MV01-101325 Manufacturing Engineer / Validation Specialist - Dorado,

Validation Specialist with experience in regulated industry validating/qualifying laboratory equipment manufacturing equipment processes utilities and facilities. · ...

Validating laboratory equipment manufacturing equipment processes utilities and facilities. · ...

Sr. Validation Specialist with experience in automated equipment and vision system validation. · ...

+Job summary · A Validation Specialist ensures manufacturing equipment, utilities, software, and processes consistently produce products meeting regulatory (FDA/EMA) and company quality standards. · +ResponsibilitiesDraft, review, and execute Validation Master Plans. · ...

This is a validation specialist position with hands-on experience in executing validation and qualification activities across diverse areas. · ', ...

We are seeking a detail-oriented Manufacturing Engineer / Validation Specialist to join our team. The ideal candidate will be responsible for designing, implementing, and maintaining manufacturing processes in compliance with regulatory standards. · Bachelor's degree in Engineeri ...

This job is for a Validation Engineer to provide support to qualification/validation activities related to manufacturing equipment. · ...

Responsibilities: · The Cleaning Validation Specialist (Contractor) will support the introduction of new products in a Contract Manufacturing Organization (CMO) environment. · This role is responsible for developing and executing the full cleaning validation lifecycle, including: ...

· Education: Engineer, Science Related.  IE Prefered · Years of Experience: 3-5 · Skills: · Statiscal data Analyst and · Six Sigma Green Belt Certified - Prefered · Knolwlwdge in Validations Strategies Development and Implementations · Product Tranfers · Computer Validation L ...

· Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutic ...

· For Packaging services in the Engineering area · WHAT MAKES YOU A FIT:  · The Technical Part: · Bachelor's Degree in Engineering with five (5) years of Engineering experience within the pharmaceutical or medical device industry. · Bilingual (English & Spanish). · Project Manag ...

· For Process Validation services in the manufacturing area.  · WHAT MAKES YOU A FIT:  · The Technical Part: · Bachelor's in Life Science or Engineering with five (5) years of experience in Process Validation activities within the Pharmaceutical Industry.   · Excellent written a ...

This resource will attend all related meetings making required documents corrections and changes following up on document revision and approval. · ...

This resource will attend all related meetings, making required documents corrections and changes and following up on document revision and approval. · ...

· Company Description · Validation & Engineering Group provides world-class service and expertise to the Biotechnology, Pharmaceutical, Medical Devices, Chemicals (API), Food, and Cosmetics industries.  For over twenty years, V&EG has placed the most talented individuals in a po ...

Seeking Process Validation Specialist with experience in ethylene oxide (ETO) sterilization processes to ensure process effectiveness and safety for medical or industrial products. · ...

Process validation specialist with experience in ethylene oxide sterilization processes to guarantee effectiveness and safety for medical or industrial products. · Develop IQ/OQ/PQ validation protocols for EtO sterilization processes. · Conduct load configuration studies, gas pen ...

The Cleaning Validation Specialist leads and executes risk-based cleaning validation and verification activities across manufacturing operations, ensuring compliant strategies for equipment cleaning, residue removal, and lifecycle management aligned with current GMP and global he ...

· Validation Specialist — Equipment  · Location: Barceloneta, Puerto Rico (On-site) · Shift: Day (8:00 a.m. – 5:00 p.m.) · Start: ASAP · Role Overview · Execute and support validation for new and existing equipment, partnering closely with Construction, Utilities, Operations, an ...

Process validation specialist with experience in ethylene oxide sterilization processes. · ...