valid

About Made Scientific Made Scientific is a leading US-based cell therapy contract development and manufacturing organization (CDMO) specializing in the development, manufacturing, and release of autologous and allogeneic cell therapy products for clinical-and-commercial supply. Made Scientific combines the agility and entrepreneurial spirit of a specialist...

Job Summary: The Validation Lead is responsible for leading and supporting validation activities for GxP-regulated computerized systems across multiple client projects, including new implementations, system enhancements, and ongoing maintenance. This role collaborates with client stakeholders, vendors, and cross-functional teams to ensure systems comply...

Quality Assurance Analyst, Software ValidationAll the relevant skills, qualifications and experience that a successful applicant will need are listed in the following description. Chicago, IL area (Hybrid) | Regulatory Affairs / Quality AssuranceAbout the RoleOur client, a global manufacturer in the medical device and in-vitro diagnostics (IVD) space, is...

EQVAL Group, Inc. is a company that provides services to the manufacturing industry (Medical Devices, Pharmaceuticals, Biotechnologies, others). We work with an extraordinary group of professionals (employees and contractors) to accomplish the requirements established by our customers, in order to perform and provide a highly effective service.We are...

Job DescriptionChange the world. Love your job.Texas Instruments is seeking an Engineer - Validation to join our Analog Power Products organization in Dallas. Depending on your background and the needs of the team, you will be placed into one of three functions: product engineering, test engineering, or validation engineering.Responsibilities include: ...

About Us: BW Design Group is a fully integrated architecture, engineering, construction, system integration, and consulting firm committed to helping our clients realize their most critical goals from Strategy to Commercialization. As the only firm born from a manufacturing technology company to become an independent and fully integrated firm, we combine...

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life-threatening diseases. Headquartered in Bridgewater, New Jersey, we are advancing the next generation of cell therapy through a portfolio of innovative technologies, including autologous, allogeneic, and in vivo cell therapy approaches. Our research spans chimeric...

AI/ML Model Validation Specialist Location: Des Plaines; HYBRID (3 days onsite) Overview This role leads independent validation and governance of models across the enterprise — spanning AI systems, machine learning, and traditional statistical models — ensuring they meet regulatory standards and internal policy. Coverage areas include credit risk,...

COLSA is seeking a Certified RMF Validator to join our team and play a critical role in supporting cybersecurity and Risk Management Framework (RMF) activities . This position will provide expertise throughout the validation process, assessing security controls, documenting assessment results, and ensuring validation activities are performed in accordance...

Summary : We are seeking an experienced Process Validation Engineer to lead validation strategy, execution, and documentation. The role provides technical leadership across manufacturing, development, quality, and project teams within a cGMP environment. Roles & Responsibilities : • Develop and implement process validation,...

Job Summary: The Validation Lead is responsible for leading and supporting validation activities for GxP-regulated computerized systems across multiple client projects, including new implementations, system enhancements, and ongoing maintenance. This role collaborates with client stakeholders, vendors, and cross-functional teams to ensure systems comply...

Job Summary: The Validation Lead is responsible for leading and supporting validation activities for GxP-regulated computerized systems across multiple client projects, including new implementations, system enhancements, and ongoing maintenance. This role collaborates with client stakeholders, vendors, and cross-functional teams to ensure systems comply...

Validation Engineer Requirements: Hands-on experience with APS, EMPQ, and cGMP validation Experience with facility expansions/reconfigurations Experience introducing and validating isolator technologies Strong aseptic manufacturing background; Cell Therapy experience highly preferred

Job Title: Equipment Validation Engineer III Location: Bedford, Ohio Job Type: Full-Time Req ID: 11964 Summary The Equipment Validation Engineer III plays a key role in supporting a sterile pharmaceutical manufacturing facility through the qualification and lifecycle management of manufacturing equipment, utilities, and associated systems. This position...

Current job opportunities are posted here as they become available. Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management,...

WE’RE HIRING | OPPORTUNITY IN THE USA Validation & IT Engineer Pharmaceutical & Life Sciences Industry Quality Engineering is expanding its operations in the United States and is seeking a professional with experience in Validation, IT, and regulated environments* to support pharmaceutical and life sciences projects. You will work directly with client...

Job Summary: The Validation Lead is responsible for leading and supporting validation activities for GxP-regulated computerized systems across multiple client projects, including new implementations, system enhancements, and ongoing maintenance. This role collaborates with client stakeholders, vendors, and cross-functional teams to ensure systems comply...

Job Description & Skill Requirement: The Validation Engineer will support hardware validation activities, including motherboard rework, new hardware bring-up, lab inventory management, and procurement/shipping activities. Key Responsibilities: Perform hardware rework on Client motherboards, including: Resistors and capacitors Wiring and...

About Made Scientific Made Scientific is a leading US-based cell therapy contract development and manufacturing organization (CDMO) specializing in the development, manufacturing, and release of autologous and allogeneic cell therapy products for clinical-and-commercial supply. Made Scientific combines the agility and entrepreneurial spirit of a specialist...

A pharmaceutical manufacturing company is seeking a Validation Specialist to support a multi-year project portfolio at its site in the Clayton, NC area. This is a 24 month contract with potential to extend. Each specialist will lead validation on several projects at once, matched to their background in areas such as aseptic filling, device assembly and...