Quality Control Experienced Scientist

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AGC Biologics is a leading global Contract Development and Manufacturing Organization, with a deep commitment to improving life quality by bringing new biopharmaceuticals to market. Because of our dedication to building and empowering our internal teams, AGC Biologics is an innovative leader in the industry with an extensive network of cGMP facilities in the US, Europe and Asia. As such, we deliver a deep expertise, dynamic solutions and technologies, as well as customized services for the scale-up and cGMP manufacturing of protein-based therapeutics. We forge exceptionally strong partnerships with our clients, and we never lose sight of our pledge to deliver a reliable and compliant drug substance supply. Right. On time. For more information, visit www.agcbio.com.

Quality Control Experienced Scientist

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

The Department
The QC department at AGC Biologics consists of 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, many different customers’ projects and with various biopharmaceuticals the QC department differs from traditional QC labs. The position requires an engaged, ambitious employee and in depth knowledge within analytical. QC have a close collaboration with customers, and departments across the organization to gain control of all steps in the manufacturing processes.

Tasks and Responsibilities

The position is within QC Chemistry and requires technical expertise and ability to troubleshoot on chromatographic methods, especially HPLC, iCIEF and CGE -SDS, and expertise within (U) HPLC equipment. A major part of the job will be representation of QC in customer project teams, preparing for method validation (clinical phase I/II through full validation) and commercial licensing. You will have contact with customers with diverse backgrounds and cultures; for that reason good communication skills are essential. Cooperation with the customers will at times be very close, and will have consultative character in order to solve customer challenges together. Design and implementation of test method validations, including report writing and review, along with managing projects are also important parts of the job. On a daily basis, the tasks also include improvement of laboratory GMP systems according to European and US regulatory guidelines. QC Chemistry is looking for an engaged and ambitious person, willing to go the extra mile.

Your Profile

The ideal candidate holds a MSc or PhD degree in Biochemistry, Chemistry or relevant area and has after obtained degree, minimum 5 years of work experience in analytical development or quality control. In addition, we expect you to bring some of the following experience and characteristics:
• Working and troubleshooting experience with SE-, IEX- and RP-UHPLC, iCIEF and CGE-SDS analysis.
• Experience with writing validation protocol, validation report, SOP’s is an advantage
• Experience and knowledge with (U)HPLC equipment and Chromeleon software
• Technical experience in protein analytics testing
• Knowledge of protein structure and biochemistry
• You like to share your knowledge and communicate openly and professionally both internally and with external customers
• The ability to handle multiple tasks simultaneously without losing track
• You are a team player combined with the ability and desire to work independently
• You enjoy working in a high pace and be challenged in a busy business
• Excellent communication, presentation and interpersonal skills.
• Knowledge of GMP systems according to European and US regulatory guidelines is an advantage
• Ability to apply organizational skills to systems and efficiency improvement.

AGC has international customers and our company language is English. It is therefore vital to be fluent in written and spoken English.

AGC offers
AGC offers a dynamic workplace with good opportunities to work with a wide and varied range of tasks and challenges. You will be inaugurated in and have experience with the way the various departments in a "Contract Manufacturing Organization" (CMO), collaborate to achieve success. Exciting and challenging assignments will come to you in a steady stream, and you will very largely able to plan your day. AGC offers an informal and humorous working environment that is characterized by the fact that we think it is fun to go to work. We respect each other and our differences. AGC employees are flexible and take pride in working together to achieve goals - as one team.

For further information regarding the position, please do not hesitate to contact Director QC Chemistry, Iben Schildt Sørensen, telephone +45 2294 2949.
We will process the applications as they arrive. Therefore please submit your application and CV as soon as possible and no later than December 21, 2019. We treat the applications as we receive them, and qualified applicants can expect to be interviewed before the deadline.


Information og data

Denne ledige stilling har jobtypen "Laborant", og befinder sig i kategorien "Sundhed og forskning".

Arbejdsstedet er beliggende i København

Jobbet er oprettet på vores service den 9.12.2019, men kan have været deaktiveret og genaktiveret igen.

Rapportér
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
  • Laborant
  • København
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