Medisca is a global corporation with locations throughout North America, Australia, and Europe, that contributes to healthcare by leveraging strong partnerships that deliver customized solutions with an unwavering commitment to quality and innovation. Backed by 30+ years and a strong foundation in pharmaceutical compounding, Medisca is a business-to-business company that delivers comprehensive offerings by providing value, consistency, responsiveness, and loyalty. From pharmaceutical compounding products and services, to supply chain solutions, mixing technology manufacturing, analytical testing, IP licensing, to education services and more \xe2\x80\x93 Medisca delivers extensive solutions that leverages a strong network of partners committed to deeply caring about people. As Partners in Wellness, Medisca offers an unfailing devotion to improving lives, across a multitude of needs and across a multitude of people. The main purpose of the QA Specialist position is to manage all controlled documents through MEDISCA\xe2\x80\x99s Quality Management System for all products across all facilities as well as to support maintain the company\xe2\x80\x99s stability program. If you are an enthusiastic self-starter, goal driven, love quality and have an interest in the pharmaceutical industry, then we are looking for you! The opportunity: Documentation and Customer notifications

• Create / Approve Certificates of Analysis (CofA), Product Specifications, SDS\xe2\x80\x99s and Labels according to set procedures
• Maintain the accuracy of documentation through MEDISCA\xe2\x80\x99s Quality Management System
• Collaborate with other departments for accurate anyd streamlined implementation of changes through Action Items (AI\xe2\x80\x99s) as well as timely approval of controlled documents
• Prepare change notification documents for customers
• Prepare product specific statements and documents for customers

Stability Program

• Prepare documentation required for stability studies
• Follow up with testing labs to ensure timely performance of analysis at each pull point per the approved stability protocol
• Review and maintain stability reports in MEDISCA\xe2\x80\x99s Quality Management System

Any other tasks as needed within the Quality department Required Experience:

• One (1) to three (3) years\xe2\x80\x99 experience in Quality Control and/or Quality Assurance in Pharmaceutical industry

Required Skills:

• Bachelor\xe2\x80\x99s degree in a Science related field required
• In-depth knowledge of pharmaceutical industry quality standards, regulations and guidelines
• Capable to manage multiple priorities across multiple facilities
• Accuracy of work and proofreading skills
• Excellent communication skills required; fluent English & French (oral & written). This position requires communication with customers based across Canada and the United States.
• Proactive and dedicated team player
• Good command of Microsoft Office (Word, Excel, Outlook) required

What\xe2\x80\x99s In It For You \xe2\x80\xa6 We invest time and resources into making sure Medisca is as good as the people we hire.

• Work/Life Balance - 40 hour workweek with early Fridays all year long, PTO and vacation policy
• Invest in your health \xe2\x80\x93 Choice of modular plans, health spending account and free Telemedicine
• Your Future is Bright \xe2\x80\x93 Opportunities to learn and grow within Medisca
• Save for your Future \xe2\x80\x93 Medisca contributes to a deferred profit sharing plan (DPSP) when you invest in RRSPs
• Help us grow \xe2\x80\x93 Employee Referral Program
• We like to have fun \xe2\x80\x93 company events throughout the year

We are an equal opportunity employer #LI-Onsite