Novartis AG

Associate Expert Drug Supply

📍 Basel (City)

Role and responsibilities

Manufacture solid dosage forms in compliance with Good Manufacturing Practice standards. Sieving and milling of active pharmaceutical ingredients. Perform in-process (IPC) and process flow controls (PAK), ensuring accurate documentation within manufacturing execution systems. Execute encapsulation, tableting, granulation, and precise drug processing (PDP) activities according to approved procedures. Operate, set up, clean, and disinfect manufacturing equipment and production areas. Support equipment maintenance, calibration, qualification, and commissioning activities. Contribute to audit readiness, continuous improvement initiatives, and key performance indicator achievement. Collaboration in the creation / revision of procedural documents (SOP, WP, FRM). Ensure compliance with quality, safety, data integrity, and information security requirements.

Team / description

Joining our TRD PHAD Oral Supply team, you will work in a highly collaborative and quality-focused environment where your expertise directly contributes to the development of new treatments and helps transform patients’ lives.

Qualifications and Skills

  • Completed vocational training in a technical, pharmaceutical, chemical, food production, or related field.

  • Fluent German language skills, both written and spoken.

  • Good English language skills, both written and spoken.

  • Experience working within a Good Manufacturing Practice regulated environment.

  • Hands-on experience operating manufacturing equipment and following documented procedures.

  • Knowledge of pharmaceutical manufacturing processes, including active ingredients or solid dosage forms.

  • Strong commitment to quality, safety, compliance, and continuous improvement.