Laboratory QC / IPC 100%, (m/f/d) — CordenPharma
- Location
- Liestal
- Contract
- full-time
- Posted
- 11 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 US offers flexible and specialized solutions across 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. Laborant QC / IPC 100%, (m/f/d) specialization in chemistry - in the field of quality control & in-process control
- Liestal
- immediately or by agreement
- Full time
- Perpetual
Your exciting task area
- Carrying out in-process controls (IPC) in accordance with applicable test regulations and test methods
- Support for release analyses of raw materials, intermediate and final products in accordance with applicable testing regulations and test methods
- Evaluation, documentation and evaluation of analytical results in compliance with GMP requirements
- Performance of purity tests at installations
Your profile
- Completed training as a laboratory specialist in chemistry or comparable training
- At least 2 years of professional experience in the analytical laboratory, ideally in the GMP-regulated pharmaceutical environment
- Experience with HPLC, GC, DC, spectroscopic methods and titrations
- Ideally experience with Chromeleon software
- Good knowledge of GMP guidelines
- Very good knowledge of German
- Independent, structured and solution-oriented working method
- Willingness to work flexible hours (production support)
Attractive and performance-oriented compensation package An attractive workplace with a high level of responsibility for cost sharing public transport Short distances and direct communication with all departments Corden Pharma offers you interesting and versatile tasks in a highly motivated team. Through practice-oriented training, we help you quickly gain professional security in order to work independently with a high level of personal responsibility.
- Completed training as a laboratory specialist in chemistry or comparable training
- At least 2 years of professional experience in the analytical laboratory, ideally in the GMP-regulated pharmaceutical environment
- 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 training as a laboratory specialist in chemistry or comparable training
- At least 2 years of professional experience in the analytical laboratory, ideally in the GMP-regulated pharmaceutical environment
- Experience with HPLC, GC, DC, spectroscopic methods and titrations
- Ideally experience with Chromeleon software Good knowledge of GMP guidelines Very good knowledge of German
- Independent, structured and solution-oriented working method
- Willingness to work flexible hours (production support)
- Attractive and performance-oriented compensation package An attractive workplace with a high level of responsibility for cost sharing public transport Short distances and direct communication with all departments Corden Pharma offers you interesting and versatile tasks in a highly motivated team.
- Through practice-oriented training, we help you quickly gain professional security in order to work independently with a high level of personal responsibility.
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.
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 US offers flexible and specialized solutions across 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.
- Laborant QC / IPC 100%, (m/f/d) specialization in chemistry - in the field of quality control & in-process control Liestal immediately or by agreement Full time Perpetual Your exciting task area
- Carrying out in-process controls (IPC) in accordance with applicable test regulations and test methods
- Support for release analyses of raw materials, intermediate and final products in accordance with applicable testing regulations and test methods
- Evaluation, documentation and evaluation of analytical results in compliance with GMP requirements
Additional details
- Laborant QC / IPC 100%, (m/f/d) specialization in chemistry - in the field of quality control & in-process control immediately or by agreement Your exciting task area
- Ideally experience with Chromeleon software Good knowledge of GMP guidelines Very good knowledge of German
Notes and original content
- Laborant QC / IPC 100%, (m/f/d) specialization in chemistry - in the field of quality control & in-process control
- immediately or by agreement
- Your exciting task area
- Your profile
- Ideally experience with Chromeleon software
- Good knowledge of GMP guidelines
- Very good knowledge of German
Questions about this listing
What salary does CordenPharma offer for this role?
CordenPharma lists CHF 62'000 - 94'000 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.
