Altasciences

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.

This listing is sourced directly from Altasciences's careers page and normalized into a canonical job model.