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Piramal Pharma SolutionsVerified Job Source

QUALITY CONTROL CHEMIST

  • Aurora, ON
  • On-site
  • Posted Sep 1, 2026
  • 1 position

$25–$28 / hour

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Employment type
Full-time
Experience level
Entry, Junior · 0+ years
Posting language
English
Working hours
40 hours per week

Job summary

Perform laboratory testing and shift activities to support manufacturing and analytical services in compliance with quality standards. Conduct lab investigations, maintain documentation, and ensure adherence to cGMP and GLP protocols.

Job details

Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide. For more details, please visit : www.piramalpharmasolutions.com Job Title QUALITY CONTROL CHEMIST I Job Description Perform lab testing to standards of quality and efficiency in support of our customers and our production facilities. Execute shift activities related to manufacturing as prioritised by the QC Manager or senior member Competent in lab instrumentation, procedures and activities (ie. raw material method development, IPC product, raw material testing and as required all testing/calibration activities in support of Analytical Services activities) Conduct required testing and lab activities (including third party and stability activities as requested) under current Good Manufacturing practices (cGMP) in support of new projects and manufacturing and including data interpretation, documentation and reporting of results, calibrations and PMs under the direction of senior staff Initiate lab investigations and deviations as per internal SOPs under the direction of QC Manager or designate (eg. out-of-specification reports) Work as an effective team member to meet departmental goals, sharing knowledge with team members Communicate troubleshooting issues to on-shift senior staff (e.g. procedural, instrument or method issues). Maintain active continuous cross-training in support of other departmental objectives (eg. lab initiatives) Ensure compliance to cGMP and Good Laboratory Practices (GLP) according to in-house SOPs. Introduction to reviewing analytical documentation for analysis performed by other chemists under the direction of senior staff Participate in opportunities to develop and disseminate current knowledge of analytical chemistry and technology Promote and ensure safe and clean lab operations Perform departmental tasks such as cleaning supply ordering, instrumentation/technology training, etc (as required) Perform other duties as assigned Canada Salary Range :CAD24.50 - CAD28.00/Per Hour

What you’ll do

Perform laboratory testing and shift activities to support manufacturing and analytical services in compliance with quality standards. Conduct lab investigations, maintain documentation, and ensure adherence to cGMP and GLP protocols.

Requirements

The role requires competency in laboratory instrumentation, analytical procedures, and the ability to work effectively within a team environment. Candidates must be able to interpret data, troubleshoot technical issues, and maintain rigorous documentation standards.

Listed skills

  • Quality Control · Preferred
  • Documentation · Preferred
  • Reporting · Preferred
  • Troubleshooting · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

  • Laboratory testing
  • Analytical chemistry
  • cGMP
  • GLP
  • Instrumentation
  • Method development
  • Data interpretation
  • Documentation
  • Troubleshooting
  • Quality control
  • Calibration
  • SOP compliance
  • Laboratory safety
  • Reporting
  • Current Good Manufacturing Practices (cGMPS)
  • Good Laboratory Practice (GLP)
  • Data Interpretation
  • Method Development
  • Application Programming Interface (API)
  • Analytical Chemistry
  • Good Manufacturing Practices
  • Clinical Trials
  • Drug Discovery
  • Laboratory Testing
  • Operations
  • Pharmaceuticals
  • Troubleshooting (Problem Solving)
  • Investigation
  • Quality Control

Job areas

  • Science & Research
  • Manufacturing
  • Healthcare
  • Quality Control Chemist
  • Chemists

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