Altasciences
QC Reviewer, Sample Management (18 Months contract)
Laval, Quebec
Sponsorship not specifiedDetected 19 days ago
GCPPerformance ManagementFDA RegulatoryLeadershipCommunicationProblem SolvingMicrosoft Office
About the role
- The Quality Control Reviewer, Sample Management Department, is responsible for the quality control review of documentation related to the Sample Management team.
- He/she also conducts audits within the team to ensure that quality standards are met.
- He/she participates in the drafting and/or revision of standard operating procedures for sample management and glass washing.
Responsibilities
- Perform audits within the team: develop, execute and write reports.
Requirements
- You must have in-depth knowledge of FDA-GLP, GCP and TPD regulations.
- Must be bilingual (French and English).
Skills
- Excellent management, organizational, communication (written and oral) and interpersonal skills.
- Strong leadership, decision-making and problem-solving skills.
Compensation
- Annual performance reviews
Benefits
- Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.
- Altasciences' benefits package includes:
- Health/Dental/Vision Insurance Plans
- Paid Vacation and Holidays
- Paid Sick and Bereavement Leave
- Employee orientation bonus program
- Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives.
Company info
- Completes additional information forms as necessary to ensure documentation is accurate and complete.
- Complete documentation necessary to track deviations and non-conformance reports within the team.
- Respond to QA citations.
- Archive documentation.
- Write, revise and/or review standard operating procedures for sample management and glass washing.
- Write, revise and/or update training materials.
- Keep abreast of relevant regulatory developments in the industry.
- Perform all work in accordance with applicable SOPs, GCPs and GLPs and adhere to all company guidelines and policies.
- Keep abreast of new SOPs, procedures and techniques through training sessions, meetings and internal communications.
- You have a high school diploma or higher in health sciences or equivalent with at least 3 years' experience.
- Experience in the medical or pharmaceutical field is an asset.
- Strong GLP/GCP focus.
Equal opportunity
- equal opportunity employer committed to diversity and inclusion.
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This listing is sourced directly from Altasciences's careers page and normalized into a canonical job model.