|Category||Chemists and Materials Scientists|
|Job type||Full Time|
Are you passionate about improving lives of millions of people by supporting LEO Pharma marketed products?
This is your chance to join one of the world's leading companies within dermatology and to set your mark on the quality of life for millions of patients around the world. LEO Pharma devotes its efforts to developing innovative drugs for the treatment of skin diseases like psoriasis and eczema.
In Quality laboratories you will be a part of making a difference for people around the world with serious skin diseases. You will be part of a dedicated team of 10 people supporting analysis globally. We have an open and informal environment with lots of drive and high professionalism.
We are looking for a Senior Professional, an experienced analytical chemist, who can take on and run tasks related to analytical projects or improvements across teams in the organization.
You solve the tasks by familiarizing yourself with the issues and contributing with your professionalism, with the necessary sparring from the other specialists in the department and organization. You will have a broad interface with the rest of the organization.
Examples of tasks are:
• Professional support for analytical methods that are outsourced to external partners
• Validation of analytical methods and verification of pharmacopeial methods
• Method transfers from LEO Pharma to other laboratories
• Implementation of new methods from R&D to QC
• Trending of results from CMO's
• Support to local release laboratories
• Establishment of new reference substances
• Optimization of procedures
The laboratory has a wide range of analytical equipment, e.g. (U)HPLC, GC, IR, NIR, KF etc.
Further more support to analytical methods for biologics (monoclonal antibodies) will be part of the teams task. On the biological portfolio we work together with external partners and CMOs.
Your qualifications and background
You have a master's degree in science as a chemist, pharmacist, chemical engineer, biochemist or similar.
You have a minimum of 5 years of hands-on experience within analytical chemistry, analytical method validation and method transfers, testing of monoclonal antibodies and experience with gel electrophoresis, bioassays, capillary electrophoresis and similar analytical methods, QC or stability testing and solid experience with GMP.
We work according to GMP, so you must also have the necessary structure and attention to detail to ensure that things are in order.
You have a healthy passion for analytical chemistry and are solidly professionally based. You have a good understanding of regulatory requirements. You have the business perspective to weigh cost and risks in a pragmatic manner.
Regardless of background, you need to be extroverted and good at collaborating with others. You need to be self-driven, focused and able to make decisions. You'd rather talk directly to people than write long emails.
You are able to communicate efficiently in English and Danish/Scandinavian.
You become part of our modern QC laboratory, where you get approx. 75 colleagues who service the entire organization. You will have flexible working hours that are adapted to the tasks. Our environment is characterized by cooperation, openness and space to have fun together. Here is simply nice to be.
Do not hesitate to contact Manager Pernille Thomsen, +4520622399, if you want to know more about the position.
We look forward to receiving your application. Deadline is May 16th2021.