Medical Device CSV Expert

Job DescriptionThe CSV specialist will be responsible for performing validation activities on software and manufacturing equipment in the medical device industry. This includes developing and maintaining technical documentation, collaborating with cross-functional teams, and ensuring compliance with industry regulations.Skills RequiredComputer system...

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...

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...

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 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...

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...

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...

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...

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...

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...

Optum's Commitment to Diversity and Inclusion">We believe that diversity and inclusion are essential to achieving our mission. We strive to create a workplace that reflects the diversity of the communities we serve, where everyone feels valued, respected, and empowered to contribute.We are committed to recruiting, retaining, and developing a diverse...

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 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...

Company OverviewMentor Technical Group (MTG) is a global leader in life sciences engineering and technical solutions, providing comprehensive support to the FDA-regulated industry. Our expertise ensures compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines.Job SummaryThis position is responsible for coordinating and...

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 (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...

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...