Powered by
AGC Biologics
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.
Do you thrive in a dynamic environment, in a department with skilled colleagues in an organization where we work as one team? If yes – you may want to join our department as Technician (Laborant) in QC Chemistry and be part of a growing global CDMO. QC Chemistry at AGC Biologics A/S is expanding and looking for a Technician for Chromatographic Analysis to support manufacturing and stability studies.
This is a temporary position for 12 months, as a Technician (Laborant) for Quality Control (QC) Chemistry, for the Chromatographic Analysis team.
The QC Chemistry department:
At AGC Biologics A/S (AGC), we work with the development of biopharmaceutical manufacturing processes and GMP manufacturing of biopharmaceutical proteins for both clinical testing and marketing. Since we are a contract manufacturing organization, a high level of service to our clients is in focus.
QC Chemistry is one of five departments in the QC area, where we are responsible for supporting the production of new biopharmaceuticals by performing analytical testing of samples from the production and stability programs and validating various analytical procedures according to ICH guidelines from clinical phase I/II to phase III and commercial.
Within this broad working area and with various biopharmaceuticals, the QC area has a close collaboration with all departments across the organization.
Role & responsibilities:
As Technician in QC Chemistry, you will be responsible for performing chromatographic analysis such as RP-UHPLC, SE-UHPLC, HIC-UHPLC, cIEX-UHPLC, peptide mapping, CE-SDS and iCIEF. Specifically for this 12-month temporary position, CE-SDS will be the focus area.
QC Chemistry performs analyzes for manufacturing and stability studies of the API and validation of analytical methods for clinical phase I/II and III. All work is performed under cGMP and you should help to ensure that existing procedures and guidelines are followed.
Your Profile:
We expect you to hold a degree as Laboratory Technician or similar, and bring relevant work experience as a Laboratory Technician. In addition, we expect you to have:
It is important to have a self-motivating personality with a pragmatic attitude and approach to the daily work - without compromising quality. Furthermore, you thrive in a challenging and dynamic environment and enjoy a rapid pace of work. You bring a positive, can-do attitude and a good sense of humor.
Your Application:
Due to some holidays in the hiring team, relevant candidates can expect to be called by Talent Acquisition from Monday March 17 and onwards. We are planning to conduct interviews until the end of March, and aiming to hire the right candidate before April, with a start date as soon as possible. We are looking very much forward to receiving your application! When the right candidates are found, the ad will close.
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 2,500 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 www.agcbio.com. 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.
