GMP Validation Professional

GMP Compliance Engineer PositionOptimus Life Sciences seeks a skilled GMP Compliance Engineer to join our team in Copenhagen, Denmark. As a key member of our engineering team, you will be responsible for maintaining GMP compliance for the engineering department.About the Role:This role involves ensuring that all commissioning procedures are completed to...

Validation and Commissioning Expert WantedOptimus Life Sciences seeks a highly skilled Validation and Commissioning Expert to join our team in Copenhagen, Denmark. As a key member of our engineering team, you will be responsible for ensuring GMP compliance for the engineering department.About the Role:This role involves developing and implementing effective...

We are looking for a highly motivated and experienced QA professional to join our team as an Advanced QA Professional. The ideal candidate will possess a strong understanding of GMP regulations and quality assurance principles, as well as excellent communication and interpersonal skills.The successful candidate will be responsible for ensuring best-in-class...

As a Senior IT Validation Scientist at AGC Biologics, you will play a critical role in ensuring the quality and compliance of our computerized systems. Your expertise in validation and qualification will enable us to maintain the highest standards of quality and regulatory compliance.">Your Skills and QualificationsA degree in a relevant field, such as...

As a Process Specialist at European Tech Recruit, you'll be responsible for designing, specifying, and overseeing the installation of new process equipment. You'll provide technical support and troubleshooting for Upstream (Cell Culture), Downstream (Purification), Clean Utility/CIP, and Solution Preparation systems.About the Job FunctionThe ideal candidate...

Job DescriptionAs a Validation and Packing Process Specialist, you will play a central role in setting direction for our local production sites. Your process experience e.g. within tablets, assembly or packaging of prefilled devices will have a significant impact and will be instrumental in setting direction and shaping our everyday work and support to our...

Job SummaryThis is a unique opportunity to shape the validation direction for computerized software in AGC Biologics.Main Responsibilities:Driving validation activities end-to-end for computerized software.Collaborating with the team to ensure compliance with GMP/IT/validation requirements.Developing and implementing efficient validation...

About the Role:We are seeking an experienced Analytical Specialist to join our GMP laboratory. The successful candidate will be responsible for ensuring the quality of analytical procedures for new injectable drug products.The role involves supporting chemical analysis of injectable drug products, both internally in the department and globally in QC...

About the RoleWe are seeking a highly skilled GMP Compliance Specialist to join our team at Novo Nordisk A/S. As a Senior Quality Assurance Leader, you will play a critical role in ensuring adherence to Good Manufacturing Practice (GMP) compliance requirements and best practices across all operations in Local Manufacturing.In this position, you will provide...

About This OpportunityWe are looking for a Production and Process Specialist who can make a meaningful contribution to our team's mission. As a key player, you will be instrumental in shaping our local manufacturing operations, driving process improvements, and ensuring high-quality standards.In this role, you will have the opportunity to:Work closely with...

Select how often (in days) to receive an alert: Create AlertLocation:Bagsværd, Capital Region of Denmark, DKWould you like to be part of one of Novo Nordisk's expansion projects to increase our API capacity for clinical trials, enabling us to serve more people living with serious chronic diseases globally? Are you motivated by joining a rapidly growing...

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...

Lundbeck A/S, H is a global leader in the discovery and development of innovative treatments for brain disorders. We are committed to transforming lives by addressing the big unmet needs of people living with brain disorders.We are seeking a GMP Quality Assurance Professional - Biologics Manufacturing to join our team in Copenhagen, Denmark. As a member of...

Select how often (in days) to receive an alert: Create Alert Would you like to take the next exciting step in your career by playing a key role in a dynamic and impactful business support unit, driving meaningful change in Local Manufacturing production? Does using your hands-on expertise in deviation handling and cGMP to tackle tasks, enhance processes, and...

Passionate about Quality Assurance with expertise within outsourced GMP activities and development projects? Ascendis Pharma invites you to explore the role of our newest QA Specialist / QA Professional for Development GMP activities. With roots spanning Denmark, Germany, and the United States, Ascendis Pharma A/S emerges as an innovative and dynamic...

Job Overview:This Quality Assurance and Control Professional role is responsible for ensuring the quality of analytical procedures for new injectable drug products. The successful candidate will work closely with our analytical chemists to ensure that our analytical methods are scientifically sound and fit for purpose.The position requires a Ph.D. in a...

About LundbeckLundbeck A/S, H is a leading global pharmaceutical company that specializes in the development and production of innovative treatments for brain disorders. Our team is passionate about making a difference in the lives of those affected by neurological and psychiatric disorders.The role you are applying for is a critical part of our efforts to...

Passionate about Quality Assurance with expertise within outsourced GMP activities and development projects?Ascendis Pharma invites you to explore the role of our newest QA Specialist / QA Professional for Development GMP activities.With roots spanning Denmark, Germany, and the United States, Ascendis Pharma A/S emerges as an innovative and dynamic...

Key Responsibilities:As a Regulatory Compliance Expert in our QC General Analytics team, you will be responsible for ensuring all activities follow cGMP and participating in analytical method validations. You will also participate in operational planning together with your colleagues and support regulatory inspections and customer audits.The successful...

Do you have the courage for a steep learning curve in Novo Nordisk, both professionally and personally in collaboration with a strong team? Are you ready to take on responsibility for keeping our operational equipment running? If yes – and you can imagine yourself as our new pilot scientist – this is the job for you Apply today and join us for a...