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- Fohntech group are seeking highly organized and detail-oriented QAQC Turnover Package Engineer to manage the compilation, coordination, and submission of turnover documentation for a pharmaceutical project. Key Responsibilities: · Ensure all documentation (including...
- ...responsibilities: Operate and maintain HVAC systems in compliance with GMP and ISO standards. Monitor and optimize airflow, temperature,... ...integrity. Collaborate with cross-functional teams including QA, maintenance, and production. Support validation,...
- ...Senior Validation Engineer Assembly Validation & GMP Team Hillerød, Denmark Would you like to be in the frontline of device... ...corporate teams, R&D, production units, suppliers, Quality Assurance (QA), and specialists, while gaining exposure to diverse projects and...
- ...Qualified Person in Device Manufacturing & New Product Introduction QA (DMN QA) and play a pivotal role in ensuring the quality and... ...upload your diploma. Have 5 or more years of experience within a GMP regulated manufacturer, preferably in quality assurance. Have...
- ...forandringsprocesser Har et personligt motiverende drive Naturlig sans for service og samarbejde. Det er en fordel, hvis du har GMP erfaring, ligesom du formentlig har erfaring med afvigelser, ændringssager og SOP’er. Vores arbejde må aldrig kompromittere...
- ...mainly physical tests. Your skills and qualifications We expect you to have: A relevant science degree Experience in GMP in laboratories, in a regulated laboratory environment. Full proficiency in in both Danish and English. You like to collaborate...
- ...ramping up new state-of-the-art sites to meet future demand. We’re committed to delivering the high-est quality APIs in compliance with GMP and continuously improving our processes and ways of working. Your skills & qualifications We’re looking for a new...
- ...technical backgrounds are a plus, though leadership capabilities are prioritized ~Experience managing deviations and familiarity with GMP principles or regulatory requirements for the pharmaceutical and medical devices industry ~Leadership experience, whether formal or...
- ...change management Experience working in highly complex, matrix environments, ideally in a manufacturing environment (preferably within GMP and manufacturing processes) Proven ability to navigate ambiguity, facilitate progress in operational transitions, and create...
- ...translating complex requirements into effective solutions. Collaborate closely with stakeholders across production, IT, automation, QA/QC, and external partners, maintaining project oversight and communicating clearly to align deliverables and strategy. Design for...
- ...experience of working cross functionally and building relations with stakeholders at all organisational levels. · Experience from a GMP regulated environment as well as aseptic or finished production areas will be considered an advantage. · Professional proficiency...
- ...demonstrate: A Master’s degree in Natural Sciences or a related field, with experience in Quality Assurance, Quality Control, or GMP-regulated production. At least five years of leadership experience, including proficiency in GMP regulations and management systems...
- ...position As a Validation Specialist, you will play a versatile role, collaborating with multiple stakeholders including line management, QA, process experts, test and validation engineers, and commercial device manufacturing. You will be instrumental in steering our...
- ...or highly regulated industries. - A solid leadership toolkit with demonstrated success. - Familiarity with LEAN methodologies and GMP knowledge is advantageous. As a sustainable employer, we encourage decisions and behaviours that support positive financial,...
- ...eller lignende Du har gode IT-kompetencer (Herunder Word og Excel), samt god forståelse for kvalitet og gerne et godt kendskab til GMP og cLEAN Erfaring med skiftehold er en fordel Erfaring med systemerne DeltaV, SAP og PAS-X eller lignende er en fordel Gode...
- ...mobile robotics e.g.: (Universal Robots, Kuka, MIR, Omron, Nipper). As documentation according to Good Manufacturing Practice (GMP), rules are part of our daily work, it is important that you thrive in ensuring that all your work is well documented. We also...
- ...improvement and supports your professional and personal development. Your new role Join our Global Contract Manufacturing Devices QA (GCM Devices QA) team at Novo Nordisk, where you'll have the unique opportunity to influence the quality of medical device components...
- ...instructions and working knowledge of FDA and EU regulations is preferred. ~+3 years of experience from a similar job or project with GMP responsibility within room conditions (HVAC, BMS, FMS). ~ Full professional proficiency in English. On a personal level you...
- QA Specialists Join our Talent Network Gi Group is an international staffing agency with more than 500 locations in 40 countries. QA talents are in high demand! - QA is a central part of many Life Science companies' daily functioning. At Gi Group, we want to...
- Senior QA Manager - Secomea ...
- ...growth as we scale our industrial B2B SaaS platform. About the Role: As we scale, quality is everything. We’re seeking a Senior QA Manager who can take a strategic, hands-on approach to quality assurance, ensuring both our software and hardware solutions meet the...
- ...værdi for vores kunder. Hos Mustache sætter vi en ære i at arbejde som et team, og ud over at lære hvordan vi arbejder med test og QA, vil du lære hvordan selve processen bag et udviklingsteam er sat op. Som praktikant vil du blive en del af vores kultur og opleve hvordan...
- ...GMP Packaging Specialist, Finished Goods Production Are you passionate about creating an environment where quality, compliance, and production efficiency go hand in hand? Do you have a solid understanding of GMP requirements and experience in Finished Goods Production...
- ...role In close cooperation with your colleagues, you act as a QA for QC servicing our internal and external QC laboratories. Novo... ...industry. Have solid and up-to date knowledge of quality and GMP requirements. Knowledge within analysis validation and working...
- ...forefront of digital transformation, ensuring a competitive edge in a rapidly evolving travel landscape The Job: The Automation QA Engineer role within Kuoni Tumlare, delivering testing across various projects and individual IT developments & applications. Working...
- ...protocols (IQ/OQ/PQ) and related documentation in alignment with GMP, GxP, and client-specific requirements * Execute temperature... ...Collaborate with internal cross-functional teams including R&D, QA, and Customer Success to support smooth delivery of services *...
- ...Technicians), who are responsible for securing equipment operation and GMP (Good Manufacturing Practice) compliance in pilot facility.... ...production teams in the department to technical and IT support as well as QA, fostering strong relationships and open communication Empower...
- ...kliniske forskere, produktionen samt interne samarbejdspartnere (QA, QC, logistik m.fl.). Dine opgaver vil spænde fra den første henvendelse... ..., QA og QC Udarbejdelse og review af dokumentation (GMP/GCP) Sikre rettidig fremstilling og levering af forsøgsmedicin...
- ...Development, analytical teams, Global Contract Manufacturing (GCM), QA, RA, Sourcing, pilot facilities, production facilities, and... ...drying, spray drying and precipitation. High level of relevant GMP experience and understanding of GMP requirements for drug substance...
- ...understanding data from Quality Control (QC) and Quality Assurance (QA). Developing, maintaining, and recommending statistical... ...engineering or a related field. Solid experience in manufacturing, with GMP experience being an advantage. Understanding of scientific...