Quality Inspector - Mississauga, Canada - Contract Pharmaceuticals

Contract Pharmaceuticals
Contract Pharmaceuticals
Verified Company
Mississauga, Canada

1 month ago

Sophia Lee

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Sophia Lee

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Description

Quality Inspector - Midnight Shift
Contract Pharmaceuticals Limited is a contract manufacturer and packager of prescription and over the counter pharmaceutical products.

We are dedicated to providing comprehensive and innovative outsourcing services that exceed the uncompromising demands of the global pharmaceutical industry.

To provide quality oversight to support daily Manufacturing, Packaging and Warehouse Operations.


SPECIFIC RESPONSIBILITIES:


Perform line checks during packaging processes

  • Verify correctness of documents and components present in the packaging suite.
  • Perform random inprocess checks (i.e. product appearance, fill weight, presence of lot number and expiry date, etc.)
  • Spot check documents/logbooks to ensure accurate documentation of the packaging process.
  • Observe activity within the packaging area to ensure compliance with GMP
  • Interact with Supervisors to answer GMP questions.

Perform manufacturing walk-through during production

  • Verify correctness of documents and components present in the manufacturing suite.
  • Spot check documents/logbooks to ensure accurate documentation of the manufacturing process.
  • Observe activity within the manufacturing area to ensure compliance with GMP
  • Interact with Supervisors to answer GMP questions.

Perform warehouse walk-through

  • Observe activity within the warehouse area to ensure compliance with GMP
  • Interact with Supervisors to answer GMP questions.
  • Provide guidance to enhance GMP understanding and promote Good Documentation Practices (GDP).
  • Make quality decisions regarding Manufacturing, Packaging, and Warehouse issues as required according to SOP's. Escalate significant issues to Quality Management.
  • Provide assistance in troubleshooting issues encountered during production.
  • Participate as a member of the Investigation Team to assess potential impact to product quality.
  • Approve Master Coding Requirements for Lot Number and Expiry Date, and Master Shipping Case Labels according to customer requirements.
  • Perform CAPA effectiveness checks as required.
  • Other duties as assigned.

QUALIFICATIONS:

  • Bachelor of Science or college diploma preferably in a scientific discipline, with a minimum of 3 years of Pharmaceutical Manufacturing or QA experience.
  • Knowledge of Health Canada and US FDA GMP requirements for Pharmaceutical Manufacturing.
  • Knowledge of computer systems such as SAP and Microsoft Office Excel.
  • High attention to detail in reviewing documents for accuracy and compliance to specifications.
  • Good verbal and written English communication skills.
  • Flexible with the ability to adapt, respond quickly and manage change in a fastpaced environment.
  • Demonstrated competencies in CPL's core values Fairness, Trust, Respect, and Integrity.
WORKING CONDITIONS*- Production environment.

We thank all applicants for their expression of interest; however only those selected for an interview will be contacted. No phone calls or agencies please.
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