Compliance Associate
Omega Laboratories Limited
Montréal, QC
Omega is offering you!

A dynamic & collaborative work team!
Growing company.
Safe working environment.
Flexibility of schedule.
Group insurance.
Group RRSP with employer contribution.
Train and public transport nearby.
What will you have to do?

Plan and do inspections of suppliers of raw materials and packaging components.
Plan and do nspections in external analytical laboratories and subcontracting companies.
Issue and follow up on inspection reports.
Evaluate the corrective action plan of the audited companies and internal audits.
Plan and carry out self-inspections covering the corresponding sections of the GMP.
Participate in activities related to inspections by company customers and regulatory authorities.
Manage annual product quality reports, ensure that information is up to date and ensure that reports are completed in the first quarter or as per customer agreements.
Write or update SOPs specific to your department.
Ensure that Quality Policies are in place with selected customers and suppliers.
Manage the database for archiving.
Periodically notify department heads of the destruction of documents in the archives.

We would like to meet you if you have :
Bachelor of Science or equivalent.
6 to 9 years' experience in quality assurance in the pharmaceutical industry.
Bilingualism (French and English) oral and written.
Excellent knowledge of GMP and Canadian and American regulations.
Ability to work in a team and good interpersonal skills.
Rigour and organization.
Ability to work under pressure and manage priorities in a dynamic environment.
Demonstrates initiative, resourcefulness and autonomy.
Analytical and synthetic mind, sense of observation and judgment.
Decision-making authority.
Effective time and priority management.

Bonus point :
Auditor certification (an asset).
We know that responding to a job offer is a lot of work and we sincerely appreciate the time you spend with us. Emilie will be happy to consider your application.