*Analytical scientist with Experience in Capillary Electrophoresis (CE) and HPLC
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We are seeking a scientist with a strong scientific profile within analysis of proteins focused on HPLC and capillary electropresis techniques in in the Analytical Development (AD) Department at AGC Biologics A/S (AGC). AGC is a Contract Development and Manufacturing Organization with facilities in Denmark, Germany, Italy, Japan and USA and with customers all over the world.
The department
The AD Department is responsible for implementation, transfer and development of analytical procedures, analytical support to upstream and downstream, characterization of products, testing engineering batches for production and the transfer of analytical methods to QC for validation. AGC projects range from early pre-clinical development through all phases of clinical development all the way to commercial supply. AD is also involved in cross functional project groups and implementation of new analytical technologies and techniques.
As a scientist in the analytical development groups you will be using state of the art methods for HPLC, like SEC, IEC, RPC, HIC etc. and electrophoretic techniques, mainly cIEF and CGE . The developed methods will be utilized for analytical support on a wide variety of protein based products to support our customers getting their product to market as fast as possible with a high quality. You will be working together with a team of 4 scientists and 5 technician’s. You will be ADs representative in customer projects, and present the excellent methods implemented results and provide analytical input to discussions.
As a scientist in AD you will be working with a wide variety of tasks ranging from, approval of analytical data, preparation of Report milestones, participation in cross functional project teams and interaction with customers and providing input to method development. We can promise a diverse job with a possibility to get responsibility fast.
The work environment in our department is very informal. There is constant collaboration across the organization, and all employees have a professional and flexible attitude towards their work. The department consists of 40 dedicated and highly competent scientists and technicians working in four sub team; HPLC/CE development, bioassay development, process development support and characterization. The team is in close contact with our counterparts in our Seattle, Heidelberg and Chiba facilities.
Responsibilities and tasks
As a scientist, you will be responsible for multiple methods in many analytical development projects and act as AD project coordinator. You will participate in multi-disciplinary project teams including Upstream, Downstream, Process Transfer, QC, QA and Manufacturing scientists working in close collaboration with the clients’ scientific teams.
You will get the opportunity to work with a broad range of personalities as well as diverse products in different clinical stages and to use your skills in a very cross functional setting and interactive environment.
The job includes:
- Approval and reporting of analytical results to internal and external customers.
- Representation of Analytical Development (AD) in cross-functional project teams.
- Verbal and written reporting to clients.
- Defining product specification together with QC and the client.
- Transfer of analytical procedures to QC.
- Coordinating external testing.
- Strategic technology development together with the department.
Experience and competencies
The ideal candidate holds a master degree or PhD in Protein Chemistry, Biochemistry, Biochemical or Chemical Engineering, or related scientific/technical background with expertise in chromatographic and electrophoretic methods in a protein context. In addition to that you have:
- Strong expertise within analysis of proteins using HPLC and capillary tecniques
- Strong understanding of the workings of analytical instruments and how instrument variables affect assay performance.
- Strong cross-functional expertise and understanding of how analytical methods best capture/monitor potential impacts to the quality and functional activity of proteins during the production process.
- An understanding of biopharmaceutical manufacturing and regulatory requirements.
- Good interpersonal and communication skills.
- Experience from the biopharm industry is not required but is considered an advantage
- Prior experience with leading small teams would be an advantage.
- Excellent English written and oral communication skills.
On a personal level we expect you to:
Be a high performing team player and to be ambitious on behalf of yourself and the company. You master the balance between speed of execution and quality of work. You embrace change and enjoy a rapid pace of work with a positive, can-do attitude and with a good sense of humor. You think of last minute changes as a positive variety in the daily work. You are driven by achieving results through others and are good at presenting results in a convincing manner.
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 "Forsker", og befinder sig i kategorien "Sundhed og forskning".
Arbejdsstedet er beliggende i København
Jobbet er oprettet på vores service den 5.9.2023, men kan have været deaktiveret og genaktiveret igen.
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