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Pyramid Labs

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6 jobs
Pyramid Labs
15 hours ago

Manufacturing Supervisor

NewBe an early applicant North America
United States

POSITION SUMMARY: Under general direction, the Manufacturing Supervisor is responsible for the day-to-day leadership, supervision, and execution of GMP-compliant fill/finish manufacturing operations. This position…

ERP NetSuite
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Pyramid Labs
1 views 5 days ago

Sr. Validation Engineer

New North AmericaSenior
United States

Position Summary The Senior Validation Engineer is responsible for leading and executing validation activities supporting sterile injectable and biopharmaceutical manufacturing operations. This role ensures that…

Airflow Automation FMEA Risk Assessment SCADA +1 skills
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Pyramid Labs
1 views 5 days ago

Manufacturing Technician (Temp)

New North America
United States

POSITION SUMMARY: The Temp Manufacturing Technician performs various manufacturing related activities for a GMP compliant Fill/Finish operation, applying standard practices, techniques, and procedures. The Technician…
Pyramid Labs
3 views 5 days ago

Microbiology Supervisor

New North America
United States

POSITION SUMMARY: Reporting to the Director of Microbiology, the QC Microbiology Supervisor is responsible for overseeing the daily operations of the Quality Control Microbiology laboratory, ensuring compliance with…

Root Cause Analysis
Pyramid Labs
3 views 5 days ago

Project Manager

New North AmericaContract
United States

Project Manager at Pyramid Labs (Pyramid Pharma Services), a pharmaceutical contract manufacturing organization in Costa Mesa, CA. Day to day: managing a portfolio of client programs — tracking timelines, risks, and project financials — while owning client accounts, running meetings, and identifying new business opportunities. Requires 6+ years of PM experience in biotech/pharma/CMO settings.

Business Development PMP
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Pyramid Labs
2 views 5 days ago

Sr. QA Specialist

New North AmericaSenior
United States

Senior QA Specialist at a pharmaceutical CDMO who leads review of complex batch production records for FDA/EMA/GMP compliance prior to product release, drives deviations/CAPA and change control, mentors junior QA staff, and serves as SME during regulatory and client audits. Day-to-day tools include eQMS platforms and Microsoft Office.

Regulatory Compliance Six Sigma
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