Specialist QC Operational Excellence (Pharmaceutical)

TL;DR

Specialist QC Operational Excellence (Pharmaceutical): Optimizing quality control processes and ensuring GMP compliance within a pharmaceutical manufacturing environment with an accent on lean principles and waste reduction. Focus on leading root cause investigations, implementing CAPAs, and driving data-driven continuous improvement strategies using Lean and Six Sigma.

Location: On-site in Switzerland

Company

hirify.global is a global pharmaceutical, biopharmaceutical, and medical device outsourcing company.

What you will do

• Manage cross-functional projects to enhance operational performance, reduce waste, and improve product quality.
• Implement data-driven continuous improvement strategies using Lean, Kaizen, and Six Sigma methodologies.
• Lead OOX and deviation investigations, performing root cause analysis and establishing effective CAPAs.
• Standardize QC project processes and optimize the training process within the QC laboratory.
• Author and review documentation, including TWIs and SOPs, to support process improvements.
• Act as a Subject Matter Expert (SME) during client audits and health authority inspections.

Requirements

• Master or PhD degree in Life Sciences, Chemistry, Pharmacy, or equivalent.
• Lean Management certification (Green Belt).
• At least 5 years of experience in continuous improvement activities in Quality Control within a pharmaceutical company.
• Thorough understanding of cGMP and regulatory requirements.
• Strong practical knowledge of analytical techniques (HPLC, UPLC, GC, dissolution, UV/Vis, Karl Fischer).
• Excellent oral and written communication skills in both French and English.

Nice to have

• Experience with OSD (Oral Solid Dosage) and/or CMO (Contract Manufacturing Organization).

Culture & Benefits

• Opportunity to play a pivotal role in fostering a culture of ongoing enhancement and continuous improvement.
• Collaboration with international peers across multiple sites.