6 month contract position - short notice start - valid work permit for Switzerland mandatory 

QA Ops / QA Manufacturing / Deviation Manager

BioTalent is supporting a leading biotech manufacturing facility. We need a 2-5 years experienced QA professional who is exceptional at Deviation Management to own and investigate deviations. This role involves root cause analysis, defining CAPA solutions, and ensuring cGMP compliance while collaborating with SMEs and key stakeholders.

Key Responsibilities:

• Investigate deviations, determine root causes, and implement CAPAs
• Utilize structured problem-solving tools (e.g., Fishbone, Fault Tree Analysis)
• Ensure compliance with cGMP regulations and timely closure of records
• Drive process improvements and risk management initiatives
• Work cross-functionally, influencing without formal authority

Key Requirements:

• Degree in life sciences, chemistry, biotechnology, or related field
• Experience in deviation management, cGMP, and biotech/pharma manufacturing
• Strong technical writing and communication skills
• Knowledge of risk management and process improvement is an advantage
• Fluency in English (German is a plus)