PROFIL ATTENDU: • BS/MS in Engineering, Life Sciences, or related technical discipline, or equivalent experience.
• 5–8 years' experience in pharmaceutical operations, QA, validation, packaging, or related areas (Oral Solid Dosage experience preferred).
• Strong knowledge of pharmaceutical manufacturing, laboratory systems, and cGxP regulations (EU-GMP, 21 CFR 210/211/Part 11, Annex 11, GAMP).
• Experience with Health Authority inspections is a plus.
• Excellent analytical, problem-solving, and project management skills.
• Strong technical writing and communication skills; ability to work across functions and levels.
• Ability to manage multiple priorities under tight deadlines.
• Fluent in English and French.