Senior Quality Assurance Specialist – One Year Contract

Role Overview

• Ensure Distribution & In-Market Quality processes remain compliant with applicable GDP, GMP, Medical Device regulations
• Support the deployment and implementation of new or revised Quality Management System (QMS) policies, procedures, and standards
• Help identify, drive, and implement continuous improvement initiatives that enhance quality performance and operational efficiency
• Support management reviews and governance forums, including Quality Council and QMS Council activities
• Monitor regulatory developments and industry trends impacting pharmaceutical importation, distribution, and in-market quality activities

Requirements

• Bachelor or Masters Degree in Chemistry, Pharmacy, Biology, Microbiology, Chemical Engineering (or equivalent)
• Solid knowledge of global cGDPs/GMPs and Medical Device Regulations relevant to Marketing Authorization Holders
• Minimum of 5 years' experience in the pharmaceutical industry, with solid compliance experience
• Strong compliance mindset, excellent project management and organizational skills
• Good problem solving skills, based on science, facts, data, and understanding of regulatory requirements in complex and evolving environments
• Ability to work collaboratively in team settings and across functions
• Strong demonstrated interpersonal, communication, collaborative and leadership skills

Benefits

• Health insurance
• 401(k) retirement plan
• Paid time off
• Professional development opportunities
• Flexible work arrangements