Quality Assurance – Production QA Associate
The Packaging QC Associate will support the Supervisor in areas of safety, quality, GMP, productivity etc., however this position does not assume or replace the role of area supervisor. Ensure the quality of finished products by in-process line inspection and testing according to customer requirements and product specifications.
Etobicoke
What are we looking for?
The Packaging QC Associate will support the Supervisor in areas of safety, quality, GMP, productivity etc., however this position does not assume or replace the role of area supervisor. Ensure the quality of finished products by in-process line inspection and testing according to customer requirements and product specifications.
What would you be doing?
- Ensures all packaging lines are cleared for safety prior to start-up.
- Performs line clearance and line set up before line start-up.
- Perform additional bulk testing at the filling stage (Visual & pH testing), additional bulk mixing (Foundations) as per Deciem standard operating procedures.
- Verify and approve primary and secondary packaging components prior to filling/unit boxing.
- Performs regular inspections on the packaged product for correct lot code, primary and secondary packaging components.
- Performs In-process checks as per approved Deciem Standard operating Procedures.
- Continuously assesses the results of inspection findings and react in a timely manner to communicate potential problems to Production Lead QA and Quality Management.
- Implement Hold procedures for suspect product and or product evaluations and testing.
- Document all packaging activities in MBPR in timely manner.
- Reviews line MBPRs for completeness before being handed in for QA review and filing.
- Provides quality direction for line workers.
- Assist with investigations, consumer/customer complaints.
- Assist and provides support during third part audits.
- Initiate and / or make suggestions to improve the quality of work processes and / or product.
- Attends prescribed safety training programs required by the company.
- Perform other related duties as assigned.
What skills and qualifications do you need?
- Post-secondary diploma or degree related Science
- 2 years’ experience in cGMP regulated industry
- Experience with leadership and dealing with people
- Attention to detail
- Organized and good time management
- Proactive in learning
- Good documentation practices
- Adaptive and flexible
- Work with minimal supervision
- Able to multi-task and troubleshoot
Still interested?
Kindly send us your resume to vt@deciem.com. We really appreciate your effort in applying to this position. However, only those candidates who have been shortlisted for interviews will be contacted.
By emailing us your resume you agree to accept the Job Applicant policy that can be found here.
And the serious stuff:
DECIEM is an equal opportunity employer. We prohibit discrimination based on age, color, disability, national origin, race, religion, sex, sexual orientation, and any other legally protected class in accordance with applicable federal, provincial and local laws. We are also committed to creating and maintaining an inclusive and accessible workplace. If you are contacted for an interview and require accommodation during the interviewing process, please let us know.