Associate, Regulatory Services

Found in: Jooble CA O C2 - 2 weeks ago


Mississauga ON, Canada Pharma Medica Research Inc. Full time

Pharma Medica Research is a full service Contract Research Organization specialized in conducting early phase clinical trials in healthy volunteers, special and patient populations. Currently we are looking for a Computer System Validation (CSV) Associate to join our team
The Computer System Validation Associate I is responsible for performing Pharma Medica Research Inc. ( PMRI ) computer system validation (CSV) activities as well as FDA 21 CFR Part 11 initiatives. The Computer System Validation Associate I reports to the Manager, QACA and/or designate

Validate new and existing computerized systems for compliance with company SOPs, validation program, and related regulatory requirements.
Perform GxP Computer System Change Control procedures.
Develop User Requirements, Test Cases, and Traceability Matrix.
Perform GxP and Risk Assessments.
Assist Senior CSV personnel in the implementation and maintenance of FDA 21 CFR Part 11 and related validation and regulatory requirement activities.
3+ years working experience in a related field (i.e., Excellent communication skills including excellent English verbal and written skills
~ A benefit plan that is fully paid for by PMRI, including healthcare, dentalcare, vision care, LTD, Life Insurance, AD&D, along with a Health Spending and Wellness Spending Accounts and a voluntary RRSP Contribution Plan
Corporate Discounts Program



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