To support our growth in Switzerland, we are looking for a consultant:
We are looking for an External Manufacturing Operations Lead Consultant to oversee and support the management of Contract Manufacturing Organizations (CMOs) involved in the production of biological drug substances.
The role ensures supply continuity by guaranteeing quality, compliance, timelines, and cost efficiency, while building strong and long-term partnerships. Responsibilities cover both clinical and commercial supply within a GMP-regulated environment.
Key Responsibilities
Oversee external production and ensure timely supply of biological drug substances.
Manage planning, budgets, KPIs, and GMP documentation to maintain compliance.
Maintain regular and effective communication with CMOs and coordinate technical issue resolution.
Contribute to long-term sourcing strategies and contractual management (MSAs, Quality Agreements, risk assessments).
Lead technical projects including tech transfers, process validations, and continuous improvement initiatives.
Draft, review, and approve regulatory and technical documentation related to manufacturing.
Master’s degree in Science, Engineering, or related field.
At least 2 years of experience in the biopharma/biotech industry, ideally in manufacturing or QA.
Knowledge of biological processes (fermentation, purification) and GMP regulations.
Experience managing outsourced activities and technical projects is a strong asset.
Strong communication, leadership, and budget management skills.
Analytical mindset with a proactive, problem-solving approach.