Scientist, QC Lab
at Genmab
København, Region Hovedstaden, Denmark -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 21 Apr, 2025 | Not Specified | 22 Jan, 2025 | 5 year(s) or above | Validation,Elisa,It,Analytical Instruments | No | No |
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Description:
At Genmab, we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our business, which is innovative and rooted in science, we believe that being proudly unique, determined to be our best, and authentic is essential to fulfilling our purpose.
REQUIREMENTS
- It is expected that you have a master’s degree in natural science, pharmacy, or similar.
- You have at least 5 years of documented professional experience with analytical methods in a GMP QC setting.
- You have a thorough understanding of the detailed requirements for analytical validation and are up to date with current trends.
- Experience with qualification of analytical instruments is desirable.
- You have active and recent experience within analytical development and validation of methods for biologics/monoclonal antibodies from a phase II/III program.
- You have experience with various biochemical and physico-chemical analyses (i.e HPLC, CE-SDS, icIEF or ELISA).
This role is based in Ballerup and is on-site.
Responsibilities:
THE ROLE & DEPARTMENT
As QC Scientist at Genmab, you will be part of a GMP QC Laboratory in Ballerup. The laboratory is responsible for supporting Genmab’s innovative products by performing release and stability testing according to ICH guidelines. It is newly established, and we are a currently a larger group of Scientists and Technicians.
The position reports to the Associate Director, Team Lead, Quality Control Laboratory.
KEY RESPONSIBILITIES INCLUDE
- Review release and stability data.
- Support and train fellow scientists and laboratory technicians.
- Author and review initial laboratory procedures.
- Implement, qualify, and maintain laboratory equipment.
- Validate analytical methods.
- Collaborate and participate in cross-site training with the Analytical Development group in Utrecht, NL, and the Analytical Subject Matter Experts (SMEs) in Copenhagen.
REQUIREMENT SUMMARY
Min:5.0Max:10.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
IT
Proficient
1
København, Denmark