Pharmaceutical Quality Compliance Specialist
7 days ago
Company Overview:
Q&C is a leading consulting firm specializing in quality and compliance services for the pharmaceutical industry.
We offer a unique opportunity to work with experienced professionals who share your passion for delivering exceptional results.
Salary:$120,000 - $150,000 per year, depending on experience.
Job Description:
This role involves applying your GMP knowledge and experience to various projects, ensuring client confidence in our approach and timing of execution. You will work independently within a team environment, prioritizing activities to ensure timely completion.
Our consultants work on challenging projects covering deviation investigations, change controls, CAPA, auditing, management of quality systems, training delivery, batch document review, product releases, and more.
You will support the GMP Consulting operational team, working closely with quality consulting roles to deliver high-quality projects.
Responsibilities:
- Establish project plans capturing all scope of work aspects
- Prioritize and manage compliance projects
- Conduct critical assessments of data and documents to identify gaps compared to regulatory requirements
- Communicate project milestones on a monthly basis
- Complete client-assigned tasks: deviation investigations, quality system management, documentation review
- Develop required documentation: SOPs, protocols, reports
- Conduct internal and external audits
- Release products to market
- Host Health Canada audits
Requirements:
- Bachelor's degree required
- At least 4-7 years of experience in the pharmaceutical industry
- Experience in importation, change management, deviation investigations, master manufacturing/batch record review, and lot release
- Annual Product Quality Reviews and stability review and assessment
Benefits:
We welcome and encourage applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process.
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