Do you want to make a valuable contribution to patients' health and take responsibility for achieving something truly meaningful?
Then we look forward to meeting you
Excellence beyond manufacturing – this is what Aenova stands for. With 4,000 employees at 15 sites worldwide, we are one of the leading contract manufacturers and developers for the pharmaceutical industry. Our Sisseln site is a competence center for complex and innovative solid dosage forms.
Responsibilities
• Development and optimization of pharmaceutical formulations, taking technological and regulatory requirements into account
• Independent planning, execution, and evaluation of development trials as well as preparation of development documentation (protocols, reports, MBRs, formulations in the SAP system)
• Responsibility for the execution and supervision of manufacturing processes and development batches, including in-process controls and GMP-compliant documentation
• Close (daily) collaboration and regular reporting to the project manager to ensure the scientific and technological achievement of project objectives
• Close cooperation with adjacent departments (e.g., Analytical Quality Control, Production, Engineering, Procurement, Quality Assurance)
• Technological research on new excipients, processes, and platforms for the advancement of formulation approaches and technologies
• Support the implementation of new manufacturing technologies as well as continuous improvement of processes, workflows, and structures in pharmaceutical development/formulation
• Responsibility for compliance with quality, safety, and environmental standards within project work