A leading technology manufacturing company seeks a Test Engineer 1 in Warwick, RI. The role focuses on ensuring product quality through rigorous testing and validation processes. The ideal candidate holds a degree in Engineering and has a basic understanding of testing methodologies. Responsibilitie
Position Summary The Validation Manager is responsible for leading validation strategy, execution, and lifecycle management for pharmaceutical or biotech manufacturing systems, with a strong focus on sterile processes. This role requires hands-on expertise in protocol authorship (IQ/OQ/PQ), project
Title : Manufacturing Validation Engineer Openings: 1 Duration: 12‑month contract (rolling), expected 4-5yr min total duration Hourly Pay : Starting at $50/hr Location: Raynham, MA 02767 5 days per week onsite Target Start : 6/1 Interview Process : 2 rounds Must‑Haves Bachelor of Science in Manufact
NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates. Job Title : Project Lead - Validation (Supervisor) FLSA Classification : Full-Time, Exempt/Salary Professional Work Locat
Overview The Intern will assist validation department with routine validation tasks to include: Temperature Controlled Unit Mapping utilizing a validator and other data capture equipment, General report writing and generation of system database and list for qualified systems. Temperature mapping is
Validation Engineer Apex Systems is hiring for a Validation Engineer to work for one of our top Medical Device clients. Job: Validation Engineer Type: 18 month contract Location: Raynham, MA Requirements/Responsibilities: Minimum of B.S. In Engineering 3 + yrs. of experience in Med Device (Ortho pre
Job Title: Project Lead - Validation (Supervisor) Full-Time Work Location: Fall River, MA Work Hours: General Shift: 8:30AM – 5:00PM (May very based on business needs) Duties and Responsibilities: • Design, review and approve protocols for equipment and processes to produce pharmaceutical drug produ
This role is responsible for supporting base business operations and smaller-scale projects while driving process changes and continuous improvement initiatives. The position focuses on reducing scrap, optimizing manufacturing efficiency, and managing non-conformance investigations by implementing e
Summary: Supports testing and validation activities for medical devices, ensuring compliance with regulatory and quality standards. bility to interpret engineering drawings and specifications. Roles & Responsibilities: Develop Test Protocols aligned with design verification plans and regulatory
Overview The Intern will assist validation department with routine validation tasks to include: Temperature Controlled Unit Mapping utilizing a validator and other data capture equipment, General report writing and generation of system database and list for qualified systems. Temperature mapping is
1 weeks ago
Estimated salary for Validation in Warwick
$40,000 – $63,000/year
Estimation confidence: Low
Estimate based on market data for Warwick. Actual salaries may vary depending on experience, company, and area.