For one of our clients, an international pharmaceutical company, in the canton of Neuchâtel, we are seeking a
Bulk Manufacturing Manager
Contract: Permanent (CDI)
A unique opportunity to contribute to the manufacturing of high-quality pharmaceutical products in a stimulating and innovative environment!
Your role:
- Oversee daily Bulk team management, ensuring timely delivery.
- Develop and manage the Bulk Operations team, encompassing manufacturing, planning, and cleaning.
- Define and implement mid-term departmental strategies, including resource planning and succession planning.
- Lead corrective actions and improvement initiatives, ensuring GMP compliance and KPI attainment.
- Manage bulk operations planning aligned with logistical needs.
- Lead cross-functional projects and act as a subject matter expert.
- Propose, sponsor, and manage improvement projects.
- Support in establishing and monitoring the bulk budget.
- Ensure traceability and compliance of all operations.
- Conduct investigations into failures, develop and implement remediation plans.
- Represent Bulk Operations during health authority audits.
- Develop and maintain Standard Operating Procedures.
- Ensure compliance with quality systems and EHS directives.
Your background:
- Master's degree in a relevant scientific field.
- 5+ years' experience in pharmaceutical bulk GMP activities.
- 3+ years' experience managing GMP activities and teams.
- Strong knowledge of cGMP and relevant regulations.
- Fluency in both French and English.
- Strong leadership, communication, and decision-making skills.
- Experience with LEAN methodologies.
