Data Quality Specialist
2 months ago
Groupe Parima is searching for a dedicated Data Reviewer to ensure the accuracy and integrity of analytical data within our pharmaceutical operations.
As a key member of our quality assurance team, you will play a vital role in upholding the highest standards of Good Manufacturing Practices (GMP) throughout all stages of product development and manufacturing.
Your Responsibilities:
- Meticulously review documentation related to chemistry, microbiology, raw materials, and packaging materials analyses, ensuring strict adherence to established protocols and specifications.
- Conduct thorough reviews of validation, verification, or transfer documentation for analytical methods, guaranteeing compliance with industry standards.
- Critically analyze analytical results, identifying any discrepancies and implementing corrective actions to maintain data integrity.
- Approve and disseminate stability summaries to clients, providing comprehensive reports on product performance over time.
- Actively participate in laboratory investigations, contributing your expertise to resolve any deviations or issues that arise.
- Develop and refine laboratory-related procedures, ensuring clarity and consistency across all operations.
Your Qualifications:
- Possess a College Diploma in Science (Chemistry, Biochemistry), or a related field.
- Demonstrate proven experience in Quality Control within the pharmaceutical industry.
- Exhibit a comprehensive understanding of Canadian Good Manufacturing Practices (GMP) as defined by Health Canada.
- Be familiar with pharmacopeias (USP, Ph. Eur., and BP) and their practical applications in a laboratory setting.
- Showcase exceptional attention to detail and a commitment to accuracy in all tasks.
- Thrive in a collaborative environment and possess strong communication skills.
- Be fluent in both French and English.
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