Analytical Expert

vor 1 Tag

Basel, Schweiz Datalynx AG Vollzeit

For our client, a well-known pharmaceutical company in Basel, we are looking for an Analytical Expert (M/F/d).

**Background**

We are at the forefront of innovative therapies with 14 Radio Ligand Therapy (RLT) projects in our rapidly expanding development pipeline. As part of our Global Technical R&D team, the Analytical Research & Development (ARD) department plays a crucial role in the characterization and analysis of Small Molecule Drug Substances and Drug Products, from discovery to commercial production. We are looking for a highly motivated Analytical Expert to join our team and contribute to the success of our RLT projects.

**General Information**:

- Start date: 01.01.2025
- Duration: 12 month
- Extension: Possible
- Workload: 100%
- Work location: Basel

**Tasks & Responsibilities**:

- Plan, interpret, and report on scientific experiments to ensure timely delivery of drug substances (DS) and drug products (DP)
- Write and review key analytical documents, including methods, specifications, validation reports, stability reports, and batch records for stability and release testing, while coordinating global project activities
- Manage relationships with internal and external stakeholders, providing scientific and technical guidance on outsourced activities as needed
- Proactively identify challenges in science, technology, and GMP; propose innovative solutions and communicate issues to the Analytical Project Leader or technical team
- Adhere to SOPs, GMP standards, Quality Directives, and Health and Safety guidelines
- Contribute to analytical CMC documents and support regulatory submissions
- Drive and manage analytical activities related to RLT compounds, including impurity profiling, method development, validation, stability, and release testing
- Provide scientific guidance to cross-functional and global project teams to advance our RLT portfolio
- Foster a collaborative, positive attitude with project teams, stakeholders, and partners

**Must Haves**:

- PhD or Master’s degree in Analytical Chemistry or related field
- Minimum of 2-4 years in the pharmaceutical industry with proven experience in GMP activities for development or marketed products
- Expertise in analytical raw data documentation and technical writing (e.g., stability reports, validation).
- Strong scientific knowledge in chemistry, pharmaceutical sciences, and analytical methods
- Advanced proficiency in laboratory tools and technical systems (e.g., HPLC, LC-MS, Quality Management Systems, statistical tools)
- Skilled in scientific/technical writing and proficient with standard software and computer tools
- Demonstrated leadership in mentoring and guiding colleagues
- Strong coordination skills, collaborative spirit, proactive approach, and eagerness to learn
- High level of quality focus and effective communication skills
- Fluent in English (oral and written)

**Nice to Have**
**- Pharmaceutical background

**Contact**:
Jan Schmitz-Elsen
Team Lead Talent Acquisition
+41 79 425 10 45

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