Elevate compliance in manufacturing with your expertise as a Manufacturing Compliance Specialist. Focus on deviations and root-cause analysis in a dynamic pharmaceutical environment.
We seek a dedicated Manufacturing Compliance Specialist with a university degree in a related science. Candidates should have at least 3 years of experience in the pharmaceutical sector, showcasing proficiency in root cause analysis, project management, and corrective action tools. Excellent technical writing skills and superior organizational abilities are vital for effective communication across functions.
Key Responsibilities:
- Conduct investigations following established procedures
- Identify critical paths for timely root cause identification
- Facilitate teams to analyze deviations and solutions
- Write and review investigation reports for accuracy
- Manage corrective actions and prepare recommendations
Requirements:
- University degree in a related science field
- Minimum 3 years in pharmaceutical Quality Assurance
- Strong skills in technical writing and communication
- Knowledge of GMP standards and ERP systems
- Critical thinking and problem-solving abilities
Harness your compliance expertise and drive excellence in manufacturing.
Manufacturing Compliance Specialist Needed in Cambridge employer: Septodont
Duoject, located in Bromont, Quebec, is an exceptional employer that prioritizes employee development and well-being. With a collaborative work culture, competitive compensation, and a strong focus on innovation in the medical device industry, employees have the opportunity to work on cutting-edge projects while enjoying benefits such as financial support for wellness activities and professional growth programs. Joining Duoject means being part of a team that values creativity, diversity, and meaningful contributions to healthcare.
