Technical Validation Engineer

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...

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...

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...

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 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...

Job Description: Minimum of 5 Yr exp leading the validation of a major capital automation projects.1.Validation and Compliance Knowledge GxP (Good Practice) Guidelines: Familiarity with GxP guidelines such as Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and Good Clinical Practice (GCP).FDA 21 CFR Part 11: Understanding of the regulatory...

**Job Description**Lumiere Systems is seeking a highly skilled Validation Documentation Specialist to join our team. This role will be responsible for managing document trackers, creating FAT & SAT documentation, and supporting the execution of IQ, OQ & PQ testing.The ideal candidate will have strong written and verbal communication skills, as well as...

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...

At Qrc Group Llc, we are seeking a highly skilled Data Validation Specialist to join our team. This role will be responsible for performing validation activities on software and manufacturing equipment in the medical device industry.Skill Requirements:Computer system validation life cycleKnowledge and experience validating software and medical devices...

Aseptic Process Engineer/Lead to design and support the aseptic manufacturing processes at designated locations. Responsible for supporting the planning, execution, tracking, and completion of key aseptic related projects such as but not limited to: Production process/systems implementation, shut down/restart process, media fill oversight, deviation...

Process Engineer to analyze, design, and optimize manufacturing and production processes. Will be responsible for improving efficiency, ensuring product quality, and driving continuous improvement initiatives.Provide direct support to the manufacturing team and collaborates with the automation engineer to produce a streamline automated manufacturing...

Process Engineer to analyze, design, and optimize manufacturing and production processes. Will be responsible for improving efficiency, ensuring product quality, and driving continuous improvement initiatives.Provide direct support to the manufacturing team and collaborates with the automation engineer to produce a streamline automated manufacturing...

Lumiere Systems is a forward-thinking company that requires a Senior Validation and Compliance Professional to lead our validation efforts. As a key member of our team, you will be responsible for the validation of major capital automation projects. With a minimum of 5 years' experience in leading validation efforts for large-scale automation projects, you...

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...

At Lumiere Systems, we are seeking an experienced Data Validation and Automation Specialist to lead the validation of major capital automation projects. This role requires a minimum of 5 years' experience in leading validation efforts for large-scale automation projects.Key Responsibilities:1. Validation and Compliance Knowledge: The ideal candidate will...

Aseptic Process Engineer/Lead to design and support the aseptic manufacturing processes at designated locations. Responsible for supporting the planning, execution, tracking, and completion of key aseptic related projects such as but not limited to: Production process/systems implementation, shut down/restart process, media fill oversight, deviation...

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 (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...

About Our TeamWe are a world leader in life science engineering and technical solutions, providing comprehensive portfolios of technical support and solutions for the FDA-regulated industry.Our team is dedicated to ensuring compliance with FDA, ISO, and internal quality systems regulations.We have offices in various locations, serving clients in six global...

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...