Quality Systems Associate *URGENT HIRING* Job Vacancy in Sterimax Inc. Oakville, ON – Latest Jobs in Oakville, ON

Are you looking for a New Job or Looking for better opportunities?
We got a New Job Opening for

Full Details :
Company Name :
Sterimax Inc.
Location : Oakville, ON
Position : Quality Systems Associate *URGENT HIRING*

Job Description : SteriMax Inc. is looking for a Quality Systems Associate for our growing Quality Department.The Associate, Quality Systems is responsible for supporting the Quality Systems program to align with Health Canada and FDA requirements. This position acts to maintain the APQR program, and review artwork for regulatory submissions.Principal Duties and Responsibilities: · Create, revise, and review Annual Product Quality Reviews· Compile, analyse, and interpret product quality data to evaluate trends· Review and approve artwork for printed packaging components· Generate, process, and analyse data to support Quality Systems metrics· Create, revise, and review Quality Systems documentation such as Standard Operating Procedures and material specifications· Conduct internal cGMP audits and assist in writing a detailed report· Support storage, archival, and retention of master documents· Support QA Product Release and QA Compliance activities as required· Maintain the site training program and assist in training employees as required· Support product launch activities for the Canadian and US markets as required· Implement process improvements to enhance Quality Systems· Work with cross-departmental teams to promote quality across the business· Other duties as requiredJob Requirements: · Minimum bachelor’s degree in science (Chemistry or Life Sciences) or equivalent experience· 3-5 years of practical experience in the pharmaceutical industry in Quality· Experience working in a pharmaceutical quality systems environment (i.e., APQRs, deviations, CAPA, Change Control, SOP’s etc.)· Experience reviewing and approving artwork proofs for regulatory submissions· Experience with Good Documentation Practices and Canadian GMP’s and Quality Systems; experience with US FDA cGMP’s an asset· Effective oral and written communication skills with the ability to articulate messages and interact with a variety of audiences (internal/external)· Good organizational skills, details oriented, and multi-tasking ability combined with strong attention to detailSteriMax is an equal opportunity employer that is committed to fair and accessible employment practices for all existing staff and potential candidates. Please advise Human Resources if you require an accommodation to participate in the recruitment processAGENCY NOTICE: Please note that SteriMax does not accept unsolicited resumes from recruiters or employment agencies unless we invite in writing selected recruitment agencies to participate in specifically named recruitment projects. SteriMax will not consider any referrals or agree to payment of referral or recruitment fees. In the event, a recruiter or an agency submits a resume or candidate without a previously signed agreement and a written invitation, SteriMax explicitly reserves the right to pursue and hire those candidate(s) without any financial obligation to the recruiter or agency.Job Types: Full-time, PermanentSalary: From $58,000.00 per yearBenefits:Dental careEmployee assistance programExtended health careOn-site parkingPaid time offRRSP matchSchedule:8 hour shiftApplication question(s):How many years of experience in pharmaceutical industry in Quality?Experience:APQR (Annual Product Quality Reviews): 1 year (required)Application deadline: 2022-03-19

This post is listed Under Jobs in General Category

Disclaimer : Hugeshout works to publish latest job info only and is no where responsible for any errors. Users must Research on their own before joining any company

Similar Posts