QC Reviewer, Sample Management

Hiring By - Biostaffic



Job Highlights

Not Disclosed

Entry level

Posted 4 months ago
Job details
Your New Company!
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. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! 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.
About The Role
The QC Reviewer, Sample Management, is responsible for performing the quality control review of the documentation related to the Sample Management Team. The QC Auditor also performs audits within the team to ensure that quality standards are respected. He/she assists in the writing and/or reviewing of SOPs pertaining to sample management and glass washing.
What You'll Do Here
  • Performs 100% quality control review on documentation generated by the Sample Management team.
  • In charge of the quality within the Sample Management team.
  • Performs audits within the team: develops, executes and reports.
  • Fills out supplementary information forms as needed to ensure documentation is accurate and complete.
  • Completes documentation as required to track deviations and reports of non-compliance within the team.
  • To respond to QA citations.
  • Performs documentation archiving.
  • To write, revise and/or review SOPs pertaining to sample management and glass washing.
  • To write, review and/or update training documents.
  • To keep up to date with respect to pertinent regulatory developments in the industry.
  • To conduct all work in compliance with applicable SOPs, GCPs, GLPs, and observe all company guidelines and policies.
  • Stay up to date on new SOPs, procedures, and techniques via training sessions, team meetings and internal communication avenues.
What You'll Need To Succeed
  • Bachelor/or higher degree in sciences or relevant equivalent experience.
  • Must possess an in-depth knowledge of FDA-GLP, GCP and TPD regulations.
  • 3 to 5 years experience in QC.
  • Experience in the medical or pharmaceutical field is an asset.
  • Excellent management, organizational, communication (both written and verbal) and interpersonal skills.
  • Strongly GLP/GCP-minded.
  • Attentive to details.
  • Strong leadership, decision making and problem solving ability.
  • Customer-focused.
  • Must be bilingual ; French and English ; Written and writing.
  • Software Watson LIMS (Asset)
  • Software: Intermidiate level for Access, Outlook, MS-Office.
  • Must be flexible in terms of working hours (available to work between 8 a.m. and 7 p.m.)
  • Hybrid work between lab and office.
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' Benefits Package Includes
  • Health/Dental/Vision Insurance Plans
  • 401(k)/RRSP with Employer Match
  • Paid Vacation and Holidays
  • Paid Sick and Bereavement Leave
  • Employee Assistance & Telehealth Programs
  • Telework when applicable
Altasciences' Incentive Programs Include
  • Training & Development Programs
  • Employee Referral Bonus
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!
Apply Now

Benefits Offered?

  • No

Bonus Offered?

  • No

Travel Required?

  • No


  • Canada


  • Entry level

Global Experience Needed?

  • No

Specialized Experience Needed?

  • No

Apply before:

  • Apr 12, 2024
Company Overview

Current Openings: 0

Outsourcing made easy with a one-stop solution to early phase drug development. We are an integrated drug development solution company, offering pharmaceutical and biotechnology companies a proven, flexible approach that removes the need for multiple service providers during the early stages of drug development. Whether for one study or an end-to-end program, we help you reach critical decision-making milestones sooner by improving speed and ease from lead candidate selection to clinical proof of concept, and beyond. When partnering with Altasciences, you can experience up to 40% in time savings thanks to our integrated, one-stop solution offering. We strive to create a true partnership with our clients, our partners, and our colleagues that enables a mutually supporting relationship built on a combination of excellent science and solid communication. Helping sponsors get better drugs to the people who need them, faster, for over 25 years. Our full-service offering is always tailored to your specific research needs: - Preclinical research - Clinical pharmacology - Drug formulation - Manufacturing and analytical services - Bioanalysis - Program management - Medical writing - Biostatics - Data management - And so much more!
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