Q.A. / Q.C. ASSOCIATE

Jaapharm Canada Inc.

Woodbridge (Vaughan), ON, Canada

Jaapharm located near Hwy. 7 & Weston Road specializes in solid dosage pharmaceutical products, in-house research, manufacturing, packaging and testing. 80% of total budget in R&D, relates to analytical chemistry method development and compression process development, at present.

Founded in 1988, Jaapharm’s focus is directed towards the research in compression (tablet) & analytical method validation for raw material & finish products relating to compression.

Q.A. / Q.C. ASSOCIATE

Assists in providing oversight and on-going development of QA System updates, QA In-Process, QA reference to Sanitation Control procedures, the Quality Assurance relating to manufacturing & Packaging.

Responsibilities:

• Checking and completing Packaging product room Start up & Closing documents.
• Updating all daily, weekly & monthly Maintenance Report.
• Assure compliance to all Regulatory and Corporate guidelines and requirements.
• Typical Quality Control functions such as reviewing and auditing batch documents, laboratory test results relating to Finished Product, Stability and Raw Materials.
• Approves raw materials, packaging and labeling materials.
• Investigates and records complaints.
• Reviews Analytical Data.
• Ensures correct reconciliation (product, label)
• Investigates processes (Out-of-Specification test results and deviations)

Requirements:

• University Degree in Science and approved course in Quality Assurance an asset.
• Minimum of 1 year Quality Assurance experience in the pharmaceutical industry in particular, OTC Drugs.
• Participation in Health Canada Inspection a definite asset.
• Knowledge of GMP, U. S. Pharmacopeia.
• Superior organizational and interpersonal skills.
• Supporting documentation related to education, training and work experience will be required.
• Has the appropriate training, experience and technical knowledge in reference to GMP.
• Ability to manage multiple projects and tasks concurrently and effectively.
• Sound understanding of cGMP and ICH requirements.
• Excellent written and oral communication skills is a must.
• Computer proficiency with MS Office programs.

Job Types: Full-time, Permanent

Salary: $52,000.00-$64,000.00 per year

Schedule:

• 8 hour shift

COVID-19 considerations:
Everyone is required to wear face mask in the premises. Hand sanitizing protocol followed at the facility. Social distance to be maintained at all times in the premises. Should be fully vaccinated.

Education:

• Bachelor's Degree (preferred)

Experience:

• Quality Assurance experience in pharmaceutical industry: 1 year (preferred)

Language:

• English (preferred)

Work Location: In person

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