Temporary Technician, Quality Control

at  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.
QC Bioassay Laboratory Technician, Temporary 12 Months
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.
We are looking for a motivated colleague to join our QC Bioassay department. As an employee in Quality control at AC Biologics in Søborg, you can look forward to a great deal of responsibility and varied work tasks. You can also look forward to being part of a good team in an open and informal environment with solid professionalism, high pace and lots of good laughs.
The Department
The QC organization (QC) consists of five departments: QC Bioassay, QC Chemistry, QC Microbiology, QC Support and QC Planning & Systems. QC is responsible for supporting production of new biopharma-ceuticals by controlling raw materials, performing analytical testing, environmental monitoring of productions rooms, planning and executing stability programs and validating analytical methods according to ICH guidelines from clinical phase I to phase III and commercial.
The position is placed in the QC Bioassay department, we are in total 48 employees, divided into five groups. We perform a broad range of compendial methods, bioassays (e.g. ELISA´s, qPCR, and SDS-PAGE), as well as cell-based assay. 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 of in-process stop/go samples.
Role and 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, SDS-PAGE, qPCR, Octet, Appearance, Solo, OD and Osmolality)
• 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.

Qualifications
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:

• Experience with performance of Bioanalytical methods
• 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.

Application
For further information regarding the position, please contact QC Bioassay Manager Jona Uldahl-Jessen at +45 60253361. 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 candidate are found, the add 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.
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

• Execute a variety of Bioanalytical methods (e.g., ELISA, SDS-PAGE, qPCR, Octet, Appearance, Solo, OD and Osmolality)
• 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