CSS Senior Technician
in sample management. OR HS Diploma + 4 years demonstrated proficiency in sample management. Life Science Degree, preferred...
in sample management. OR HS Diploma + 4 years demonstrated proficiency in sample management. Life Science Degree, preferred...
Roles & Responsibilities: Play a client facing Compliance Lead role in projects, programs, and support work. Provide consulting and guidance on quality and compliance needs to IT project teams and enable them to achieve compliance using ...
Summary: Supports testing and validation activities for medical devices, ensuring compliance with regulatory and quality standards. Ability to interpret engineering drawings and specifications. Roles & Responsibilities: Develop Test P...
Responsibilities: Provide Quality Engineering support for commercial medical device products. Develop, modify, apply and maintain quality standards and protocol for processing materials into partially finished or finished materials produ...
Job Description: We are seeking a Product Development Tech for our Brea, CA facility. This person contributes to the completion of routine technical tasks and develops solutions to routine technical problems of specified scope. Their conta...
Job Description: In this role as a Production Technician, you will be responsible for leading a production team and/or participating in a specific team or assignment. Duties may include working on a semi-automated machine line, handling ma...
Summary: We are seeking a proactive and detail-oriented NPI Project Engineer to lead the end-to-end execution of small to medium, cross-functional product development projects—from early concept through design, prototyping, and production ...
Summary : We are seeking a Techno-Functional Specialist with strong expertise in Labware LIMS Development with GxP-compliant process awareness and hands-on experience in ServiceNow. The ideal candidate will bridge the gap between technolog...
standards (e.g., ICH-GCP, CDISC) Requirements: Bachelor's degree in a life science, health science, pharmacy, public health...
Job summary: 5+years of CQV experience focused on utilities, process equipment, and process validation. Strong documentation experience across CQV lifecycle deliverables including URS/FRS, risk assessments, protocols, summary repor...