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Senior LIMS Specialist for Global QC Development
In this role you’ll make an impact by working as a Senior LIMS Specialist in our team, where you will take part in management of projects for LIMS changes across QC laboratories and other stakeholders including implementation, documentation and communication.
Future projects could be introducing and validating LIMS solutions on new equipment or technologies, new LIMS functionalities, improving and aligning existing processes.
Laborant eller procesoperatør til bufferproduktion til cancerdiagnostik
Vil du bidrage til diagnostik af cancer og gøre en forskel for patienter? Bliver du motiveret af laboratoriearbejde i et travlt produktionsmiljø? Er du detaljeorienteret og lægger vægt på korrekt produktion og dokumentation?
Vores hverdag består hovedsagelig af produktioner, grundig dokumentation og reviews men vi prioriterer også tid til løbende forbedringer af vores arbejdsgange og processer.
Der er tale om en fuldtidsstilling på 37 timer per uge. Arbejdstiden ligger i dagtimerne og vi har flextid.
Technical Writer to GE HealthCare Denmark
Join GE HealthCare to help develop high quality instructions for use for our ultrasound scanners, transducers, and reprocessing methods in compliance with rules and legislation in various countries. This is your opportunity to become part of an innovative team where your work has a real impact on people’s lives around the world.
Our Technical Documentation team consists of six dedicated and passionate specialists with a mix of seniority, educational backgrounds, and nationalities. Our Technical Writers develop and maintain the user documentation for our high-performance equipment.
Continuous Improvement Partner
As a Continuous Improvement Partner in Drug Substance Manufacturing, you will be part of a team of Improvement Partners who develops and sustains systems and tools that enables the organization to consistently increase the level of operational excellence in manufacturing.
Your primary tasks will include but not be limited to:
- Develop and sustain CI systems and tools.
- Coach on ideal behaviour that drives a proactive improvement culture.
Protein Chemist for production of antibodies for cancer diagnostics
Do you find antibody production exciting?
You will play a key role in daily support of the production of conjugates. This can include:
- Support lab techs in case of technical issues with purification, conjugation, and test of antibodies.
- Handle compliance issues according to GMP standards.
We offer a high degree of freedom and development opportunities in an international company.
Laborant til Incoming QC
Vil du bidrage til diagnostik af cancer og gøre en forskel for patienter? Er du detaljeorienteret og lægger vægt på korrekt produktion og dokumentation? Trives du i et spændende produktionsmiljø?
I Incoming Quality Control (IQC) foretager vi kvalitetskontrol af råvarer og Outsourced supplier materials, hvor vi sikrer at den korrekte dokumentation er tilstede, før vi godkender råvarerne til produktion. Desuden foretager vi test af nogle råvarer, ELISA tests, Bioburden og analyser af vandprøver.
Hverdagen består hovedsageligt af grundig kvalitetskontrol af dokumentation og reviews samt laboratoriearbejde, men vi prioriterer også tid til løbende forbedringer af vores arbejdsgange og processer.
Coordinator in Quality
Are you our new coordinator within Quality? Do you enjoy working with Planning & Forecasting, Contract Laboratory Organization (CLO) management, Reference standard & Control management - then join our Data Management team within Quality in our site in Hillerød.
You will be the point of contact for CLO´s used within Quality Control (QC) ensuring the relationship and making sure contracts are in place. Your responsibilities will include monitoring of inventory levels, providing status to management and facilitating the timely delivery of products to customers.
EU Clinical Advisor – Data Management
We are looking for a Clinical Advisor with deep clinical data management or clinical informatics expertise who wishes to make a mark on some...
Scientist for QC Raw Materials Analytical Management Team
We are looking for a scientist that understands the quality setup of a QC laboratory in a GMP environment.
Instrument Maintenance Coordinator for QC Instrument Support
Are you a good coordinator with a big picture mind-set and “can-do” attitude who thrives in an environment where close collaboration involving multiple stakeholders is key?
