JP Laboratories is looking for qualified and experienced employees to join our successful team. We currently have the following full-time position in our Mississauga location:

Quality Assurance Associate – 1 position

Responsibilities:

- Manage the GMP Documentation, SOP, Change Control, CAPA, OOT, OOS, Training Record systems.
- Review and approve CoA and other quality documentation
- Oversee Quality Control documentation to enforce good documentation practice to improve accuracy, GMP compliance and neatness of analytical documentation
- Verify calculations and documented information such as reagent expiry, instrument calibration, logbook entries, control charts etc are present and complete and accurate.
- Review internal logbooks for incoming samples, standards, reagents, equipment etc.
- Issue and reconcile Quality Control laboratory workbooks and other GMP documentation.
- Audit and inspect laboratory equipment daily use logbooks
- Ensure analysis performed are as per client’s specification
- Prepare, review and approve Standard Operating Procedures (SOPs)
- Archive and retrieve quality control data
- Participate in client audits, regulatory audits and inspections
- Perform Annual Internal Audit, and work with Analytical Lab personal to ensure follows up and corrective actions are completed.
- Periodic review of training records, SOPs, Change Control implementation, Deviation and OOS investigation
- Data-review and data-verification activities
- Conduct QA investigation with regard to Out-of-Specifications, Exceptions and Corrective Action. Monitor effectiveness of corrective and preventative actions.
- Assist in the review and approval of GMP documents such as SOPs, and associated forms, and initiate revisions.




- Any other tasks assigned by the JPL senior management

Education and Experience:

- University Degree in Science – preferably in Chemistry
- Minimum 3 years of experience in the review of raw data and Quality management systems.
- Have expert experience of GMP Thorough understanding of pharmaceutical QA Systems, US, EU, and Canadian GMP regulations
- Knowledge of GMP, GLP, Compendia, analytical techniques
- Excellent verbal and written communication skills, interpersonal skills and you should be extremely results driven and organized

General Skills:

- The requirements listed below are representative of the knowledge, skill, and/or ability required.
- Must be willing to work in a team-based environment
- Must have solid math skills
- Must be able to work with limited direct supervision
- Must have valuable problem solving/organizational skills
- Must have excellent computer skills
- Must have strong writing and communication skills in English
- Must have the ability to analyze data
- Must be attentive to detail
- Must have excellent organizational skills to meet frequent changes in immediate priorities, problem solving skills, and understanding of various computer software programs required

The above positions are only applicable to permanent residence and/or Canadian citizens with a minimum degree in science. To apply, please reference “QA Associate” in subject line and submit resume and cover letter with salary expectation to [email protected]

We thank all applicants for their interest, however, only those selected for an interview will be contacted. No phone calls please.

Pay: $38,000.00-$55,000.00 per year

Benefits

- In office parking

Work Location: In person

📌 Quality Assurance Associate (Mississauga)
🏢 JP Laboratories
📍 Mississauga