QC Reviewer, Sample Management (12-month contract)

220 Altasciences Company Inc; Laval; On-site; CAD 55,000 - 75,000; Full time

Benefits offered by this job

Training programs

Orientation bonus

Annual reviews

Job summary

Altasciences in Laval, QC seeks a Quality Control Reviewer for the Sample Management Department to ensure documentation quality and regulatory compliance. You will perform 100% QC on team output, conduct audits, and help develop SOPs for sample management and glass washing.

Strong attention to detail and bilingual communication are essential. Responsibilities include maintaining deviation records, responding to QA citations, updating training materials, and staying current with FDA-GLP, GCP, and

Qualifications

• High school diploma or higher in health sciences or equivalent with 3+ years of experience.
• Deep knowledge of FDA-GLP, GCP and TPD regulations.
• Experience in medical or pharmaceutical field is an asset.
• Bilingual in French and English; strong communication skills.

Responsibilities

• Perform 100% quality control on documentation from the sample management team.
• Conduct audits to ensure quality standards are met.
• Draft and revise standard operating procedures for sample management and glass washing.
• Maintain documentation tracking for deviations and non-conformances.
• Respond to QA citations and archive documentation.
• Keep up to date with regulatory developments (FDA, GLP, GCP, TPD).

Skills

GLP/GCP knowledge

Leadership

Problem-solving

Bilingual French/English

Communication

Education

Health sciences degree

Tools

Microsoft Access

Outlook

MS Office

Watson

Job description

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.

What you'll be doing here

• Perform 100% quality control on documentation generated by the sample management team.
• Responsible for quality within the sample management team.
• Perform audits within the team: develop, execute and write reports.
• 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.

What you need to succeed

• You have a high school diploma or higher in health sciences or equivalent with at least 3 years’ experience.
• You must have in-depth knowledge of FDA-GLP, GCP and TPD regulations.
• Experience in the medical or pharmaceutical field is an asset.
• Excellent management, organizational, communication (written and oral) and interpersonal skills.
• Strong GLP/GCP focus.
• Detail-oriented.
• Strong leadership, decision-making and problem-solving skills.
• Customer oriented.
• Must be bilingual (French and English).
• Software: Access, Outlook, MS-Office, Watson.

Altasciences strives to provide a French working environment for its employees in Quebec. Although as part of its francization program has taken all reasonable steps to avoid imposing the above-mentioned requirement. Fluency in English is an essential requirement for the position of QC Reviewer, Sample Management including, but not limited to, for the following reasons: The requirement to have study protocols, designs and clinical research documents written and documented in English as required by industry regulatory agencies.

At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well‑being of people across the globe.

Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences. We are better together and together We Are Altasciences.

What we offer

Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work. Altasciences' incentive programs include:

• Training and development programs
• Employee orientation bonus program
• Annual performance reviews
• #LI-MB1

Altasciences is an equal opportunity employer committed to diversity and inclusion. 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.

All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation.

Reasonable accommodations for persons with disabilities during the recruitment process are available upon request.

Join us at Altasciences!