QC Bioassay Laboratory Technicians
Copenhagen - Denmark
Job Summary
Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients lives by bringing new biopharmaceuticals to market.
QC Bioassay Laboratory Technicians
Location: Søborg Capital Region Denmark Denmark
Are you looking for an exciting job in a fast-growing international company producing new biological medicines Do you thrive in a dynamic environment with lots of exiting challenges every day Do you want to be part of a team of skilled colleagues and in an organization where we work as one team QC Bioassay is looking for 3 laboratory Technicians (laboranter) to be part of our technician team.
AGC Biologics A/S is a global CDMO where we work with the development of biopharmaceutical manufacturing processes and GMP manufacturing of biopharmaceutical proteins for both clinical testing and marketing. We are working in an international and customer-oriented way to secure fast and reliable manufacturing of medicines to our customers.
The Department
The position is placed in QC Bioassay which is one of five departments in our QC QC Bioassay we are in total 51 employees both scientists and technicians divided into four groups - Bioassay Scientists Bioassay Technicians Bioassay Cell & Reference Material and General Analytics. We perform a broad range of compendial methods bioassays as well as cell-based assays. We are responsible for method validations for early and late stage products release testing of clinical and commercial batches (DS and DP) as well as testing of stability samples. Finally but not least we are responsible for supporting the 24/7 operating manufacturing of biopharmaceuticals by testing in-process stop/go samples.
Responsibilities
As a technician in QC Bioassay you will be involved in analytical testing of drug substance and drug product samples as well as in-process samples. Moreover you will be involved in stability programs and validation of methods used for phase I/II and phase III/Commercial products.
Main responsibilities:
Execute a variety of Bioanalytical methods (e.g. ELISA Octet qPCR and cell-based assays)
Report results including data processing in LIMS and setup.
Participate in method validation studies.
Participate in troubleshooting of methods.
Participate in on-time testing of stop/go samples to support our manufacturing facility.
All testing is performed according to the cGMP
Your Profile
The ideal candidate holds a degree as laboratory technician (laborant). We expect you to have a structured mindset be able to work independently and meet tight deadlines with a can-do attitude but without compromising the quality.
In addition we expect you to bring some of the following experience and characteristics:
It will be an advantaged to have an experience with Elisa and Celle based assays
Experience working in a cGMP setting according to European and US regulatory guidelines.
Good communication skills and a service-minded attitude as you will work closely with your stakeholders mainly form the manufacturing.
Has a flair for teamwork combined with the ability and desire to work independently.
The ability to handle multiple tasks simultaneously in a busy environment.
Fluent in written and spoken English.
We Offer
A permanent 37-hour position in a well-functioning team with an informal work environment close collaboration and the opportunity to gain broad insight into how a bioassay department operates within an international contract manufacturing organization.
AGC Biologics offers a dynamic workplace with strong opportunities for professional development and daily contact with colleagues across the organization. We offer an informal work environment where humor is part of everyday life and where we respect each other and our differences. We help each other to reach our goals together as a team.
We treat the applications as we receive them and conduct interviews with qualified candidates. Please submit your application as soon as possible. When the right candidates are found the add will close.
For further information regarding the position please contact QC Bioassay Manager Jona Uldall- Jessen: Phone 45 between 16:00-17:00
Our culture at AGC Biologics is defined by the six core values: Knowledge Trust Quality Ingenuity Accountability and Teamwork. Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe.
AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins plasmid DNA (pDNA) messenger RNA (mRNA) viral vectors and genetically engineered cells. Our global network spans the U.S. Europe and Asia with cGMP-compliant facilities in Seattle Washington; Boulder and Longmont Colorado; Copenhagen Denmark; Heidelberg Germany; Milan Italy; and Chiba Japan. We currently employ more than 2500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients most complex challenges including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more visit.Want to keep posted about our growth and learn more about our company Follow us on LinkedIn and give us a quick Like on Facebook!
AGC Biologics offers a highly competitive compensation package and a friendly collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age ancestry color family or medical care leave gender identity or expression genetic information marital status medical condition national origin physical or mental disability political affiliation protected veteran status race religion sexual orientation or any other characteristic protected by applicable laws regulations and ordinances.
Our culture at AGC Biologics is defined by the six core values: Knowledge Trust Quality Ingenuity Accountability and Teamwork. Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe.
AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins plasmid DNA (pDNA) messenger RNA (mRNA) viral vectors and genetically engineered cells. Our global network spans the U.S. Europe and Asia with cGMP-compliant facilities in Seattle Washington; Boulder and Longmont Colorado; Copenhagen Denmark; Heidelberg Germany; Milan Italy; and Chiba Japan. We currently employ more than 2500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients most complex challenges including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more visit.Want to keep posted about our growth and learn more about our company Follow us on LinkedIn and give us a quick Like on Facebook!
AGC Biologics offers a highly competitive compensation package and a friendly collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age ancestry color family or medical care leave gender identity or expression genetic information marital status medical condition national origin physical or mental disability political affiliation protected veteran status race religion sexual orientation or any other characteristic protected by applicable laws regulations and ordinances.
Required Experience:
IC