Engineering Validation Expert

Mentor Technical Group is an equal opportunity employer, committed to providing a comprehensive portfolio of technical support and solutions for the FDA-regulated industry.Job Description:Design and develop validation protocols for serialization equipment, processes, and systems.Collaborate with cross-functional teams to ensure the integrity and quality of...

We are looking for an Engineering Validation Expert - CSV to join our team at Lumiere Systems. In this role, you will be responsible for leading the validation of major capital automation projects. With a minimum of 5 years' experience in leading validation efforts for large-scale automation projects, you will bring expertise in the following areas:Key...

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 in...

Mentor Technical Group provides comprehensive technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering, we have the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines.Job Summary: We are seeking a meticulous and experienced...

Company OverviewThe Qrc Group Llc is a leading organization in the medical device industry, dedicated to providing innovative solutions and ensuring the highest standards of quality.Job SummaryWe are seeking a skilled CSV specialist to perform validation activities on software and manufacturing equipment. The ideal candidate will have a strong background in...

Job DescriptionWe are seeking a skilled Cybersecurity Engineer to join our team in Colombia. The ideal candidate will have a strong background in Information Security and be able to design, implement, and maintain secure systems.The successful candidate will be responsible for:Defining and establishing accreditation and validation strategies from an...

Skills: Capital Automation Projects, GxP, GMP, GLP, GCP, FDA, ISO, OQ, PQ, CSV, SCADA, SAP Job Description: Responsibilities Management of document tracker (Actively updating the document Listing of all documents for review | approval).This includes following up with reviewers / approvers, to ensure documents are reviewed / approved on time.FAT & SAT...

We are looking for a Medical Device CSV Expert to perform validation activities on software and manufacturing equipment in our medical device industry.About Us:Qrc Group Llc is a leading company in the medical device industry, dedicated to delivering high-quality products and services.Job Description:Validate software and manufacturing equipmentDevelop and...

We are seeking an experienced validation specialist to join our team at Mentor Technical Group. Our company provides technical support and solutions for the FDA-regulated industry, ensuring compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines.Job Requirements:Bachelor's degree in Engineering, Computer Science, or a...

At Qrc Group, Llc, we are seeking an experienced Regulatory Consultant to provide expert guidance and support in navigating the regulatory landscape of aseptic production environments.Key Responsibilities:Provide expert regulatory advice for aseptic manufacturing processes, ensuring compliance with FDA and global regulatory standards.Prepare and review...

Job Description Project Manager to lead and manage projects in the aseptic areas, particularly in the development, validation, and FDA submission processes for pharmaceutical and medical device products.Responsibilities: Develop project timelines, resource allocation plans, and budgets, ensuring timely and on-budget delivery.Coordinate and oversee all stages...

**Role Overview:**We are seeking a highly skilled Quantitative Business Expert to join our team at Buscojobs Puerto Rico. As a key member of our analytics department, you will play a critical role in driving business decisions with data-driven insights.About the Position:Develop and implement complex statistical, financial, and accounting models for...

Medical Devices Industry ExpertiseThe ideal candidate will have a strong background in the medical devices industry, with a minimum of 5 years of experience. They will also have a bachelor's degree in a relevant field, such as science or engineering.Computer System ValidationThe CSV specialist will be responsible for performing validation activities on...

Project Manager to lead and manage projects in the aseptic areas, particularly in the development, validation, and FDA submission processes for pharmaceutical and medical device products.Responsibilities:Develop project timelines, resource allocation plans, and budgets, ensuring timely and on-budget delivery.Coordinate and oversee all stages of project...

**Job Summary:**We are seeking an experienced Product Manager to join our Digital Banking and Payments Team. As a Product Owner, you will be responsible for articulating and understanding the product vision, leading roadmap definition, and guiding cross-functional teams.**Key Responsibilities:*Develop and communicate a clear product vision and strategy that...

Job DescriptionWe are seeking an experienced Automation Engineer to join our team. The ideal candidate will have a strong background in manufacturing automation systems maintenance and be able to apply advanced engineering principles to design and implement major system modifications.

Job Description Regulatory Consultant will provide expert guidance and support in navigating the regulatory landscape, specifically in aseptic production environments.Responsibilities:  Provide expert regulatory advice for aseptic manufacturing processes, ensuring compliance with FDA and global regulatory standards.Prepare and review regulatory submissions...

Regulatory Consultant will provide expert guidance and support in navigating the regulatory landscape, specifically in aseptic production environments.Responsibilities: Provide expert regulatory advice for aseptic manufacturing processes, ensuring compliance with FDA and global regulatory standards.Prepare and review regulatory submissions to the FDA,...

**Job Description**We are seeking a highly skilled IT project manager to join our team at Smartlogix. The ideal candidate will have extensive experience in IT project management, with a strong understanding of agile and traditional project management methodologies.About the CompanySmartlogix is a leading organization in the industry, known for its innovative...

Qrc Group, Llc is seeking an experienced Regulatory Consultant to join our team as a subject matter expert in aseptic manufacturing regulations.Key Responsibilities:Develop and maintain deep knowledge of FDA regulations and industry standards for aseptic processing and pharmaceutical products.Collaborate with cross-functional teams to prepare and submit...