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QA Specialist - A/QPIC
Job in
Richmond, BC, Canada
Listed on 2026-07-10
Listing for:
Medisca
Full Time
position Listed on 2026-07-10
Job specializations:
-
Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, Quality Engineering, QA Specialist - Analyst/Manager, Data Analyst
Job Description & How to Apply Below
The primary purpose of the A/QPIC – QA Specialist is to fulfill day-to-day activities involving controlled substances as well as quality assurance. The position performs activities involving narcotics and controlled substances in terms of receiving, inventory, shipping, and reporting to ensure compliance with controlled substance regulations. The position also handles Quality Events, Quarantines, Rejections, Returns, and other Quality Assurance-related activities to ensure compliance with GMP.
This individual is expected to work in a team environment and independently to meet defined objectives based on established timelines and deliver project work in a manner consistent with the company’s values.
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!
Location
Richmond, BC - Onsite
Hours
8:30am - 5:00pm Monday - Thursday, 8:30am - 3:45pm Friday
Salary
$60,000 annually
The opportunity
We invest time and resources into making sure Medisca is as good as the people we hire.
Responsibilities & Duties
Controlled Substance Activities
Process Outbound Controlled Substance orders as per SOP
Verify and process order information
Pick and pack the correct product with accuracy
Select appropriate courier and ship the order with accuracy
File and retain relevant documents
Process Inbound Controlled Substance orders as per SOP
Review and initiate replenishment orders for Controlled Substances
Inspect incoming packages of Controlled Substances for damage or tampering
Verify the goods to ensure accurate identity and quantity against the original order sheet
Maintain Inventory and Reports
Perform monthly and year-end inventory count of Controlled Substances
Prepare monthly activity reports of Controlled Substances
Prepare Loss and Theft reports (when applicable)
Complete periodic security checks
Quality Control / Quality Assurance
Collaborate and ensure adequacy of SOPs and Quality-related documentation
Initiate Quality Events as per SOPs to ensure compliance with GMP and regulations
Perform Quality functions such as Quarantine, Rejection, Inspection to assist in investigations
Maintain system information such as Code set-ups, BOMs, specs, etc
Support calibration and monitoring activities of the Temperature/Humidity Environmental Monitoring System
Support validation activities, as applicable
Qualifications
Minimum B.S. Degree or equivalent in Life-science or related field
Previous designation/experience as QPIC or A/QPIC is considered an asset
Experience in a cGMP environment is considered an asset
Working knowledge of regulations required (cGMP, 21 CFR PART 11 and 211, ICH Q7, GUI 0104, GAMP 5, NCR)
Experience with quality systems including change control, risk assessment and management, incident management, and deviation management
Strong attention to detail as well as analytical & problem solving skills
Self-motivated and quick learner of processes and technologies
Ability to multitask and manage/prioritize multiple projects and deadlines with high accuracy
Excellent technical writing and communication skills
Able to work well both independently and collaborate with others
Knowledge of Microsoft Office (Word, Excel), Syspro and Master Control is considered an asset
Excellent communication skills; fluent English (oral & written) required
What’s In It For You…
Work/Life Balance - PTO and vacation policy
Invest in your health – Choice of modular plans, health spending account and free Telemedicine
Your Future is Bright – Opportunities to learn and grow within Medisca
Save for your Future – Medisca contributes to a deferred profit sharing plan (DPSP) when you invest in RRSPs
Help us grow – Employee Referral Program
We like to have fun – company events throughout the year
We thank all applicants for their interest; however, only candidates to be interviewed will be contacted.
We are an equal opportunity employer.
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