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- ...for competence development and network building Your Skills & Talent Experience from the pharmaceutical industry working in a GMP environment You can demonstrate successful project management skills, preferably in a position as Tech Transfer Lead or CMC Project...
- ...med erfaring med klinisk immunologi. Erfaring med IT-systemet Prosang er en fordel God forståelse for kvalitet og kendskab til GMP Kendskab til dokumentstyringssystemet D4 Du er udadvendt, positiv, har gode samarbejdsevner og et godt overblik Du er fleksibel...
- ...Internal QA Specialist Job openings Deadline October 19, 2025 Department International Quality Assurance Join Pharmacosmos... ...As a QA Specialist, you will play a vital role in ensuring GMP compliance and quality oversight across API production, contract...
- ...for people who share our passion, drive and energy (Genki) to be part of our team in Quality Assurance - Drug Substance Manufacturing (QA DS). As part of the QA intern unit, you will deal with precisely this. Your main purpose will be to help drive a Continuous...
- ...quality processes and engaging in tech transfer projects as the QA responsible for overseeing commissioning and approving qualification... ...to our start-up phase. We prioritize high-quality standards and GMP compliance through close collaboration with our stakeholders. Our...
- ...keep up with this development. We are looking for people who share our passion, drive, and energy (Genki) to be part of our team in QA Data Team. Our Quality Data Team is dedicated to transforming the way we handle quality data across the site. Our mission is to establish...
- ...closely with suppliers and partners, including overseeing and updating Quality Agreements Assisting with training of new employees in QA processes Contributing to regulatory and market access activities, coordinating with production sites and product management...
- ...gennem struktur, analyse og kommunikation? - Så er du måske den nye QA Specialist, vi søger til vores kvalitetsteam hos Nordic Sugar –... .... Fabrikkerne er certificeret efter IFS, ISO/FSSC 22000 og GMP+, og vi arbejder løbende på at integrere standarderne i den daglige...
- ...providing guidance, training, and ad hoc support to stakeholders? Then we hope you are our new colleague! Your New Role As a Senior QA for QC Specialist you will be the primary QA contact for the QC laboratory across all its activities. Your responsibilities will...
- ...documentation. Manufacturing Support consist of approx. 100 employees. In the DSM Documentation team, we provide procedural support to GMP manufacturing and ensure compliance and document release activities in a timely manner. We create and maintain the document package...
- ...are the one we are looking for to lead our technical support and QA across our cell counting instruments. Who are we? ChemoMetec... ..., validation methodologies, and a strong understanding of GMP regulatory requirements is essential to succeed in this role....
- ...Vil du arbejde med høj kvalitetssikring for kunder og leverandører? Så har du nu en unik mulighed for at blive en del af QA-teamet hos Sterigenics i Espergærde – en global leder inden for e-beam-sterilisation Det får du hos Sterigenics En fast fuldtidsstilling i...
- ...oversight and compliance in the production. If this sounds like something for you, then it might be you we are looking to join our QA Drug Substance Team as our new Senior QA Associate. Boost our team You will be part of a competent and supportive QA Drug...
- ...Are you an experienced senior QA specialist with interest in Tech Transfer projects, quality and cross-organizational work? Then you could be our new Project QA for Tech Transfer colleague! Your New Role Our work with many different biopharma companies means that...
- ...class="lg:hidden" Senior QA Engineer - Trackman Broadcast Solution Hørsholm, fulltime_permanent R&D Senior QA Engineer - Trackman Broadcast Solution About the Role Are you passionate about quality and innovation in live sports technology? We're looking...
- ...Matter Expert to join our QC Sample Control team, bringing extensive GMP experience and a talent for improvements and optimizations. If... ...of Analysis (CoA) Collaborate with stakeholders and QA to create and maintain GMP documents Initiate deviations and assist...
- ...well as external stakeholders (Production, Planning, Supply Chain, QA, Procurement). Your Impact In this critical role, you will... ..., Supply Chain, or related field Solid background in GMP-regulated environments (QC, Supply Chain, or Production) Strong...
- ...looking for new colleagues for both our Upstream- and Downstream-QA teams Your New Role You will be pivotal in ensuring seamless... ...Knowledge ~+ 3 yrs experience in Good Documentation Practice, GMP, quality systems and legislation ~ a university degree in a scientific...
- ...employees across Drug Substance, Drug Product, Warehouse, QC, and QA operations. This role is pivotal in ensuring robust, compliant,... ...strategic leadership with hands-on operational engagement, ensuring GMP compliance, driving continuous improvement, and fostering a...
- ...quality and audit team as we are currently looking for a new dedicated QA spirited colleague! Your New Role Through your sound... ...audit experience. Preferably you have practical experience with EU GMP, cGMP and IT audits from diverse positions within the biotech/ pharmaceutical...
- ...clinical and commercial batches. You will liaison with the operational QA DS teams, DS Manufacturing Support, Process Science and QC on... ...the batch has been manufactured and tested in accordance with GMP regulations and quality agreements. To perform QP statements in...
- ...and internal stakeholders Support maintenance of the approved GMP supplier list Support and coordinate TrackWise workflows and maintain... ...degree within life science) ~3-5 years of experience with GxP QA and supplier/auditing management, project related work ~ We are...
- ...Du har arbejdet med udfærdigelse, revision og review af procedurer og records Du har erfaring med Good Manufacturing Processes (GMP) Du synes at arbejdet med LEAN og drift er interessant Hvem er vi? ChemoMetec er en af verdens førende producenter af udstyr...
- ...process development, troubleshoot critical experiments, and validate key findings. Finally, you will collaborate with Quality Assurance (QA), Regulatory Affairs, Analytical, Manufacturing teams, CDMOs to align and support the development efforts with overall business...
- ...Administration, Supply Chain Management or similar ~ UpToDate knowledge of common customs rules and regulations, and experience with GDP/GMP ~ Knowledge about Shipping Qualifications is an advantage We Hope You Are: A natural leader who thrives by being part of...
- ...lead for introduction and implementation for cell culture processes of new programs from customers into our large-scale manufacturing GMP facilities. You will be the upstream subject matter expert (SME) on projects and programs and have the direct interface with...
- ...Gerne flere års praktisk erfaring fra et lignende produktionsmiljø. Har erfaring med produktion af medicinsk udstyr, herunder GMP og GDP. Har kendskab og erfaring med automatiske anlæg, herunder robotstyring og automatiske pakke-celler. Stærke samarbejdsevner...
- ...Manufacturing Organization (CDMO) serving customers in the pharmaceutical industry – from pre-clinical investigations to commercial GMP production. The Principal Database Administrator (PDBA) is the global strategic and technical lead on the design, build, management...
- ...samarbejde med kollegaer på vores laboratorier i Kolding og Karise, samt vores fabrikker og lagre rundt om i landet. Du referer direkte til QA-chefen og bliver en vigtig brik i at sikre og udvikle vores kvalitetsarbejde på tværs af hele organisationen. Arbejdsopgaver...
- ...Development Manufacturing Organization (CDMO), der har kunder i den farmaceutiske industri – fra prækliniske undersøgelser til kommerciel GMP-produktion. For at supportere vores mange nye kunder, søger vi nu en laborant til metodeoverførelse af kundernes kemiske...