Experienced analytical Scientist for drug formulation research & development
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Hørsholm
Do you have experience with analytical development in CMC, and want to expand your knowledge of drug discovery in a fast paced and ambitious biotech?
Gubra is looking for an experienced analytical scientist to support our drug discovery and drug development projects. In this role you will evaluate physicochemical stability of peptides for our internal drug discovery projects and contribute to our clinical development team with critical support and troubleshooting of analytical methods for drug substance and drug product at CROs and CDMOs.
Gubra is an ambitious biotech company striving for excellence at all levels. We insist on doing things efficiently – and often differently - to reach the results we aim for. Our vision is to become leaders in the fight for a more sustainable and healthier world. We do that by facilitating the discovery of new medicine, and by acting and inspiring others to fight against the ongoing climate and biodiversity crises.
The Drug Profiling department supports the Gubra drug discovery & development projects by delivering physicochemical characterization, early formulation development, analytical support, bioanalysis and PKPD analysis for novel peptide drug candidates. Furthermore, we support the Contract Research Organization (CRO) with bioanalysis for in vivo pharmacology experiments. We are currently 5 scientists and 4 laboratory technicians in the department.
You have solid experience with and a strong interest in analysis of peptide drug substance and drug product with a specific focus on HPLC methods (mainly SEC, RP). Knowledge of LC-MS is advantageous. You enjoy collaborating with laboratory technicians and scientists with different backgrounds and you thrive in a fast-paced environment. Experience with CRO/CDMO interaction and tech transfers is an advantage.
As Analytical Scientist in Drug Profiling, your tasks will include:
Professional qualifications:
As a person you are
Please apply no later than March 1st, 2024, by uploading your motivated cover letter, resume and relevant diplomas on our website. We will invite candidates for interviews continuously, so we look forward to hearing from you as soon as possible. If we find the right candidate, we will close the job before the deadline. If you have questions about the position, please contact Department Manager Jakob Plum Christensen ([email protected] or phone +4522935784).
About Gubra
Gubrais an ambitious CRO & Biotech company striving for excellence at all levels. We insist on doing things efficiently – and often differently - to reach the results we aim for. Our vision is to become leaders in the fight for a more sustainable and healthier world. We do that by facilitating the discovery of new medicine, and by acting and inspiring others to fight the ongoing climate and biodiversity crises.
We have two primary areas of business: Preclinical contract research (CRO) services, as well as peptide drug discovery partnerships. We generate our revenue by performing research for life science companies as well as by partnering projects from our discovery and development pipeline.
Our therapeutic focus is within metabolic and fibrotic diseases, and we specialize in in vivo pharmacology, ex vivo assays, drug profiling, histology, stereology and whole brain and organ imaging. In addition, we offer a full palette of advanced transcriptomics. Our ML/AI-driven peptide drug discovery platform streaMLine enables us to rapidly develop a peptide hit into a non-clinical candidate ready for development. Through a constant focus on high quality, scientific excellence, speed, and solid teamwork we have established ourselves as a highly professional and competent partner in the market.
People are our greatest asset, and our team consists of +220 employees all located in Hørsholm, Denmark. The mix of people from different cultures and educational backgrounds combined with our entrepreneurial mindset have greatly impacted our working environment, which is characterized by drive, scientific curiosity, and teamwork – we join forces!
Gubra is looking for an experienced analytical scientist to support our drug discovery and drug development projects. In this role you will evaluate physicochemical stability of peptides for our internal drug discovery projects and contribute to our clinical development team with critical support and troubleshooting of analytical methods for drug substance and drug product at CROs and CDMOs.
Gubra is an ambitious biotech company striving for excellence at all levels. We insist on doing things efficiently – and often differently - to reach the results we aim for. Our vision is to become leaders in the fight for a more sustainable and healthier world. We do that by facilitating the discovery of new medicine, and by acting and inspiring others to fight against the ongoing climate and biodiversity crises.
The Drug Profiling department supports the Gubra drug discovery & development projects by delivering physicochemical characterization, early formulation development, analytical support, bioanalysis and PKPD analysis for novel peptide drug candidates. Furthermore, we support the Contract Research Organization (CRO) with bioanalysis for in vivo pharmacology experiments. We are currently 5 scientists and 4 laboratory technicians in the department.
You have solid experience with and a strong interest in analysis of peptide drug substance and drug product with a specific focus on HPLC methods (mainly SEC, RP). Knowledge of LC-MS is advantageous. You enjoy collaborating with laboratory technicians and scientists with different backgrounds and you thrive in a fast-paced environment. Experience with CRO/CDMO interaction and tech transfers is an advantage.
As Analytical Scientist in Drug Profiling, your tasks will include:
- Evaluate physicochemical stability of peptides using high-throughput plate-based assays (fluorescence, UV, turbidity, DLS) and/or HPLC.
- Go-to HPLC expert at Gubra.
- HPLC method development and troubleshooting for drug discovery projects.
- Support the clinical development team with HPLC-method development, analytical tech transfer and troubleshooting.
- Continue developing our analytical capabilities at Gubra.
- Focus on automatization of laboratory tasks.
Professional qualifications:
- PhD degree within biochemistry, chemistry, pharmaceutics, engineering, or similar
- 3-5 years relevant experience with analytical development for drug development projects.
- Experience with HPLC method development and maintenance.
- Experience with coordination of technician’s tasks.
- Great execution and collaboration skills.
- Good communication skills.
As a person you are
- Keen to take on responsibility.
- A true team player and eager to contribute to all workflows in the department.
- Proactive and able to initiate, focus and deliver on tasks and projects.
- Able to navigate and collaborate in an energetic and rapidly changing organization.
Please apply no later than March 1st, 2024, by uploading your motivated cover letter, resume and relevant diplomas on our website. We will invite candidates for interviews continuously, so we look forward to hearing from you as soon as possible. If we find the right candidate, we will close the job before the deadline. If you have questions about the position, please contact Department Manager Jakob Plum Christensen ([email protected] or phone +4522935784).
About Gubra
Gubrais an ambitious CRO & Biotech company striving for excellence at all levels. We insist on doing things efficiently – and often differently - to reach the results we aim for. Our vision is to become leaders in the fight for a more sustainable and healthier world. We do that by facilitating the discovery of new medicine, and by acting and inspiring others to fight the ongoing climate and biodiversity crises.
We have two primary areas of business: Preclinical contract research (CRO) services, as well as peptide drug discovery partnerships. We generate our revenue by performing research for life science companies as well as by partnering projects from our discovery and development pipeline.
Our therapeutic focus is within metabolic and fibrotic diseases, and we specialize in in vivo pharmacology, ex vivo assays, drug profiling, histology, stereology and whole brain and organ imaging. In addition, we offer a full palette of advanced transcriptomics. Our ML/AI-driven peptide drug discovery platform streaMLine enables us to rapidly develop a peptide hit into a non-clinical candidate ready for development. Through a constant focus on high quality, scientific excellence, speed, and solid teamwork we have established ourselves as a highly professional and competent partner in the market.
People are our greatest asset, and our team consists of +220 employees all located in Hørsholm, Denmark. The mix of people from different cultures and educational backgrounds combined with our entrepreneurial mindset have greatly impacted our working environment, which is characterized by drive, scientific curiosity, and teamwork – we join forces!
Information og data
Denne ledige stilling har jobtypen "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Hørsholm.
Jobbet er oprettet på vores service den 14.2.2024, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Forretningsudvikler
- Hørsholm
- Fredag den 01. marts 2024
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