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reference: 5025825

documentId: 5025825

connectionPointId: 7

lastModificationDate: 1565008226063

stillingsbetegnelse: Technician for QC Chemistry

jobbeskrivelse:

Technician for QC Chemistry, working with Raw Materials and Chromtagraphic analysis 

Join a dynamic and international company where everyone is responsible for delivering right on time as one team! 

QC Chemistry is looking for a Technician in a new position, covering two areas: 1) Raw material for manufacturing and 2) Chromatographic analysis to support manufacturing and stability studies. 

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.

 

The Department

The QC department at AGC Biologics includes three functional groups: QC Bioassay, QC Chemistry, and QC Microbiology. The QC groups are responsible for supporting the production of new biopharmaceuticals by controlling raw materials, performing analytical methods, planning and executing stability programs and validating various analytical procedures according to ICH guidelines from clinical phase I to phase III and commercial.

Within this broad working area and with various biopharmaceuticals, QC works in close collaboration with departments across the organization to gain control of all steps in the manufacturing processes. 

 

Tasks and Responsibilities

As a Technician in QC Chemistry, Raw Materials and Chromatographic you will be responsible for the sampling and NIR testing of raw materials to manufacturing, as well as performing HPLC analyses, such as RP-HPLC, SE-HPLC, HI-HPLC, cIEX-HPLC, CE-SDS and iCIEF analyses. 

The position requires 2-3 days in raw materials and 2-3 days in Chromatographic analysis on a weekly basis.  

QC Chemistry performs both raw material control for manufacturing, analyses of the production and stability studies of the API and validation of analytical methods for clinical phase I/II and III. The work is conducted in accordance with cGMP. You will be responsible for equipment in QC and are to ensure that existing procedures and guidelines are being followed.

 

Your Profile

We expect you to hold a degree as Laboratory Technician or similar and that you bring several years of work experience within raw materials and/or in analytical development or quality control. In addition, we expect you to have:

• Experience with sampling of Raw materials.

• Experience with NIR analyses of raw materials.

• Technical experience in (U)HPLC analyses, iCIEF and/or CE-SDS.

• Experience with working in a GMP environment.

• Good communication and interpersonal skills.

• An ability to interact positively within a team and in close collaboration with other working areas when needed.

Applicants with practical experience in Raw materials and/or HPLC, iCIEF and/or CE-SDS analyses will be preferred.

It is important that you have a self-driven 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.

 

AGC offers

AGC offers a dynamic working place with good opportunities of working with a varied array of tasks and challenges. You will get insight into and experience with the way various departments in a contract manufacturing organization interact in order to achieve success. Further, exciting and challenging assignments will constantly come your way, and you will to a large extend be able to plan your daily work yourself. AGC offers an informal working environment, where humor 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 a team. 

Please submit your application as soon as possible and not later than August 25^th 2019. We review the applications continuously, and qualified applicants can expect to be invited to an interview before the deadline. 

For further information regarding the position, please do not hesitate to contact Director, QC Chemistry, Iben Schildt Sørensen, telephone +45 2294 2949.

numberOfPosts: 1

jobCategoriesCodes_0: http://data.europa.eu/esco/isco/C2145

abstractJV_contact_0: Please apply using one of the specified channels

positionTypeCode: directhire

contractTypeCodes_0: fulltime

Arbejdsgiver Navn: AGC Biologics A/S

source: DK-STAR