Senior Supplier Quality Engineer
Apply NowCompany: Kindeva Drug Delivery
Location: Saint Louis, MO 63129
Description:
Our Work Matters
At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.
The Impact You Will Make
The Senior Supplier Quality Engineer provides oversight, component/issue evaluation, and corrective action of all production and supplier quality related issues for external supplier processes and suppliers based on commodity class assigned.
Role Responsibilities
Basic Qualifications
Preferred Qualifications
#LI-On-Site
California residents should review our Notice for California Employees and Applicants before applying.
Equal Opportunity Employer:
Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.
Do you see yourself as part of the Kindeva mission? Click Apply Now Today!
Other details
Apply Now
At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.
The Impact You Will Make
The Senior Supplier Quality Engineer provides oversight, component/issue evaluation, and corrective action of all production and supplier quality related issues for external supplier processes and suppliers based on commodity class assigned.
Role Responsibilities
- Designs and executes Quality Engineering related protocols; summarizes studies to ensure consistency of data production and compliance with manufacturer and Kindeva specifications/requirements and with current Good Manufacturing Practices.
- Responsible for quality and process related issue management for suppliers/vendors.
- Responsible for applicable process documentation to provide production process control ensuring performance within validated parameters.
- Owner for assigned projects, responsible for project management and task execution.
- Knowledgeable with statistical analysis using control charts, process capability, hypothesis testing, Gage R&R, ANOVA, and design of experiments. Familiar with using MINITAB.
- Analyzes data and issues memos, reports, and presentations concerning Quality Engineering projects or areas of interest.
- Evaluates equipment or process problems and designs testing and investigation plans to determine possible causes or solutions; assists in determining process capability of new equipment. May also be called on to harmonize measurement techniques between the site and supplier.
- Ensures product development activities have all necessary Quality Engineering support.
- Interacts with third party customers, outside testinglaboratories and provides Quality Engineering assistance where needed on specific issues.
- Assists in identifying root causes and coordinates corrective action to quality issues.
- Ensures product or component traceability and quarantine as necessary.
- Assist QCD lab supervisor with technical issues involving product functionality, component testing, and protocol execution.
- Assists in compiling quality data including gage R&R studies, process capability studies, first article inspections, trending of product defects, trending of functionality data for finished product, dimensions on components or finished product, raw material inspection/sampling, incoming component inspection.
- Owner of Quality System Records, including but not limited to: SCAR, Change Management, Commitment Tracking, MIR/QAR/ER, MDCP CAPA, Action Items, Interim Report.
Basic Qualifications
- BS in an Engineering related field, with a minimum of 5 years of medical device or pharmaceutical Quality Engineering related experience.
- Process and Material Skills: Familiarity with some of the following manufacturing processes - medical device glass cartridge or vial, plastic injection molding, rubber compounding and molding, printed labels and packaging. Familiar with various measurement gages used in Quality labs, knowledge of various types of mechanical testing.
- Thorough knowledge of cGMPs. Good working knowledge of associated industry and regulatory guidance documents, FDA guidelines, ISO standards, ASTM standards, etc. Excellent knowledge/understanding of protocol acceptance criteria and capable of determining appropriate Corrective Action/Preventive Action (CAPA) for recommendation to management.
- Must have the ability to travel 10% to visit suppliers in US and International locations as needed.
Preferred Qualifications
- Certified Quality Engineer, Six Sigma training or Lean Manufacturing training.
#LI-On-Site
California residents should review our Notice for California Employees and Applicants before applying.
Equal Opportunity Employer:
Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.
Do you see yourself as part of the Kindeva mission? Click Apply Now Today!
Other details
- Job Family D - Quality - Supplier Quality
- Job Function D - Quality
- Pay Type Salary
Apply Now