Medical Device Equipment Validator

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...

Job Description CSV specialist to perform validation activities on software and manufacturing equipment in a medical device industry.Skills: Computer system validation life cycle.Knowledge and experience validating software and medical devices equipment.Technical writing (English).Requirements Bachelor in Science 5 years of experience Experience in the...

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...

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...

Advantmed is hiring enthusiastic Medical Records TechniciansThis is a great "foot-in-the-door" position for those looking to be involved in the emerging Healthcare & Technology industry.  At Advantmed, our mission is to improve the healthcare system by ensuring appropriate, quality care, and eliminating unnecessary costs.Advantmed is a privately held...

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...

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...

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...

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...

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...

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...

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...

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...

At IPS, we're all about exceptional service and exceptional people.We're looking for a passionate In-Shop Technician who loves hands-on work, takes pride in their craft, and wants to have a meaningful impact.As an In-Shop Technician, every day will be different.You'll get to apply your knowledge and skills to solve complex problems and help critical...

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...

Overview of ResponsibilitiesThe Quality Assurance Manager will be responsible for ensuring compliance with FDA, ISO, and internal quality systems regulations.This includes reviewing plant defect reports, customer complaints, failure investigations, and audit findings to assess manufacturing-related issues that may impact quality.The manager will also conduct...

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...