JOB OBJECTIVES Provide support to the Production department through: Monitoring and documenting events and incidents to assess their impact on product quality.
Conducting investigations: data collection, verification, analysis, and report writing. 2.
PRIMARY FUNCTIONS Initiate, investigate, and close deviations within deadlines and in accordance with corporate procedures. Lead investigations and write incident and complaint reports. Assess trends in collaboration with the Quality Assurance team. Coordinate corrective actions related to incidents and organize meetings when necessary.
Other
Participate, as needed, in drafting and updating the department’s Standard Operating Procedures (SOPs). Ensure compliance with health and safety rules (handling, behavior, etc.). Perform any other related duties deemed relevant to the position. 3.
EXPERIENCE REQUIREMENT AND APTITUDES Bachelor’s degree in science or any other relevant education. Minimum of 3 years of experience in a similar position, preferably in the sterile pharmaceutical industry. Knowledge of Canadian and international Good Manufacturing Practices (GMP).
Bilingual (French and English) with excellent written and verbal communication skills. Proficiency in computer tools, particularly the Microsoft Office suite. Strong analytical and synthesis skills, sound judgment, and problem-solving abilities.
Experience in technical writing. Team spirit. Dynamism, rigor, autonomy, and attention to detail. Robust organizational skills and ability to manage priorities. Ability to work under pressure and meet tight deadlines.