*QC Equipment Technician
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Then, we have the ideal opportunity for you since Quality Control at AGC Biologics is looking for a quality-minded Technician for our newly established QC Equipment department.
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.
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 building a new facility next to our existing facility in Søborg. To support the expansion of the QC laboratories, we have established a QC Equipment Department. The department is owner of all equipment in QC and responsible for life cycle management activities such as preparation of URSs, procurement, qualification, maintenance, (re)qualification/calibration, and decommissioning. All activities are performed in compliance with cGMP.
Tasks and Responsibilities
As Technician in QC Equipment, you will be responsible for ensuring that analytical instruments are being kept in compliance and in operational order to allow for our continuous analytical testing.
The Job includes:
- Performing maintenance of analytical instruments such as HPLCs, CEs, NIR, ELISA readers, SoloVPE, qPCR instruments etc.
- Maintaining other types of equipment like climate chambers, pipettes, balances etc.
- Working closely with other departments for systematic problem-solving and effective solution implementation.
- Maintaining assigned maintenance records, work orders, and service agreements in an orderly and accurate manner.
- Assisting in qualification activities.
The position requires hands-on experience with instrument maintenance. All work in the department is performed under cGMP and you will be responsible for finalizing service reports and enter work performed in the equipment database.
Qualifications
The ideal candidate holds a degree as laboratory technician (Laborant/Laboratorietekniker) or equivalent and has a solid experience of minimum of 3 years of working in a GMP laboratory. In addition, we expect you to have:
- (Technical) experience with life cycle management of analytical equipment such as HPLC, iCIEF, CE-SDS, ELISA readers, SoloVPE, and qPCR instruments
- 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.
- Good communication and interpersonal skills
- 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 Manager Johan Bollhorn, QC Equipment, either by email: [email protected] or phone: +45 20808924. We treat the applications as we receive them and conduct interviews with qualified candidates. When the right candidates are found, the add will close - please make sure to upload both CV and cover letter when applying.
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 to a large extent be 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.
Want to keep posted about our growth and to learn more about our company?
We also urge you to follow us on our LinkedIn Company Page and give us a quick Like on Facebook !
AGC Biologics (AGC) is a global Contract Development Manufacturing Organization (CDMO) with bio-manufacturing facilities in Europe, Japan, Italy and the USA. The company provides a comprehensive range of commercial and clinical cGMP biologics manufacturing services, from DNA to active pharmaceutical ingredient (API). The company’s team and approach are tailored to each of its client’s needs, whether turnkey manufacturing or sophisticated, stand-alone analytical, formulation and stability services.
Visit www.agcbio.com to learn why AGC Biologics is a World Leader in process development and contract manufacturing.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i København
Jobbet er oprettet på vores service den 18.1.2024, men kan have været deaktiveret og genaktiveret igen.
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