Astrix · 1 day ago
QMS Supervisor - Biologics
Astrix is a dynamic biopharmaceutical company seeking an experienced Quality Systems/QMS Supervisor to lead quality management initiatives within a biologics manufacturing environment. The role involves overseeing QMS activities, ensuring compliance with global regulatory standards, and driving continuous improvement initiatives.
Responsibilities
Oversee all QMS activities including investigations, CAPA, documentation control, and report writing
Lead and manage PPQ and cleaning validation projects to support product and process integrity
Ensure ongoing compliance with FDA, EMA, ICH, and other global regulatory standards
Provide leadership and mentorship to quality team members; foster collaboration across manufacturing, validation, and regulatory teams
Support audits, inspections, and regulatory reviews, ensuring readiness and robust documentation
Drive continuous improvement initiatives, strengthening the QMS and aligning with industry best practices
Qualification
Required
Bachelor's degree in Life Sciences or a related field
6+ years of biologics manufacturing experience, with at least 3 years focused on QMS leadership
In-depth knowledge of upstream and downstream biologics processes
Demonstrated experience in investigation report writing, CAPA, and documentation management
Strong background in PPQ, cleaning validation, and global GMP/regulatory compliance
Company
Astrix
Astrix is the unrivaled market-leader in creating & delivering innovative strategies, solutions, and people to the life science community.
H1B Sponsorship
Astrix has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (10)
2024 (9)
2023 (10)
2022 (16)
2021 (11)
Funding
Current Stage
Late StageRecent News
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