More jobs:
QA Supervisor
Job in
Lansing, Ingham County, Michigan, 48900, USA
Listed on 2026-06-22
Listing for:
Scorpion Therapeutics
Full Time
position Listed on 2026-06-22
Job specializations:
-
Quality Assurance - QA/QC
Quality Engineering
Job Description & How to Apply Below
Description Overview
1st shift role;
Monday–Friday. Weekend coverage may be required on an on-call basis.
- 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.
- 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.
Competitive compensation; benefits for you and your family; career development opportunities;
Total Rewards information.
Click the APPLY button to submit an application; SAVE only saves profile.
Submit all application materials (resumes/CVs) in English.
#J-18808-LjbffrTo View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×