Top 10 Senior validation engineer Jobs in Memphis Tn

Sr Quality Engineer
bioventus —Memphis, TN
- Full-time
- Senior level
- Electrical Engineering
- 4 years
Senior Process Engineer - MSAT
Rose BioSolutions —Memphis, TN
- $110,000 - $123,200 a year
- Full-time
- Ability to walk for extended periods
- Bachelor of Science
- Engineering
- Health insurance
- Dental insurance
Quick Apply
Senior Data Engineer
Intellivo —Memphis, TN
- Full-time
- Computer Science
- Bachelor of Science
- HIPAA
Quick Apply
Senior Mechanical Design Engineer
Barnhart Crane & Rigging —Memphis, TN
- Full-time
- Background check
- 7 years
- Microsoft Excel
- Disability insurance
- Health insurance
Quick Apply
Manufacturing Engineer I, II or Sr.
MicroPort Orthopedics Inc. —Arlington, TN
- Management
- Engineering
- Mid-level
- Paid holidays
- Disability insurance
Quick Apply
Senior Image Data Scientist-Center for Bioimage Informatics
St. Jude Children's Research Hospital —Memphis, TN
- $86,320 - $154,960 a year
- Full-time
- Computer Science
- Java
- Master's degree
Senior Software Engineer
TaxPlanIQ —United States
- $100,000 - $140,000 a year
- Email
- Remote
- Background check
- System design
- Java
- Health insurance
- Dental insurance
Quick Apply

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Sr Quality Engineer

bioventus -
Memphis, TN

Apply Now

Job Details

Full-time

Qualifications

GD&T
Medical device manufacturing facility experience
Engineering product development
Biomedical regulatory compliance
ISO 13485
FDA regulations

Full Job Description

Are you ready to work for a more active world?

At Bioventus, our business depends on developing our people. We invest in you and challenge you to be the best. We value our colleagues for their different perspectives and individual contributions, and our leaders listen. Our success rests on working together to achieve shared goals and rewards. Join a diverse team of global colleagues driven to help patients resume and enjoy active lives.

The Sr Quality Engineer provides quality engineering expertise to manufacturing, engineering, quality control/assurance and process/product development teams to ensure our products are designed and manufactured to a high level of quality, and compliant with medical device regulations.

What you'll be doing

Ensure medical device regulatory requirements (21 CFR 820, EU MDD/MDR, ISO 13485:2016 and IEC 60601 series) related to design control and process/product goals (e.g., process capability, yield, reliability) are met utilizing project planning and execution skills.
Identify and manage needs/requirements and assist with the creation and/or modification of product and process specifications
Lead design transfer activities focused in development of gage design, inspection processes, GR&R, capability studies and process validation
Actively participate in Design Review activities of new products and work closely with product design teams to manage quality considerations during all PLM stages of product development
Provide guidance and work to solve significant or chronic process or product problems. Discuss customer concerns or complaints with Marketing and Sales as needed
Generate, analyze, and present reports on quality related Key Performance Indicators (KPIs) such as line yields, final release, supplier performance and customer experiences to internal product improvement teams
Support Quality Systems such as delivery holds, internal and external audits, CAPA and investigations
Update and revise procedures to consistently meet regulatory requirements such as EU MDR, IEC 60601 series, ISO 13485:2016, 21 CFR 820, etc.
Analyze and act on process trend data including leading investigations, root cause analysis and assist with corrective actions.
Hold oneself and others accountable to conduct business in a manner compliant with Bioventus’ Code of Compliance and Ethics, policies and procedures and internal controls applicable to their role.

What you'll bring to the table

Bachelor’s degree (Masters preferred), in an Engineering discipline or equivalent technical background, with emphasis or experience in electronics, circuits and/or software. Electrical Engineering or related fields preferred.
Minimum 5 years (with Bachelor’s) or 4 years (with Master’s) of experience within the medical device industry with a comprehensive understanding of, and ability to interpret regulations and guidelines governing medical devices including ISO 13485 and 21 CFR 820 and EU MDD/MDR.
Strong working knowledge of process and product development and validation methodologies (IQ,OQ,PQ).
Experience interacting directly with suppliers, Manufacturing, and Manufacturing support organizations.
Understanding and experience in applying quality engineering concepts such as process capability analysis, risk management, PFMEA and DFMEA.

Are you the top talent we are looking for?

Apply now! Hit the “Apply” button to send us your resume and cover letter.

Bioventus is committed to fostering an inclusive and diverse community of employees with a strong sense of belonging. We believe we are bettered by all forms of diversity and take pride in working with top talent from every walk of life. In the spirit of inclusivity, qualified applicants will be considered without regard to age, ethnicity, disability, gender, veteran status, gender expression, gender identity, nationality, race, religion or sexual orientation. All individuals, regardless of personal characteristics, are encouraged to apply.

Apply Now

Refine Your Search

senior validation engineer jobs in memphis tn

Sr Quality Engineer

Senior Process Engineer - MSAT

Senior Data Engineer

Senior Mechanical Design Engineer

Manufacturing Engineer I, II or Sr.

Senior Image Data Scientist-Center for Bioimage Informatics

Senior Software Engineer

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