Scientist

Actalent; Basel; On-site; CHF 120,000 - 160,000; Full time

Job summary

Actalent is seeking an Expert in Science & Technology to join the Analytical Research & Development team. The role focuses on characterization and analysis of Small Molecule Drug Substances and Drug Products from discovery to transfer to production, with emphasis on GMP analytics and regulatory collaboration.

Key activities include leading experiments, documenting methods, and coordinating with CROs and global project teams.

Qualifications

• Broad scientific knowledge in chemistry, pharmaceutical or analytical sciences.

Responsibilities

• Plan, organize, interpret and report results of experiments for clinical DS/DP supply.

Skills

Analytical chemistry knowledge

Presentation skills

Scientific writing

Collaboration in international env

Education

Bachelor's/Master's in Life Science

Tools

HPLC

Dissolution rate

Chromeleon

Quality management systems

Statistical evaluation tools

Job description

We are looking for a highly motivated Expert in Science & Technology to support Analytical Research & Development (ARD). ARD sits within the Global Technical R&D department of Development and plays an essential role in the characterization and analysis of Small Molecule Drug Substances and Drug Products from the time they leave the discovery laboratory until they are transferred to Commercial Production. The role will be part of the Small Molecules GMP Analytics Team with main focus on small molecules and Radioligand Therapy.

Start: 04.01.2027

18 months Contract

Major accountabilities:

• Independently plan, organize, interpret and report results of scientific experiments for timely supply of drug substances (DS) and drug products (DP) intended for clinical use and potential registration as a future commercial asset
• Write & review analytical documents (e.g Analytical methods, Specifications, Validation reports, Stability reports, Batch records for stability and release testing) and align the corresponding activities within a global CMC project team comprising of chemists, formulators, quality assurance and regulatory
• Manage interactions with internal and external stakeholders (e.g. lab analysts, analytical project leader, CMC project team), including outsourced activities to CROs by providing scientific and technical guidance whenever necessary. Support or Manage OOx/Deviations/Investigations as needed.
• Proactively identify scientific, technological and GMP challenges, proposing creative solutions and communicating key issues to the appropriate management level and respective technical project team
• End-to-end portfolio project responsibility. Represent the team in the Analytical Sub team meetings
• If required, perform and document laboratory experiments in appropriate systems (e.g. GLIMS eLN). Responsible for good documentation practices (GDP) and good laboratory practices (GLP) during execution of laboratory activities
• Support/Lead actively initiatives/workstreams as required
• Support audits and health authority inspections and ensure no critical findings within the assigned scope
• Responsible to meet KQI (Key quality indicators) and KPI (Key performance indicators) for all assigned activities.
• Actively contribute to team and organization goals
• Work according to appropriate SOPs, GMP, HSE, ISRM and Novartis Guidelines
• Bachelors/Masters in Life Science (e.g., analytical / organic chemistry /pharmacy / pharmaceutical development) or equivalent
• 3+ years of related experience in a GMP environment
• Broad scientific knowledge in chemistry, pharmaceutical or analytical sciences, ability to perform in a highly dynamic and flexible environment.
• Advanced knowledge of laboratory and/or technical tools (e.g. HPLC, Dissolution rate, Chromeleon, Quality management systems, statistical evaluation tools ...)
• Good presentation skills and scientific/technical writing skills. Strong ability to work and collaborate in an international environment