The position will also responsible for supporting the scientists in R&D to prepare the documentation as required by clients, including follow up of change controls, maintaining the templates for laboratory documents.
Possuir disponibilidade para residir em : Canadá, Ontario, Mississauga.
Must be able to communicate clearly in English and have solid communication skills including grammar and composition.
Demonstrated understanding of cGMP regulations.
Proven time management skills and a strong attention to detail.
Proven ability to manage and coordinate multiple projects in a fast-paced, highly professional environment.
Proficient in using various types of computer software (Word, Excel, etc.).
Ability to work well with others and independently.
Able to read, understand and follow work instructions in a safe, accurate and timely manner.
Extended hours and shift work may be required from time to time.
Ensures full compliance with the company’s Health & Safety, Code of Integrity, and Professional Conduct policies.
Bachelor’s or Master’s degree in Chemistry or a related science degree and two or more years related pharmaceutical experience.