Validation Specialist Jobs in Andover, MA

About Us: BW Design Group is a fully integrated architecture, engineering, construction, system integration, and consulting firm committed to helping our clients realize... Read More

We are seeking a highly experienced Senior CQV (Commissioning, Qualification, and Validation) Engineer to join our team. The ideal candidate will possess a robust... Read More

We are seeking a Quality Assurance Specialist to join our Quality Operations Team. In this role, you will support the lifecycle of GxP equipment, instruments, computer... Read More

Roles Responsibilities: Support the commissioning, qualification, and validation of facility equipment and control systems. Review and approve all associated documents,... Read More

We are seeking a Quality Assurance Specialist to join our Quality Operations Team. In this role, you will support the lifecycle of GxP equipment, instruments, computer... Read More

Title: Sr. Quality Engineer Location: Andover, MA Contract Term: 12+ Months Weekly 40.00 hours 1st Shift (8AM 5PM ) The Quality Engineer will work as a member of a... Read More

Responsibilities may include the following and other duties may be assigned. Develops, modifies, applies and maintains quality standards and protocol for processing... Read More

The Senior Quality Engineer is responsible for developing, improving and maintaining AVIs Quality Systems, and overseeing aspects of the quality control operations. This... Read More

Job Description Job Description This Senior Quality Engineer will support quality manufacturing initiatives for electronic components used in defense, aerospace and... Read More

By clicking the Apply button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be... Read More

Must Have: 2-5 Years Experience in Quality with BS in Engineering Process Validation and Computer software validation knowledge. Process Characterization, Process... Read More

Description Responsible for batch record review Assess CMO batch compliance with FDA and ICH regulations Support investigations and deviations Review and approve documents... Read More

By clicking the Apply button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be... Read More

Description Responsible for batch record review Assess CMO batch compliance with FDA and ICH regulations Support investigations and deviations Review and approve documents... Read More

As a validation strategist, you will lead the development and execution of compliant and nimble validation strategies for cloud based (SaaS, PaaS) clinical, regulatory,... Read More

About UFP MedTech: UFP Technologies is a designer and custom manufacturer of comprehensive solutions for medical devices, sterile packaging, and other highly engineered... Read More

Job Title: Senior Quality Assurance Start Date: ASAP Duration: 12 months Location: Andover, MA Hours per Week: 40 Position Overview: The QA Senior Associate plays a... Read More

Date Posted: 2024-10-22 Country: United States of America Location: MA113: Andover MA 352 Lowell Hampshir 352 Lowell Street Hampshire, Andover, MA, 01810 USA Position Role... Read More

Job Description Job Description Verista s 600 experts team up with the world s most recognizable brands in the life science industry to solve their business needs. The... Read More