QC Reviewer

Posted 8 Days Ago
Be an Early Applicant
Columbia, MO, USA
In-Office
Junior
Information Technology • Analytics • Biotech
The Role
Performs daily in-process quality control across laboratory projects, reviewing analyst documentation, reports, forms, and data tables for accuracy and compliance. Ensures adherence to SOPs, GLP, GCP, regulatory requirements, and company policies. Supports analysts with documentation, harmonizes laboratory procedures, responds to quality reports, and may develop and execute process-verification activities.
Summary Generated by Built In

About The Role

The QC Reviewer is responsible for performing quality control including daily in-process quality control on various projects. Ensures that all project's related documentation is filled out accurately and in a timely manner by the analysts and that all procedures are respected as per the company's SOPs.

What You'll Do Here

  • Perform daily in-process quality control on multiple projects inter-team.

  • Verify forms/paperwork, reports, and data tables generated by the analysts and scientist.

  • In charge of the quality within the laboratory according to GLP, regulatory agencies requirements and internal sops.

  • Support and mentor analysts during the generation of supplementary information forms as needed to ensure documentation accuracy and completeness.

  • Ensure harmonization of techniques, procedures, and documentation between analysts in the laboratory.

  • Conduct all work in compliance with the applicable SOPs, GCPs, GLPs, and observe all company guidelines and policies.

  • May respond to in-life QA report.

  • May perform process verification QC: develops processes, executes and reports.

What You'll Need to Succeed

  • College Degree and/or University degree in Biochemistry, Immunology or equivalent field.

  • Experience in the medical field/and or pharmaceutical fields with typically 2 years of experience in data review and quality control field. Must understand general SOPs and have knowledge of GLP regulations.

  • General advanced computer skills: proficiency working with MS-Office, Adobe Acrobat, Outlook.

  • Ability to multi-task and maintain organization in fast paced, changing environment. Strong planning and organizational skills.

  • Ability to work effectively and cooperatively in a team environment under significant time pressure. Demonstrated attention to detail and consistent ability to operate with accuracy and quality. Ability to successfully operate independently with minimal guidelines.

  • Ability to work holidays, weekends and evening hours as needed.

Work Authorization & Sponsorship

Applicants must be legally authorized to work in the United States. Altasciences is unable to provide sponsorship, sponsorship transfers, or visa maintenance for this position. All applicants must possess valid work authorization that does not require employer sponsorship now or in the future.

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

Altasciences' Incentive Programs Include: 

  • Training & Development Programs

  • Employee Referral Bonus Program

  • Annual Performance Review

#LI-ES1

Skills Required

  • College or university degree in Biochemistry, Immunology, or an equivalent field
  • Typically two years of experience in medical or pharmaceutical fields, data review, and quality control
  • Understanding of general SOPs and knowledge of GLP regulations
  • Proficiency with Microsoft Office, Adobe Acrobat, and Outlook
  • Ability to multitask and stay organized in a fast-paced, changing environment
  • Strong planning and organizational skills
  • Ability to work effectively and cooperatively in a team environment under significant time pressure
  • Strong attention to detail and consistent accuracy
  • Ability to work independently with minimal guidelines
  • Availability to work holidays, weekends, and evening hours as needed
  • Legally authorized to work in the United States without employer sponsorship
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The Company
HQ: Laval, Quebec
1,832 Employees
Year Founded: 1995

What We Do

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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