Analytical Associate

ITech Consult AG; Basel; Vor Ort; CHF 90.000 - 130.000; Vollzeit

Zusammenfassung

ITech Consult AG seeks an Analytical Associate in Analytical Development for Synthetic Molecules in Basel. The role focuses on developing and optimizing analytical methods (HPLC, GC, LC-MS) to support API quality assessment and regulatory filings.

Collaboration with process development and QC is essential, with a strong emphasis on precise scientific reporting and a proactive, independent mindset. The ideal candidate holds a chemistry/biochemistry degree or related lab training with 2–3 years in

Qualifikationen

• Completed vocational training in natural sciences or a Bachelor's degree in Chemistry/Biochemistry with 2–3 years pharma experience.
• Solid hands-on experience with analytical instruments (HPLC, GC, KF, MS) and method development.
• Strong scientific writing skills and precise reporting for regulatory filings.

Aufgaben

• Develop and optimize analytical methods (HPLC, GC, LC-MS) for quality assessment of starting materials, intermediates, and APIs.
• Plan and execute experiments, monitor reactions, and develop robust methods.
• Collaborate with process development and cross-functional teams to coordinate analytics and sample management.
• Coordinate with QC to transfer developed methods smoothly.
• Create high-quality documentation such as procedures and reports for validations and filings.
• Apply innovative digital tools to continuously improve analytical workflows.

Kenntnisse

Analytical skills

Scientific writing

Attention to detail

Bilingual EN/DE

Ausbildung

Bachelor's degree in Chemistry or Biochemistry

Laboratory Technician training

Tools

HPLC

GC

KF

MS

Jobbeschreibung

Analytical Associate in Analytical Development for Synthetic Molecules - English / Analytical instruments

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) specialises 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

The ideal candidate 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.

Tasks & Responsibilities

• Development and optimization of robust analytical methods (e.g., HPLC, GC, LCMS, 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.

Must Haves

• 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.

Nice to have

• Knowledge of GxP requirements and method validation is an advantage.

Reference Nr.: 925263SBI
Role: Analytical Associate in Analytical Development for Synthetic Molecules
Industrie: Pharma
Workplace: Basel
Pensum: 100%
Start: 01.11.-01.12.2026
Duration: 1 year++
Deadline: 01.10.2026