Empleos: technical author

For Validation services in the Manufacturing area.WHAT MAKES YOU A FIT: The Technical Part:Bachelor's Degree in Science or Engineering and (2) two years of experience within the Medical Devices Industry.Bilingual: Spanish and EnglishSoft Skills: Excellent leader skillsShift: Administrative, and according to business needs. Experience in: Test Method...

For Validation services in the Manufacturing area.WHAT MAKES YOU A FIT: The Technical Part:Bachelor's Degree in Science or Engineering and (2) two years of experience within the Medical Devices Industry.Bilingual: Spanish and EnglishSoft Skills: Excellent leader skillsShift: Administrative, and according to business needs. Experience in: Test Method...

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.Responsibilities:Supports equipment...

For Validation services in the Manufacturing area.WHAT MAKES YOU A FIT:The Technical Part:Bachelor's Degree in Science or Engineering and (2) two years of experience within the Medical Devices Industry.Bilingual: Spanish and EnglishSoft Skills: Excellent leader skillsShift: Administrative, and according to business needs.Experience in:Test Method Validation...

For Validation services in the Manufacturing area.WHAT MAKES YOU A FIT:The Technical Part: * Bachelor's Degree in Science or Engineering and (2) two years of experience within the Medical Devices Industry. * Bilingual: Spanish and English * Soft Skills: Excellent leader skills * Shift: Administrative, and according to business needs. * Experience in: * Test...

Under general supervision, the Senior Scientist conceives, designs, implements, and executes scientific experiments and technical strategies that support commercial biopharmaceutical manufacturing operations. This role contributes to the successful completion of projects through experimental design, data analysis, regulatory documentation, and direct...

Provide technical process engineering support for oral solid dose (OSD) formulation operations to ensure safe, compliant, and efficient manufacturing. Execute process monitoring, troubleshooting, and continuous improvement to enhance robustness, quality, and cost performance. Contribute to GMP readiness and audit resilience by maintaining strong...

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 pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices...

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 pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices...

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 pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices...

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 pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices...

SummaryWe are seeking a Process Development Scientist to conceive, design, implement, and execute scientific studies that support commercial biopharmaceutical manufacturing operations. This role contributes directly to formulation and aseptic filling processes, ensuring robust, compliant, and data-driven process performance.The selected candidate will work...

Job Title: Autoclave & Sterilization EngineerLocation: Onsite – Puerto Rico (Open for Puerto Rico Residents)Employment Type: Contract through ProQuality NetworkSchedule: Onsite role on administrative shift with flexibility to work shifts as neededPosition SummaryProQuality Network is seeking a highly skilled Autoclave & Sterilization Validation Specialist...

The Specialist Manufacturing supports the execution and continuous improvement of manufacturing and quality systems with minimal supervision. This role applies scientific, operational, and compliance knowledge to support manufacturing operations, including non-conformances, process validation, procedures, training, and new product introductions. The...

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals...

Job DescriptionABM is seeking a highly experienced and rapid-response Due Diligence Manager to manage the critical site assessment phase for the Waymo expansion portfolio. This strategic role is responsible for the preliminary technical, operational, and financial vetting of potential new sites (e.g., existing buildings, lease opportunities, or new...

Job DescriptionABM is seeking a highly experienced and rapid-response Due Diligence Manager to manage the critical site assessment phase for the Waymo expansion portfolio. This strategic role is responsible for the preliminary technical, operational, and financial vetting of potential new sites (e.g., existing buildings, lease opportunities, or new...

The Scientist is responsible for conceiving, designing, implementing, and executing scientific and engineering experiments that support project objectives under general supervision. This role contributes to the development of robust processes, generation of reliable data, and advancement of scientific and technical capabilities within a regulated...

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals...

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.We are seeking a talented, dedicated individual...