Validation Lead

About the Role">We are seeking a highly skilled IT Validation Lead to join our team in Facility & Equipment Validation at AGC Biologics. The successful candidate will be responsible for performing computerized qualification tests and protocols, compiling data and completing validation reports for implementation of new software. ">

In this role, you will be responsible for shaping the validation/qualification direction for computerized software at AGC Biologics. As Senior IT Validation Scientist, you will oversee the entire validation process, ensuring that all activities meet the highest standards of quality and compliance.">Your Key ResponsibilitiesDevelop and execute comprehensive...

AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. Our mission is to bring life-changing therapies for patients around the globe.We are currently...

About the RoleWe are seeking a highly skilled IT minded validation expert to join our Facility & Equipment Validation department.Responsibilities:Responsible for performing qualification tests and protocols, compiling data and completing validation reports.Leading the different validation activities from planning, execution to completion.Ensuring current...

AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners.Our mission is to work together with our customers to improve patients' lives by bringing new biopharmaceuticals to...

The Ubique Systems' IT Compliance Lead plays a crucial role in ensuring the Genetics Analysis Platform meets regulatory requirements. The platform is a Non-GxP SaaS solution, and the IT Compliance Lead will develop and execute a validation strategy.Responsibilities include creating end-to-end documentation, performing assessments, and writing reports. The...

Genmab is an international biotechnology company committed to developing innovative antibody therapeutics that transform patient care. We are dedicated to creating next-generation antibody technology platforms and leveraging translational research and data sciences to push the boundaries of what is possible.About Our MissionWe strive to make a meaningful...

AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities across three continents.About the Team:The QC Chemistry Department is responsible for...

As a leading technology consulting firm, Amaris Consulting delivers innovative solutions to businesses worldwide. We're looking for a skilled consultant with expertise in railway safety systems to join our team.About the RoleThis key position will focus on system integration, configuration, and validation of trackside components, ensuring compliance with...

Hamlyn Williams is a leading consulting firm in the pharmaceutical industry. As a Validation Engineer with our client, you will be responsible for ensuring the quality and safety of their products.The ideal candidate will have experience with SDLC methodologies and strong knowledge of steam sterilizers, autoclaves, lyophilizers, depyrogenation tunnels, smoke...

We are seeking a highly skilled Validation Engineer to join our team at Hamlyn Williams. As a Validation Expert for the pharmaceutical industry, you will play a critical role in ensuring the quality and safety of our clients' products.Your key responsibilities will include validating equipment and processes to ensure compliance with regulatory requirements,...

Senior IT Validation Scientist page is loaded Senior IT Validation Scientist Apply locations Copenhagen, Denmark time type Full time posted on Posted 30+ Days Ago job requisition id JR101494 Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow. Our mission is to work...

Senior IT Validation Scientist page is loadedSenior IT Validation ScientistApply locations Copenhagen, Denmark time type Full time posted on Posted 30+ Days Ago job requisition id JR101494Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow. Our mission is to work...

As a Senior Validation Engineer, you will play a critical role in the development of clean and black utilities systems at Pharmatec Srl.Senior Validation Engineer – UtilitiesYou will lead and execute commissioning, qualification, and validation activities, develop and review CQV documentation, and collaborate with cross-functional teams to ensure...

As a key member of the Ubique Systems' team, the IT Compliance Lead will be responsible for defining and executing a validation strategy for the Genetics Analysis Platform. This Non-GxP SaaS solution requires close attention to ensure compliance with internal and external regulatory requirements.The role involves delivering end-to-end documentation,...

Hiring Manager: Hamlyn Williams We are a leading consulting firm in the pharmaceutical industry, specializing in recruitment and staffing solutions for the life sciences sector. We help our clients find the best talent for their teams, and we're now looking for a talented Validation Engineer to join our network.The ideal candidate will have experience with...

Role OverviewThis position plays a crucial role in ensuring the quality and compliance of our computerized systems.Duties and Responsibilities:Performing qualification tests and protocols for new software implementation.Leading the validation process from planning to completion.Ensuring data integrity through accurate record-keeping and...

About Our TeamLocal Manufacturing - Projects and Site Support is a dynamic team within Novo Nordisk A/S, responsible for establishing and operating local manufacturing sites globally. We strive to raise the quality and performance level at our local sites, working together to achieve this goal.In this role, you will be part of a talented team of specialists,...

Greatercph is a leading Contract Development and Manufacturing Organization (CDMO) specializing in the development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells.">About the TeamYou will join a highly experienced team of professionals who share...

Hamlyn Williams is seeking an experienced E&I Engineer to join our team in Denmark.E&I Specialist Consultant | Validation EngineeringThe successful candidate will have a strong background in automation and validation engineering, with experience working on large-scale pharmaceutical projects.Key Responsibilities:Liaising with vendors to ensure smooth project...