Pharma Medica Research (PMRI) Inc. is a Contract Research Organization that strives for innovation and original solutions in a highly regulated and competitive industry. If your career goals align with innovation and original thinking you will be the perfect candidate to be part of an inclusive, adaptable, and forward-thinking organization. Our reputation for delivering high quality research is outstanding. At PMRI we are committed to making a difference in healthcare and people’s lives. Come join our team!
We are currently looking for a QA Associate to join our team in Mississauga, Ontario!
The QA Associate ensures compliance of activities conducted at the Pharma Medica Research Inc. (PMRI) Laboratory/Head Office location. This position reports to the Manager, QA (Corporate) and/or designate.
Duties and Responsibilities
Prepare and conduct audits of the bioanalytical and laboratory activities, data and reports for compliance with Good Laboratory Practice (GLP), PMRI Corporate policies, departmental SOPs and other regulations/guidelines as deemed appropriate.
Audit the final study report/statistics for compliance with Good Clinical Practice (GCP), PMRI Corporate policies, departmental SOPs and other applicable regulations/guidelines.
Conduct audits of the Phase 2-4 clinical trial activities for compliance with applicable GCP regulations, departmental SOPs and other applicable regulations/guidelines.
Report findings to the Principal Bioanalytical Investigator and/or applicable departmental Management; follow-up to ensure adequate completion of corrective actions.
Ensure QA management is kept up to date regarding audit findings/corrective actions.
Provide input and support as required to all PMRI divisions to ensure compliance to SOPs, GLP, GCP and other regulatory requirements.
Other duties as required
Responsibilities
B.Sc. degree, Post-Secondary Diploma in scientific, healthcare, or pharmaceutical field, or equivalent
0-3 years related experience (combined or equivalent) in a quality assurance, quality control or laboratory role
Experience with MS Office software
Good understanding of applicable Health Canada, FDA, EU, ICH GLP and GCP regulations and guidelines
Works closely with all departments and personnel to ensure PMRI’s quality objectives are achieved
Ability to work within a team environment
Very organized and able to multi-task
Meticulous with well-developed problem-solving skills
Excellent written and oral skills
We offer:
Competitive compensation plan
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
Opportunities for advancement and career progression
A generous Employee Milestones Awards Program
Corporate Discounts Program
Learning Support Programs
Friendly atmosphere, culture of learning
Please note all applications must be eligible to work within Canada.
PMRI is an Equal Opportunity Employer; promoting accessibility and inclusivity at work and offering accommodation for applicants as required and requested.
We thank all applicants for their interest; however, only those selected to proceed in the interview process will be contacted.
