Technical Writer And Validation Support Engineer

**Job Summary**We are seeking a highly skilled Technical Validation Engineer to join our team at Lumiere Systems. In this role, you will be responsible for creating and maintaining validation documentation, including test plans, test scripts, and validation reports.You will also work closely with technical teams to understand and document requirements, as...

**About the Role**Lumiere Systems is looking for a talented Regulatory Compliance Writer to create high-quality documentation that meets regulatory requirements. As a Regulatory Compliance Writer, you will play a critical role in ensuring that our company's products meet the necessary standards and regulations.In this role, you will be responsible for...

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...

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...

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...

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**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...

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...

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...

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...

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...

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...

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...

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...

Company Overview Mentor Technical Group (MTG) provides a complete portfolio of technical support and solutions to the FDA-regulated industry.As a global leader in life sciences engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy...