Do you have hands-on IT compliance or computer system validation experience in a regulated Life Sciences environment?
We Are an Equal Opportunity Employer
We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, genetics, disability, age, or veteran status. We value diversity and inclusion in our workplace and are committed to creating an environment where everyone has an equal opportunity to succeed.
