Overview
On Site
USD 125,000.00 - 150,000.00 per year
Full Time
Skills
Management
Documentation
Collaboration
Development Testing
Data Integrity
Continuous Improvement
Auditing
Mentorship
Lifecycle Management
Computerized System Validation
Life Sciences
Clinical Research
GxP
Regulatory Compliance
Software Development Methodology
Agile
Relational Databases
Oracle
SQL
Communication
Problem Solving
Conflict Resolution
Organizational Skills
Project Management
Pharmaceutics
Cloud Computing
Job Details
Lead Validation Specialist
Location: Remote (Preference for East Coast candidates)
Salary: $125,000-$150,000/year + bonus potential About the Role
We're seeking an experienced Lead Validation Specialist with a strong background in clinical systems and computer systems validation to join our growing team. In this role, you'll lead validation initiatives to ensure that all systems are compliant with GxP regulations and 21 CFR Part 11, working closely with developers, QA professionals, and SMEs to support rapid development timelines without compromising quality or compliance.
This is an ideal position for someone who thrives in a fast-paced, dynamic environment, enjoys mentoring others, and is eager to take ownership of validation strategy and execution in a regulated life sciences setting.
What You'll Do
Preferred Qualifications:
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
#M2
#LI-AJ1
#DI-AJ1
Ref: #558-Scientific
Location: Remote (Preference for East Coast candidates)
Salary: $125,000-$150,000/year + bonus potential About the Role
We're seeking an experienced Lead Validation Specialist with a strong background in clinical systems and computer systems validation to join our growing team. In this role, you'll lead validation initiatives to ensure that all systems are compliant with GxP regulations and 21 CFR Part 11, working closely with developers, QA professionals, and SMEs to support rapid development timelines without compromising quality or compliance.
This is an ideal position for someone who thrives in a fast-paced, dynamic environment, enjoys mentoring others, and is eager to take ownership of validation strategy and execution in a regulated life sciences setting.
What You'll Do
- Lead and manage the validation team, ensuring systems meet compliance with GxP and 21 CFR Part 11.
- Develop, execute, and maintain validation strategies and documentation for clinical systems.
- Collaborate cross-functionally with developers, QA, and SMEs to support validated environments.
- Ensure data integrity and adherence to ALCOA+ principles across relational databases (Oracle, MS SQL).
- Drive continuous improvement of validation processes to maintain audit-readiness and efficiency.
- Mentor and coach team members to promote excellence in validation and regulatory compliance.
- Support the implementation and lifecycle management of new and existing clinical systems.
- Bachelor's degree required.
- 8+ years of professional experience in computer systems validation within life sciences or clinical research.
- 5+ years leading a validation team or similar function.
- Proven expertise with GxP and 21 CFR Part 11 compliance.
- Experience with SDLC, Agile methodologies, and validation of cloud-based systems.
- Strong technical foundation with relational databases (Oracle, MS SQL).
- Excellent communication, problem-solving, and organizational skills.
- Ability to work independently in a remote, fast-paced, and collaborative environment.
Preferred Qualifications:
- Prior project management experience.
- Experience in a CRO, biotech, or pharmaceutical environment.
- Familiarity with cloud technologies and web-based systems.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
#M2
#LI-AJ1
#DI-AJ1
Ref: #558-Scientific
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.