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We make it GmbH is a company operating nationally in Switzerland. Thanks to many years of successful experience, it has a high level of competence in the personnel services sector. Concentration of placement activities on the core areas of industry, technology, office/administration, engineering, pharmaceuticals and IT. We make it GmbH places the highest demands on quality, ethics and discretion. For our customer, the company F. Hofmann La Roche, are we searching for:   Analytical Associate in Analytical Development for Synthetic Molecules (m/w/d)   Background Pharma Technical Development (PTD) is a global team of over 2,000 experts dedicated to developing innovative medicines to meet patient needs. Within PTD, Synthetic Molecules Technical Development (PTDC) specializes in active pharmaceutical ingredients (APIs), drug products, and analytical sciences. PTDC plays a vital role in advancing the synthetic molecules pipeline, supporting research, early development, and clinical trials through technical innovation and collaboration. This position is located within the Analytical Development for Synthetic Molecules department, where cutting-edge techniques such as High-Performance Liquid Chromatography (HPLC), Gas/Ion Chromatography (GC/IC), and Mass Spectrometry (MS) are used to develop efficient and robust analytical methods. The goal is to ensure product release for clinical trials and subsequent commercial supply through a rigorous control strategy. Take a leading role in the development of innovative analytical techniques while contributing to the success of clinical and commercial therapies — apply now and help shape the future of healthcare! The Perfect Candidate (m/f/d) holds a vocational qualification in natural sciences or a Bachelor's degree in Chemistry or Biochemistry, combined with several years of experience in the pharmaceutical industry. They bring proven expertise in instrumental analytics—such as HPLC, GC, KF, and MS—as well as solid experience in method development. Operating with strong quality awareness and exceptional attention to detail, they excel in precise scientific writing. A proactive, independent mindset along with fluent German and good English skills round out the profile.   Work hours Standard 40h / Week   Tasks Development and optimization of robust analytical methods (e.g., HPLC, GC, LC-MS, GC-MS, KF) for the quality assessment of starting materials, intermediates, and active pharmaceutical ingredients (APIs), Planning and meticulous execution of experiments, including reaction monitoring and method development, Close collaboration with process development and cross-functional partners to coordinate analytical activities and sample management, Close cooperation with the QC (Quality Control) unit to ensure a smooth transfer of the developed analytical methods, Creation of high-quality documentation, including analytical procedures and reports that serve as the foundation for method validations and regulatory filings, Application of an innovative mindset and digital tools for continuous improvement of analytical workflows in a dynamic environment.   Qualifications Completed vocational training in natural sciences (Laboratory Technician) or a Bachelor's degree in Chemistry, Biochemistry, or a related field with at least 2-3 years of professional experience in the pharmaceutical industry. (*****), Solid practical experience with analytical instruments (e.g., HPLC, GC, KF, MS) as well as strong expertise in method development. (*****), Strong scientific writing skills and the ability to summarize and present results of complex experiments precisely. (*****), High quality awareness and uncompromising attention to detail, including work within a non-GMP development environment. (*****), Proactive, self-motivated work style and the ability to adapt quickly to new tools and processes in a dynamic team environment, Fluent English language skills (both spoken and written) and German is beneficial.   Are you interested? Then Mr. Raphael Sigg looks forward to receiving your complete application documents (CV, certificates and training certificates). We look forward to hearing from you. Please send your application by e-mail to consulting@we-make-it.ch We look forward to hearing from you
  • we make it GmbH
  • Jobs
  • We make it GmbH is a company operating nationally in Switzerland. Thanks to many years of successful experience, it has a high level of competence in the personnel services sector. Concentration of placement activities on the core areas of industry, technology, office/administration, engineering, pharmaceuticals and IT. We make it GmbH places the highest demands on quality, ethics and discretion. For our customer, the company F. Hofmann La Roche, are we searching for:   Analytical Associate in Analytical Development for Synthetic Molecules (m/w/d)   Background Pharma Technical Development (PTD) is a global team of over 2,000 experts dedicated to developing innovative medicines to meet patient needs. Within PTD, Synthetic Molecules Technical Development (PTDC) specializes in active pharmaceutical ingredients (APIs), drug products, and analytical sciences. PTDC plays a vital role in advancing the synthetic molecules pipeline, supporting research, early development, and clinical trials through technical innovation and collaboration. This position is located within the Analytical Development for Synthetic Molecules department, where cutting-edge techniques such as High-Performance Liquid Chromatography (HPLC), Gas/Ion Chromatography (GC/IC), and Mass Spectrometry (MS) are used to develop efficient and robust analytical methods. The goal is to ensure product release for clinical trials and subsequent commercial supply through a rigorous control strategy. Take a leading role in the development of innovative analytical techniques while contributing to the success of clinical and commercial therapies — apply now and help shape the future of healthcare! The Perfect Candidate (m/f/d) holds a vocational qualification in natural sciences or a Bachelor's degree in Chemistry or Biochemistry, combined with several years of experience in the pharmaceutical industry. They bring proven expertise in instrumental analytics—such as HPLC, GC, KF, and MS—as well as solid experience in method development. Operating with strong quality awareness and exceptional attention to detail, they excel in precise scientific writing. A proactive, independent mindset along with fluent German and good English skills round out the profile.   Work hours Standard 40h / Week   Tasks Development and optimization of robust analytical methods (e.g., HPLC, GC, LC-MS, GC-MS, KF) for the quality assessment of starting materials, intermediates, and active pharmaceutical ingredients (APIs), Planning and meticulous execution of experiments, including reaction monitoring and method development, Close collaboration with process development and cross-functional partners to coordinate analytical activities and sample management, Close cooperation with the QC (Quality Control) unit to ensure a smooth transfer of the developed analytical methods, Creation of high-quality documentation, including analytical procedures and reports that serve as the foundation for method validations and regulatory filings, Application of an innovative mindset and digital tools for continuous improvement of analytical workflows in a dynamic environment.   Qualifications Completed vocational training in natural sciences (Laboratory Technician) or a Bachelor's degree in Chemistry, Biochemistry, or a related field with at least 2-3 years of professional experience in the pharmaceutical industry. (*****), Solid practical experience with analytical instruments (e.g., HPLC, GC, KF, MS) as well as strong expertise in method development. (*****), Strong scientific writing skills and the ability to summarize and present results of complex experiments precisely. (*****), High quality awareness and uncompromising attention to detail, including work within a non-GMP development environment. (*****), Proactive, self-motivated work style and the ability to adapt quickly to new tools and processes in a dynamic team environment, Fluent English language skills (both spoken and written) and German is beneficial.   Are you interested? Then Mr. Raphael Sigg looks forward to receiving your complete application documents (CV, certificates and training certificates). We look forward to hearing from you. Please send your application by e-mail to consulting@we-make-it.ch We look forward to hearing from you

