GLP QC Reviewer — Lab Quality & Documentation

Altasciences; Columbia Township (MO); On-site; USD 48,000 - 64,000; Full time

Benefits offered by this job

Health/Dental/Vision Insurance

401(k) with employer match

Paid vacation and holidays

Paid sick and bereavement leave

Employee assistance & telehealth

Training & development programs

Employee referral bonus

Annual performance review

Job summary

Altasciences is seeking a QC Reviewer to perform daily in-process quality control across projects and ensure all documentation aligns with SOPs and GLP standards. You will verify forms, data tables, and reports produced by analysts and scientists while mentoring staff to maintain accuracy.

Ideal candidates hold a relevant degree and 2 years in medical/pharmaceutical data review, with strong computer skills and flexibility to work varied hours as needed.

Qualifications

• College degree in Biochemistry, Immunology or equivalent field.
• 2 years in medical/pharmaceutical data review or QC with GLP knowledge.
• Proficient in MS-Office, Adobe Acrobat and Outlook.
• Ability to multi-task in a fast-paced environment with accuracy.
• Willingness to work holidays, weekends and evenings when needed.

Responsibilities

• Perform daily in-process quality control on multiple projects inter-team.
• Verify forms, reports, and data tables generated by analysts and scientists.
• In charge of lab quality per GLP and internal SOPs.
• Mentor analysts to ensure documentation accuracy.
• Ensure harmonization of techniques and documentation between analysts.
• Work in compliance with SOPs, GCPs, GLPs and company policies.
• Respond to in-life QA reports as needed.
• Develop, execute, and report process verification QC.

Skills

Attention to detail

Multi-tasking

Team collaboration

Strong planning

Organizational skills

Education

Bachelor’s degree in Biochemistry/Immunology or equivalent

Tools

MS-Office

Adobe Acrobat

Outlook

Job description

Altasciences is seeking a QC Reviewer to perform daily in-process quality control across projects and ensure all documentation aligns with SOPs and GLP standards. You will verify forms, data tables, and reports produced by analysts and scientists while mentoring staff to maintain accuracy.

Ideal candidates hold a relevant degree and 2 years in medical/pharmaceutical data review, with strong computer skills and flexibility to work varied hours as needed.