CareerPlan

Study Lead - BioPharmaceuticals (GMP Lab)

Middleton, Wisconsin, USAFull-time2026-10-26 → 2026-11-10
On-siteNo visa sponsorship

Core

Managing multiple routine bioanalytical projects (release, stability, quality control) in a GMP laboratory setting, ensuring data integrity and regulatory compliance.

Role type

Senior IC study lead (bioanalytical testing)

Builds

Routine study outputs, scientific reports, and quality records for clients

Domain

Life Sciences / BioPharmaceuticals / GMP Laboratory

Required skills

GMP compliance, routine analytical testing, data integrity, project management, technical writing, data analysis, SOP adherence, risk assessment, mentoring

Preferred skills

Familiarity with data collection software, Microsoft suite proficiency, problem-solving

Technologies

Analytical instruments, detection techniques, Microsoft Office suite, data collection software

Responsibilities

Manage routine study timelines and deliverables; review and evaluate data; write protocols and reports; communicate with clients and stakeholders; mentor laboratory staff; ensure audit readiness; escalate non-routine issues.

Seniority

Senior, hands-on IC