Quality Assurance Manager
Greater St. Louis, MO, US
Scientific
Bachelors Degree
Full Time, Direct Hire
$120K-$130K
Manager (Manager/Supervisor)
On-site
Biotechnology/Pharmaceuticals
First Shift (Day)
Greater St. Louis, MO, US
$120K-$130K
Manager (Manager/Supervisor)
Full Time, Direct Hire
Biotechnology/Pharmaceuticals
On-site
Scientific
Bachelors Degree
First Shift (Day)
Job details
Quality Manager – (Greater St. Louis, MO Area)
Sign-On Bonus
Day Shift
The Quality Manager is a critical member of the Site Leadership Team in the Greater St. Louis, MO facility. Reporting to the business unit Quality Director, this role is the champion for quality culture and continuous improvement.
You will be responsible for creating a climate of trust, driving cross-functional collaboration, and building a robust, state-of-the-art Quality Management System (QMS) that ensures safety, compliance, and customer satisfaction across all operational areas.
Job Responsibilities:
I. Leadership & Culture Development
- Develop a strong quality culture by leading, training, coaching, and motivating quality inspectors, lab technicians, and the document controller.
- Partner with site leadership across safety, productivity, customer-service, and security initiatives to resolve operational challenges and identify work process improvements.
- Lead all GMP-related activities on site, ensuring robust training and adherence to standards.
- Provide leadership, coaching, and counseling to develop team members’ interpersonal and technical skills.
II. Technical & Laboratory Management
- Manage a multi-shift crew including quality inspectors, lab technicians, and a document controller.
- Oversee the QC Laboratory, which is responsible for the analysis of raw materials and compounded materials.
- Manage quality inspection actions and resolve product quality standard applications by accurately interpreting specifications.
- Utilize advanced analytical methods including Gas and Liquid Chromatography, Elemental Analysis, Titration, Infrared Spectrometry, and more to manage investigations and process validations.
III. Quality Systems & Compliance
- Lead site investigations of non-conformances using effective root cause analysis (RCA) and implement robust corrective and preventive actions (CAPA).
- Drive team efforts for collecting, analyzing, and summarizing product quality results data and trends to inform continuous improvement initiatives.
- Lead and support external customer and regulatory audits, as well as internal audits.
- Develop and maintain all quality systems at the facility, ensuring they meet current Good Manufacturing Practice (GMP) standards.
- Provide quality management support for both new product introduction and current product sustaining activities.
Required Qualifications:
- Bachelor’s degree in a relevant field (Chemistry, Engineering, Biology, or related science preferred).
- Minimum of 5 years of quality management or supervisory experience in a metrics-driven GMP manufacturing environment (Food, Pharma, Cosmetic, OTC, Personal Care).
- SAP knowledge is a must.
- Proven experience in setting up and maintaining robust quality systems and a thorough knowledge of GMP standards.
- Excellent writing, communication, and Microsoft Office skills.
Benefits & Rewards
Company offers a robust suite of benefits designed to support your total well-being, growth, and security:
- Financial Security:
- 401(k) with a generous company match.
- Bonus incentive programs (based on individual and organizational performance).
Join the team and help us deliver excellence, safely and efficiently, every day.
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