Join Bimeda as a Method Development Chemist in Cambridge, ON! This full-time role emphasizes analytical procedure development and validation for global product registrations.
Ideal candidates will have five-plus years in drug development, specifically handling microbiological methods in compliance with GMP standards. You will lead critical projects, ensuring on-time completion and regulatory adherence while providing expertise in method improvements. Your analytical skills will play a vital role in stability studies and regulatory documentation preparation.
Key Responsibilities:
• Create analytical procedures for product validation
• Maintain compliance with Good Manufacturing Practices
• Develop project timelines and write supporting reports
• Conduct stability studies and review analytical results
• Collaborate with teams on product development projects
Requirements:
• At least 5 years' experience in a related field
• B.Sc. in Chemistry or equivalent
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