Currently 7 open positions meeting these criteria.

QA Specialist (m/f/d)

We are seeking an experienced Drug Product Quality Assurance professional to join our team and support GMP-compliant manufacturing operations. In this role, you will act as a key QA representative within cross-functional project teams, ensuring quality oversight throughout the drug product lifecycle. You will serve as a primary point of contact for quality-related topics, regulatory interactions, and continuous improvement initiatives, contributing to the maintenance and further development of an effective Quality Management System.

Process Data Scientist (m/f/d)

We are looking for a dedicated Junior Process Data Scientist to join our Drug Substance Manufacturing unit in Basel. You will focus on the core technical aspects of Multivariate Data Analysis developing validating and maintaining robust models that contribute to our quality assurance.

Global MSAT QMS Specialist (m/f/d)

Are you familiar with Quality Systems and GMP operations within the pharmaceutical industry? Then this exciting opportunity is for you!

Quality Assurance Manager Drug Product (m/f/d)

As part of the Synthetic Molecules IMP Quality Group, the QA Manager plays a key role in ensuring robust quality oversight for Synthetic Molecules Drug Substance and Drug Product operations, including associated quality control activities. Embedded within the IMP Quality Organisation Switzerland, this position is responsible for safeguarding GMP compliance and driving continuous quality improvement at the Drug Product IMP manufacturing facility at the Basel site.

The ideal candidate holds a Master’s degree in a scientific discipline and brings over 10 years of experience in the pharmaceutical industry, including a minimum of 5 years in Quality Assurance. A strong understanding of cGMP requirements and quality standards across clinical development phases is essential, along with a proven track record of successfully supporting regulatory inspections.

Fluency in both German and English is mandatory

Scientist (m/f/d)

The Manufacturing Analytics team is responsible for process analytics during the production of chemically synthesized Active Pharmaceutical Ingredients (APIs). This includes reaction monitoring and analysis of isolated intermediates in strict compliance with cGMP, safety, and regulatory requirements.

We are looking for a motivated, hands-on analytical specialist to actively contribute to a wide range of challenging and meaningful tasks within a GMP manufacturing environment.

Expert Microbiology in Quality Control (m/f/d)

As a QC Microbiology Expert, you will contribute your in-depth microbiological expertise while driving cross-functional and cross-site initiatives across the organization. You will be part of a self-organized team of microbiology specialists and collaborate closely with a broad network of internal stakeholders, including manufacturing operations, quality assurance, regulatory affairs, research and development, and global functions.

The ideal candidate is open-minded and curious, willing to challenge established ways of thinking and to contribute new perspectives. You thrive in a performance-driven environment built on mutual respect, open dialogue, and collaboration. You are a confident and communicative professional who enjoys working independently while acting as a key interface between different functions. With strong prioritization skills, you proactively identify opportunities for improvement and initiate effective optimization measures. You maintain a holistic view, work with precision, and demonstrate a high level of quality awareness in a regulated GMP environment.

Senior Medical Director, Clinical Development (m/f/d)

As Senior Medical Director, Clinical Development you will be a key member of the interdisciplinary development team, contributing effectively and independently to clinical development of assigned assets. This is a high visibility leadership role directly reporting to the Head of Clinical Development, Basel Site. You will lead clinical development activities relating to the design, execution, and interpretation of clinical trials and the clinical development plan. You will work with the study management teams, training internal and external staff, monitoring clinical data, and responding to health authority requests related to the assigned clinical development activities.

The successful candidate will integrate clinical and research expertise with leadership skills to advance clinical development strategy