Experienced GMP and Validation Specialist

About the Job:We are seeking an experienced CQV Turnover Engineer to join our team at Optimus Life Sciences. The successful candidate will have a university degree in pharmaceutical engineering, biotechnology or process engineering or a comparable subject, or several years of professional experience in the field of commissioning/qualification/validation...

Position Overview:This is an excellent opportunity to join Optimus Life Sciences as a CQV Turnover Engineer. As a key member of our team, you will be responsible for ensuring the commissioning and qualification of various process and utility systems, maintaining GMP compliance, and supporting other departments in preparing and implementing machine acceptance...

Key ResponsibilitiesIn this role, you will be responsible for:CQV activities: Carrying out hands-on CQV activities post-documentation phase, commissioning of process equipment, and ensuring GMP compliance.Process commissioning: Executing the commissioning of various process & utilities including upstream and downstream processes/utilities and clean and black...

Pharmatec Srl seeks a 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 the quality and integrity of our Clean and/or Black Utilities systems.Job Description:In this role, you will lead and execute Commissioning, Qualification, and Validation...

We are seeking a Senior QA Specialist to join our QA team in Copenhagen and contribute to the success of our outsourced GMP projects.This individual will be responsible for driving quality oversight for development projects and collaborating with global teams to ensure compliance with regulatory guidelines.The successful candidate will have a relevant...

We are seeking an experienced Clean Utilities Specialist to join our team at Pharmatec Srl in Copenhagen, Denmark. This role offers a unique opportunity to work on high-impact projects within the Life Sciences industry.Job Summary:The successful candidate will lead and execute Commissioning, Qualification, and Validation (CQV) activities for Clean and/or...

About the Role:At Agreena, we are seeking a detail-oriented Geospatial Data Validation Specialist to join our dynamic team. As a key member of the Programme Data Team, you will play a crucial role in validating farm field boundaries and agricultural data.Main Responsibilities:Boundary validationData input managementData reconciliationQuality controlReporting...

At Thor Companies, we are seeking a skilled Manufacturing Process Specialist to support our manufacturing, process optimization, and regulatory compliance projects across Denmark.The ideal candidate will have a strong background in the medical or pharmaceutical industry and be able to develop and optimize production processes for medical devices,...

As a QC Method Validation Expert, you will play a critical role in ensuring the accuracy and reliability of our analytical methods. You will work closely with our cross-functional teams to develop and implement methods that meet regulatory requirements, participate in operational planning, and ensure all activities follow cGMP guidelines.The QC Department is...

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...

Are you passionate about ensuring the quality and integrity of biopharmaceutical products? Do you have a strong background in analytical method development and validation?We are looking for a highly skilled Senior Bioassay Specialist to join our QC General Analytics team at AGC Biologics. In this role, you will be responsible for developing and implementing...

Job DescriptionWe are seeking a highly motivated and solution-oriented individual to join our Supply Chain QA team as a Warehouse Quality Assurance Specialist.The successful candidate will be responsible for ensuring the right quality level at Novo Nordisk external warehouses, setting direction in relation to requirement mapping, and implementing new...

A Process Control Specialist is needed to develop and maintain reporting tools to ensure project scope, cost, and schedule remain on track for a leading biotech company. This onsite role requires a strong background in automation, MES, PI data historian, and Infobatch systems within the pharmaceutical or biotech sector.Main Objectives:Manage the delivery of...

About the PositionThe company is seeking an experienced and skilled Ceramics Specialist to develop and upscale ceramic processes and products for solid oxide electrolyzer cells. The primary technical objective is to obtain fired structures defined by electrochemical feedback.Work will include both specifications for and commissioning of new equipment,...

Sr. IT Specialist - Cement IndustryWe are seeking an experienced Sr. IT Specialist to join our team, specializing in the cement industry. As a Sr. IT Specialist, you will be responsible for designing, developing, and maintaining software applications that optimize industrial processes for efficiency, stability, and sustainability.Key responsibilities will...

We are looking for an experienced Upstream Process Development Specialist to join our Clinical Team in Manufacturing Product Support department. As a key member of our team, you will be responsible for developing and implementing upstream processes for clinical products, ensuring compliance with GMP regulations.The ideal candidate has experience working in a...

We're looking for a skilled Process Improvement Specialist to join our team at Hamlyn Williams for a 12-month contract. This is an exciting opportunity to work on large-scale automation projects within the pharmaceutical or biotech sector.Responsibilities:Deliver high-quality process improvements that meet client expectationsCollaborate with vendors and...

About the RoleWe are looking for a highly motivated and experienced QA Process Specialist to join our team at Lundbeck A/S, H. In this role, you will play a key part in influencing the way we work with compliance and quality in our organization.Your Key ResponsibilitiesGlobal Training Development: You will develop and implement global training programs for...

Job DescriptionWe are seeking a skilled CQV Turnover Engineer to join our team at Optimus Life Sciences in Copenhagen, Denmark. As a mid-senior level professional, you will be responsible for carrying out hands-on CQV activities post-documentation phase, commissioning process & utilities, and ensuring GMP compliance.Your responsibilities will...

About the Role">As a key member of our Engine Platform Process Development team, you will play a crucial role in ensuring compliance with current and future IMO legislations.We are looking for an experienced specialist to join our cross-departmental team responsible for certification tasks. You will take on a lead role contributing to these efforts, shaping...