Manufacturing Quality Assurance Associate - Night

at  Deciem

WHAT ON EARTH IS DECIEM?

Known as “The Abnormal Beauty Company”, DECIEM is the parent company of The Ordinary, NIOD, and other beauty brands & is an industry disruptor with a science first approach to innovation. DECIEM was Co-Founded in 2013 by the late Brandon Truaxe, a visionary who set out to change the beauty industry through authenticity and transparency. He developed DECIEM to be a happy family (of people and beauty brands), rooted in kindness, creativity, diversity, and respect, alongside Co-Founder and CEO, Nicola Kilner.
We are growing rapidly and we’re looking for someone who shares this vision and wants to grow with us!

WHAT WE’RE LOOKING FOR

We are looking for a quality-oriented associate to help maintain quality during our manufacturing process.
This role will be based out of our manufacturing facility in Etobicoke.
Work hours for this position are between 11:30 PM to 7:30 AM

SKILLS AND QUALIFICATIONS NEEDED TO GET THE JOB DONE

• Strong computer skills in Microsoft office applications (Word, Excel)
• Team player with strong interpersonal skills.
• Ability to perform duties with a high level of accuracy and with minimal supervision
• Experience in cGMP regulated industry, quality control or similar role is required
• Relevant education in Science, chemistry, biochemistry, biology or another relevant field OR equivalent work experience is an asset

• Ensures all packaging lines are cleared for safety prior to start up
• Responsible for performing bulk testing at the filling stage (visual and PH testing), additional bulk mixing as per DECIEM Standard Operating Procedures (SOPs)
• Verify and approve primary and secondary packaging components prior to filling/unit boxing • Performs regular inspections on the packaged product for correct lot code
• Performs in-process checks as per approved DECIEM SOPs
• Continuously assesses results of inspection findings and react in a timely manner to communicate potential issues to Production Lead QA and Management
• Implement hold procedures for suspect product and/or product evaluations and testing
• Assist in writing Standard Operating Procedure (SOP) for newly established process and methods
• Document all packaging activities in MBPR in a timely and accurate manner according
• Initiate and/or make suggestions to improve the quality of work processes and products
• Apply the knowledge, skills and experience obtained to increase efficiency in solving new problems