QC LIMS administrator

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 LIMS administrator
Are you looking for an exciting job in an expanding international company producing new biological medicines? Do you thrive in a dynamic environment, in a department with skilled colleagues in an organization where we work as one team?

Then, we have the ideal opportunity for you since Quality Control at AGC Biologics is looking for a quality-minded Administrator for our newly established QC LIMS team.

About the organization
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 development organization, a high level of service to our clients is in focus. AGC is a diverse organization with more than 50 nationalities at site CPH. The corporate language is English.

The QC organization consists of 160 dedicated colleagues, and 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

AGC is growing - we are getting ready to open our new facility next to our existing facility in Søborg. To support the expansion of the QC laboratories, we have established a QC LIMS team. The team is responsible for developing, maintaining, and supporting the use of LIMS across the site. This includes implementing new functionality, updating procedures, training of users, daily support, and more. All activities are performed in compliance with cGMP.

Tasks and Responsibilities
As administrator in QC LIMS, you will be responsible, together with the team, for ensuring that LIMS is operational and that the users can perform their job in the system.

The position requires understating of both the daily operations in a laboratory and the technical aspects of LIMS, so that you can come up with solutions that are practical for the laboratory, while also being technical possible in LIMS.

The Job includes:

• Daily support for the users of the system, both in QC laboratory and manufacturing.
• Implementation of new analysis methods and updating existing analysis to run paperless.
• Updating master data used by the system.
• Testing and validation of new functionality in the system.
• Creation of training material and training of new users.
• Working with other departments for systematic problem-solving and effective solution implementation.

Qualifications
The ideal candidate either holds a degree as technician (Laborant/ Laboratorietekniker) or equivalent and has a solid experience of minimum of 5 years of working in a GMP laboratory, or a master degree in a relevant field such as biology, chemistry, pharmaceutical science, or similar, and has a minimum of 2 years of working in a GMP laboratory.

In addition, we expect you to have:

• Experience working with LIMS (Labware experience is a big plus)
• Good communication and interpersonal skills
• Strong analytical and problem-solving skills and experience applying these skills to resolve technical problems.
• Experience with working in cGMP settings according to European and US regulatory guidelines.
• Capacity to prioritize your own tasks in a dynamic environment.
• Ability to interact positively within a team and in close collaboration with other working areas when needed.

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 humour.

Application
For further information regarding the position, please contact Team Leader Anders Mellerup, QC LIMS, either by email: [email protected] or phone: +45 26894954. We treat the applications as we receive them and conduct interviews with qualified candidates. When the right candidates are found, the add will close.

AGC offers
AGC offers a dynamic working place with good opportunities of working with a varied array of manufacturing tasks and challenges. You will get insight into and experience with the way the various departments throughout a contract manufacturing organization interact to achieve success. Exciting and challenging assignments will constantly come your way, and you will be largely able to plan your daily work yourself. AGC offers an informal working environment, where humour is part of the daily work life. We respect each other and our individual differences. AGC’s employees have a flexible attitude, and we help each other to reach deadlines together as one team.

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.

Location: Copenhagen Site