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QA Supervisor

Job in Lansing, Ingham County, Michigan, 48900, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-06-22
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Description Overview

1st shift role;
Monday–Friday. Weekend coverage may be required on an on-call basis.

Scope of the Role
  • Develop and maintain auditing/testing methods to ensure identity and control of packaging materials, including approval of components for production.
  • Review/approve controlled documents: SOPs, SWIs (Standard Work Instructions), Job Aids, SCRF (SAP Change Request Form), Rework (RW) notifications, planned deviations, and supplier advisories.
  • Coordinate initial response activities including risk assessments.
  • Lead/own investigations for packaging incoming out-of-specification and deviation events; identify nonconformances/variances and recommend corrective actions; ensure follow-up with staff/management.
  • Manage and train non-exempt staff to ensure documentation meets cGMP and FDA standards.
  • Assist with FDA inspections and maintain FDA readiness in Operations; assist with third-party audits (Customer/Contract).
  • Select, mentor, and evaluate staff; provide quality coaching and guidance to floor-level operations.
  • Manage day‑to‑day workload, shifting priorities, and initiate/execute/oversee projects as required.
Experience Required
  • Bachelor’s degree in a scientific discipline strongly preferred; alternatively, non-degreed with substantial QA or regulated manufacturing/packaging knowledge.
  • 4+ years in a Quality role, preferably with leadership responsibilities.
  • Exceptional people management; prior people leader experience strongly preferred.
  • Strong oral/written communication and interpersonal skills.
  • Previous FDA-regulated industry experience preferred; knowledge of product quality and/or manufacturing/packaging processes.
  • Leadership/supervisory experience highly preferred.
  • Ability to interpret/apply regulations to product quality and processes.
  • Familiarity with cGMP, QA, release methods, auditing and/or risk assessment in an FDA-regulated environment highly preferred.
  • SAP knowledge preferred.
Benefits

Competitive compensation; benefits for you and your family; career development opportunities;
Total Rewards information.

Application Instructions

Click the APPLY button to submit an application; SAVE only saves profile.

Submit all application materials (resumes/CVs) in English.

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