. Education & Experience: Bachelor's degree in Biochemistry, Chemical Engineering, LifeSciences, or a related scientific...
, and corporate quality teams. Requirements: Bachelor's degree in lifesciences or related field. Minimum of 8 years of experience...
Roles & Responsibilities: Develop quality assurance documentation for new product development and regulatory submissions. Maintain and improve quality system processes by identifying and correcting deficiencies. Engage in design, develo...
Job Description: We are seeking an experienced Method Validation Engineer to support the development, validation, and implementation of analytical methods—primarily dissolution and particulate matter testing (USP 788 )—for a GMP release ...
, and corporate quality teams. Requirements: Bachelor's degree in lifesciences or related field. Minimum of 8 years of experience...
in a life science or technical discipline, preferably in engineering, bioengineering, biology, or chemistry 2-5 years...
Responsibilities: The Regulatory Coordinator is responsible for the coordination, preparation, and maintenance of regulatory documentation and compliance for clinical trials. This role ensures adherence to local, state, and federal regul...
Summary : Supports testing and validation activities for medical devices, ensuring compliance with regulatory and quality standards. Roles & Responsibilities : Prepare test samples and fixtures for mechanical and functional testing. E...
Job Description: Reports directly to Engineering Manager or reports to Production Supervisor. Performs routine set up, operation, minor and major routine maintenance, preventative maintenance (PM) and troubleshooting of highly complex/auto...
Job Summary: A leading organization is seeking an experienced Validation Engineer to support validation strategy, compliance, and qualification activities for digital solutions in a GMP-regulated environment. Roles and Responsibilities: ...