Codex Validation Group · 1 day ago
Validation Professional
Codex Validation Group (CVG) is an international consulting firm specializing in cGMP regulatory compliance and validation solutions for the Biotechnology, Pharmaceutical, and Medical Device industries. The Validation Professional will conduct validation activities, create and execute protocols, and ensure compliance with regulatory requirements while collaborating with cross-functional teams.
Medical Device
Responsibilities
Conducting validation activities
Creating and executing validation protocols
Ensuring compliance with regulatory requirements
Providing documentation for validation processes
Working closely with cross-functional teams to ensure the smooth qualification of facilities, utilities, equipment, and systems
Participating in problem-solving, risk management, and continuous improvement initiatives
Qualification
Required
Proficiency in cGMP, regulatory compliance, and industry standards, including FDA, ISO, GAMP 5, GLP, GMP, and 21 CFR Part 11
Experience with validation, including facilities, utilities, equipment, computerized systems, and critical process qualification
Strong skills in risk management, process optimization, and data analysis
Proven experience in documentation, protocol creation, and technical writing
Excellent problem-solving, analytical, and organizational abilities
Strong communication and teamwork skills to collaborate effectively with cross-functional teams
Bachelor's degree in Engineering, Life Sciences, or a related field
Preferred
Advanced certifications in validation or regulatory compliance are a plus
Experience in the Biotechnology, Pharmaceutical, or Medical Device industries is highly desirable
Company
Codex Validation Group
Codex Validation Group is an international consulting firm specializing in cGMP regulatory compliance, validation, automation, and engineering solutions for the Biotechnology, Pharmaceutical, and Medical Device industries.
Funding
Current Stage
Early StageCompany data provided by crunchbase