This pharmaceutical consultant role focuses on applying your GMP knowledge and experience to various projects, such that the client is confident in the approach and timing of execution of the project. Our consultants work independently within a team environment to ensure activities are undertaken in a timely manner. This position may require onsite consultant engagements within the pharmaceutical industry.
We are looking for consultants who want to apply their in-depth quality and compliance knowledge and out-of-the-box thinking to challenging projects with our clients. Our projects cover, but are not limited to: deviation investigations, change controls, CAPA, auditing, management of quality systems, delivering of training, batch document review, product releases, related to the importation of pharmaceuticals, biologics, NHPs and Medical Devices. The successful candidate would be placed in the GMP Consulting operational team who support various quality consulting roles including importing projects.
In this broad-based role, you will support the projects assigned to you, meeting the client’s needs. The role specifically prioritizes, plans, organizes and executes projects related to quality and compliance of health products to ensure smooth implementations. The role may involve coordinating/working with client personnel to meet project goals.
Reporting to the VP Consulting Services, the Lead/Senior Consultant is responsible for:
Establishing project plans that capture all aspects of the scope of work
Prioritizing and managing compliance projects
Completing critical assessments of data and documents to identify gaps compared to regulatory requirements
Communicating project milestones on a monthly basis
Completing client assigned tasks: deviation investigations, management of quality systems, review of documentation
Developing documentation as required by the project: SOPs, protocols, reports, etc.
Conducting audits both internal and external
Releasing product to market
Hosting Health Canada audits
If you are a Quality Assurance professional in the Pharmaceutical industry with at least 4-7 years experience, we have the environment and exposure to the type of work you want to do.
Education - Bachelors' degree required
Experience in the following is required:
Importation
Change Management
Deviation investigations
Master manufacturing/batch record review and lot release
Annual Product Quality Reviews
Stability review and assessment
Learn about what makes our company unique at www.qualityandcompliance.com.
Q&C welcomes and encourages applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process
