Innovation Scientist (Postdoc, Chemiker), 100% (m/w/d) — CordenPharma
- Location
- Liestal
- Contract
- full-time
- Posted
- 36 days ago
Role overview
CordenPharma is one of the leading Contract Development and Manufacturing Organizations (CDMO) and develops and produces pharmaceutical active ingredients, drugs and related packaging services on behalf of its customers as a “full-service” service provider. The group employs around 3,500 people. Our network in Europe, Asia and the USA offers flexible and specialized solutions for six technology platforms: Peptides, Lipids & Carbohydrates, Injectables, Highly Potent & Oncology, Small Molecules and Oligonucleotides. We strive for excellence in supporting this network and are committed to providing the highest quality products for the benefit of patients. Our People Vision: We strive for excellence. We share our passion. Together, we make a difference in patients’ lives. Innovation Scientist (Postdoc, Chemist), 100% (m/f/d) Duration 12 months with possibility of extension.
- Liestal
- By agreement
- Full time
- 1 year temporary
Your exciting task area We are looking for a committed and research-strong personality with a strong hands-on mentality. Subordinated directly to Team Leader Lipid Development, you will be responsible for the development and practical implementation of the synthesis of novel lipids and related molecular classes to expand our lipid portfolio for pharmaceutical applications.
- Independent development of novel lipids and related molecular classes from route finding to synthesis and process development to chromatographic purification (MPLC, preparative HPLC), isolation and scaling on a 10-100 g scale
- Close cooperation with all departments involved for the successful implementation of development projects
- Introducing new, creative synthesis methods and concepts
- Participation in scientific cooperation with external partners is desired
- Responsible for the timely preparation of all necessary documentation (technical production and status reports, etc.)
- Communication of all technical aspects to internal stakeholders.
Your profile
- Completed doctorate in organic chemistry not more than 3 years ago
- Broad knowledge and practical experience in the synthesis chemistry of complex organic molecules and solid basic knowledge in physical chemistry. Knowledge of lipid chemistry, peptide chemistry or related specialties is advantageous
- Ability to critically evaluate scientific literature and independently develop new synthetic pathways
- Proven ability to independently identify, analyze and pragmatically solve complex synthesis and cleaning problems
- Scientific curiosity with hands-on mentality and pleasure in independent experimental work
- Enjoying practical laboratory work, as well as carrying out syntheses, processing and purification on a 10-100 g scale
- Good analytical knowledge, especially in NMR, HPLC and LC-MS and interpretation of analytical data sets. Experience with CAD detectors is an advantage
- High degree of initiative and the ability to drive development projects largely independently
- Excellent analytical thinking skills and quick comprehension
- Careful documentation of experiments, independent preparation of technical reports
- Structured evaluation and presentation of results
- Teamwork, initiative action and very independent and committed work
- Communication ability, process-oriented thinking and action
- Excellent knowledge of German and English.
An attractive workplace with a high level of responsibility Short distances and direct communication with all departments Appreciative working environment Corden Pharma offers you interesting and versatile tasks in a highly motivated team. Through a practice-oriented training, we help you quickly gain professional security in order to work independently with a high level of personal responsibility.
- Completed doctorate in organic chemistry not more than 3 years ago
- Broad knowledge and practical experience in the synthesis chemistry of complex organic molecules and solid basic knowledge in physical chemistry.
- We strive for excellence in supporting this network and are committed to providing the highest quality products for the benefit of patients.
Key requirements
- Completed doctorate in organic chemistry not more than 3 years ago
- Broad knowledge and practical experience in the synthesis chemistry of complex organic molecules and solid basic knowledge in physical chemistry.
- Knowledge of lipid chemistry, peptide chemistry or related specialties is advantageous
- Ability to critically evaluate scientific literature and independently develop new synthetic pathways
- Proven ability to independently identify, analyze and pragmatically solve complex synthesis and cleaning problems
- Scientific curiosity with hands-on mentality and pleasure in independent experimental work
- Enjoying practical laboratory work, as well as carrying out syntheses, processing and purification on a 10-100 g scale
- Good analytical knowledge, especially in NMR, HPLC and LC-MS and interpretation of analytical data sets.
- Experience with CAD detectors is an advantage
- High degree of initiative and the ability to drive development projects largely independently
- Excellent analytical thinking skills and quick comprehension
- Careful documentation of experiments, independent preparation of technical reports
What the company offers
- We strive for excellence in supporting this network and are committed to providing the highest quality products for the benefit of patients.
Application process
- Subordinated directly to Team Leader Lipid Development, you will be responsible for the development and practical implementation of the synthesis of novel lipids and related molecular classes to expand our lipid portfolio for pharmaceutical applications.
- Independent development of novel lipids and related molecular classes from route finding to synthesis and process development to chromatographic purification (MPLC, preparative HPLC), isolation and scaling on a 10-100 g scale
- Close cooperation with all departments involved for the successful implementation of development projects
- Introducing new, creative synthesis methods and concepts;
- Participation in scientific cooperation with external partners is desired
- Responsible for the timely preparation of all necessary documentation (technical production and status reports, etc.)
- Communication of all technical aspects to internal stakeholders.
Company and context
- CordenPharma is one of the leading Contract Development and Manufacturing Organizations (CDMO) and develops and produces pharmaceutical active ingredients, drugs and related packaging services on behalf of its customers as a “full-service” service provider.
- The group employs around 3,500 people.
- Our network in Europe, Asia and the USA offers flexible and specialized solutions for six technology platforms: Peptides, Lipids & Carbohydrates, Injectables, Highly Potent & Oncology, Small Molecules and Oligonucleotides.
- Our People Vision: We strive for excellence.
- We share our passion.
- Together, we make a difference in patients’ lives.
- Innovation Scientist (Postdoc, Chemist), 100% (m/f/d) Duration 12 months with possibility of extension. Liestal By agreement Full time
- 1 year temporary
- Your exciting task area We are looking for a committed and research-strong personality with a strong hands-on mentality.
Additional details
- Innovation Scientist (Postdoc, Chemist), 100% (m/f/d) Duration 12 months with possibility of extension.
Notes and original content
- By agreement
- Your profile
Questions about this listing
What salary does CordenPharma offer for this role?
CordenPharma lists CHF 83'000 - 138'500 gross per year for this position in Liestal. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does CordenPharma offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with CordenPharma during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Basel?
EU/EFTA residents living in the border zone of the country adjoining Canton Basel can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Basel's cantonal migration office or with HR during the application.
How do I apply for this position at CordenPharma?
Use the "Apply now" button on this page — it links directly to CordenPharma's original listing at career.cordenpharma.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