Analytical Associate in Analytical Development for Synthetic Molecules (m/w/d) for F. Hoffmann La Roche in Basel

Jobtitel:
Analytical Associate in Analytical Development for Synthetic Molecules (m/w/d) for F. Hoffmann La Roche in Basel
Datum:
25.09.2026
Beschreibung:

We make it GmbH is a company operating nationally in Switzerland. Thanks to many years of successful experience, it has a high level of competence in the personnel services sector. Concentration of placement activities on the core areas of industry, technology, office/administration, engineering, pharmaceuticals and IT. We make it GmbH places the highest demands on quality, ethics and discretion.

For our customer, the company F. Hofmann La Roche, are we searching for:

 

Analytical Associate in Analytical Development for Synthetic Molecules (m/w/d)

 

Background

Pharma Technical Development (PTD) is a global team of over 2,000 experts dedicated to developing innovative medicines to meet patient needs. Within PTD, Synthetic Molecules Technical Development (PTDC) specializes in active pharmaceutical ingredients (APIs), drug products, and analytical sciences. PTDC plays a vital role in advancing the synthetic molecules pipeline, supporting research, early development, and clinical trials through technical innovation and collaboration. This position is located within the Analytical Development for Synthetic Molecules department, where cutting-edge techniques such as High-Performance Liquid Chromatography (HPLC), Gas/Ion Chromatography (GC/IC), and Mass Spectrometry (MS) are used to develop efficient and robust analytical methods. The goal is to ensure product release for clinical trials and subsequent commercial supply through a rigorous control strategy. Take a leading role in the development of innovative analytical techniques while contributing to the success of clinical and commercial therapies — apply now and help shape the future of healthcare!

The Perfect Candidate (m/f/d) holds a vocational qualification in natural sciences or a Bachelor's degree in Chemistry or Biochemistry, combined with several years of experience in the pharmaceutical industry. They bring proven expertise in instrumental analytics—such as HPLC, GC, KF, and MS—as well as solid experience in method development. Operating with strong quality awareness and exceptional attention to detail, they excel in precise scientific writing. A proactive, independent mindset along with fluent German and good English skills round out the profile.

 

Work hours

Standard 40h / Week

 

Tasks

Development and optimization of robust analytical methods (e.g., HPLC, GC, LC-MS, GC-MS, KF) for the quality assessment of starting materials, intermediates, and active pharmaceutical ingredients (APIs), Planning and meticulous execution of experiments, including reaction monitoring and method development, Close collaboration with process development and cross-functional partners to coordinate analytical activities and sample management, Close cooperation with the QC (Quality Control) unit to ensure a smooth transfer of the developed analytical methods, Creation of high-quality documentation, including analytical procedures and reports that serve as the foundation for method validations and regulatory filings, Application of an innovative mindset and digital tools for continuous improvement of analytical workflows in a dynamic environment.

 

Qualifications

Completed vocational training in natural sciences (Laboratory Technician) or a Bachelor's degree in Chemistry, Biochemistry, or a related field with at least 2-3 years of professional experience in the pharmaceutical industry. (*****), Solid practical experience with analytical instruments (e.g., HPLC, GC, KF, MS) as well as strong expertise in method development. (*****), Strong scientific writing skills and the ability to summarize and present results of complex experiments precisely. (*****), High quality awareness and uncompromising attention to detail, including work within a non-GMP development environment. (*****), Proactive, self-motivated work style and the ability to adapt quickly to new tools and processes in a dynamic team environment, Fluent English language skills (both spoken and written) and German is beneficial.

 

Are you interested?

Then Mr. Raphael Sigg looks forward to receiving your complete application documents (CV, certificates and training certificates). We look forward to hearing from you.

Please send your application by e-mail to consulting@we-make-it.ch

We look forward to hearing from you

Region:
Basel
Kategorie:
Labor & Qualität
Branche:
Chemie/Pharma

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