11 Quality Assurance And Engineering jobs in St. Louis.

Hiring now: Regulatory Affairs Jobs @ Parexel, Various Positions In Illi @ Baxter, Quality Control Coordinat @ Crescent, Validation Engr @ Biomérieux, Supv Production @ Mallinckro, Qc Scientist @ Steris, Cleanroom Certification S @ Vertex.Explore more at jobswithgpt.com.

🔥 Skills

manufacturing (3) cGMP (3) Regulatory Affairs (2) Consulting (2) Senior Regulatory Affairs Consultant (2) Labeling Operations (2) Home Based (2) Medical Device (2) healthcare (2) medical devices (2)

📍 Locations

East Saint Louis (5) St. Louis (3) Hazelwood (2) Edwardsville (1)

Parexel

Regulatory Affairs Jobs East Saint Louis
Skills & Focus: Regulatory Affairs, Consulting, Senior Regulatory Affairs Consultant, Vice President, Labeling Operations, Regulatory Lead, Home Based, Medical Device, Functional Service Provider, Canada-Remote

Baxter

Skills & Focus: healthcare, medical devices, parenteral nutrition, marketing, commercial, supply chain, engineering, quality assurance, research and development, manufacturing
About the Company: Baxter is a global medical device company that focuses on solutions for patients with chronic and acute conditions.
Type: Full time
Benefits: Comprehensive benefits options reflecting the value placed in employees.
Various Positions East Saint Louis
Skills & Focus: medical devices, quality, engineering, manufacturing, innovation, sales, healthcare, research and development, safety, collaboration
About the Company: Baxter is a global medical device and health care company focused on life-saving therapies. Our mission is to save and sustain lives.
Type: Full time
Benefits: Our comprehensive benefits options reflect the value we place in our employees.
Skills & Focus: Research and Development, Engineering, Medical Devices, Healthcare, Innovation, Clinical, Quality, Regulatory, Manufacturing, Product Development
About the Company: Baxter is a leading global medical products company that develops innovative solutions to save and sustain lives.
Type: Full-time
Benefits: Our comprehensive benefits options reflect the value we place in our employees.

Parexel

Regulatory Affairs Jobs East Saint Louis
Skills & Focus: Regulatory Affairs, Consulting, Medical Device, Clinical Regulatory, Labeling Operations, Drug & Device, Senior Regulatory Affairs Consultant, Home Based, FSP, Remote

Crescent

Skills & Focus: Quality Control, cGMP, Safety, Quality Assurance, Continuous Improvement, Productivity, Training and Mentorship, Regulatory Compliance, Lean Manufacturing, Problem Solving
About the Company: Crescent is committed to delivering top-quality products and maintaining a culture focused on safety, quality, and continuous improvement, while valuing its em…
Experience: Regulatory cGMP manufacturing experience
Benefits: $500.00 Sign on Bonus

Biomérieux

Skills & Focus: validation, protocols, ISO 13485, FDA, cGMP, documentation, statistical analysis, equipment, cleaning, process
Experience: 4 years of Validation experience in a related industry; or High School Diploma/GED with 8 years of Validation experience.
Skills & Focus: Project Management, scope, budget, planning, risk, quality, stakeholders, communication, microbiology, design controls
About the Company: bioMérieux is a global leader in in vitro diagnostics and is dedicated to improving patient health and ensuring consumer safety.
Experience: 5-7 years of experience in Project Management
Type: Full-time

Mallinckrodt

Skills & Focus: supervise, manufacturing, safety, training, lean manufacturing, team management, budget preparation, cGMP, OSHA, FDA
Experience: Minimum of three years manufacturing experience and two years supervisory experience.

Steris Corporation

QC Scientist St. Louis
Skills & Focus: quality control, ISO 9001, ISO 13485, MDSAP, FDA 21 CFR, test methodologies, validation methods, audits, chemical testing procedures, Failure Modes Effect Analysis
About the Company: STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention.
Experience: Minimum 6 years relevant lab testing in a regulated industry (i.e. FDA/ISO13485) required.
Type: Full-time

Vertex

Skills & Focus: cleanroom certification, ISO standards, FDA compliance, USP standards, particle counting, HEPA filter testing, environmental monitoring, regulatory compliance, technical documentation, contamination control