Senior Quality Engineer

Sr Engineer, Quality Engineering (Transfers)

Salary Range: $105,067 - $137,900

Financial compensation packages may be higher/lower than listed, & will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demand.

Support the transfer and manufacture of medical devices across multiple global sites. Collaborate with cross-functional professionals including, but not limited to, R&D, New Product Introduction (NPI), Design Quality Engineering (DQE), Product Quality Engineering (PQE), and Manufacturing to participate in and sustain the transfers of quality and manufacturing processes from New Product Development (NPD) and site-to-site for new and established medical devices.

What You'll be Doing

• Collaborate with cross functional engineers and professionals on developing, transferring, and sustaining robust quality and manufacturing processes, implement changes, including process improvements, and supporting projects across multiple global manufacturing sites.
• Participate as a key team member of projects in improving effectiveness and efficiency of established product lines.
• Participate and/or lead efforts to resolve product quality issues.
• Support and/or lead activities in various Quality Systems such as CAPA, Non-Conformance (NCR), equipment calibration, internal auditing, and quality metrics data analysis.
• Provide technical skill in many areas of quality engineering such as nonconformances, evaluating inspection data, evaluating process changes, implementing risk analysis, performing test method validations, and analyzing data.
• Work with Supplier Quality Manager/Engineers and suppliers as necessary.
• Support process and test method validation by developing, executing, or reviewing test protocols and reports.
• Coordinate implementation of new equipment and maintenance of existing equipment by reviewing equipment specifications and related qualification (IQ/OQ) reports and unscheduled maintenance reports.
• Support internal and external audits by participating in preparation activities and addressing audits findings.
• Work with R&D, Manufacturing Engineers, Regulatory, and Supply Chain Planners to support the transfers and implementation of new products into production or site-to-site.
• Work with R&D and Manufacturing Engineers to develop, review, and update risk analysis documents including product risk assessments and FMEA documents such as pFMEA.
• Provide technical direction to associates as needed to deliver on projects and assigned tasks.
• Meet goals with minimal supervision, lead projects, and manage multiple concurrent projects.

Required Qualifications

1. Bachelor’s degree in engineering or related field.
2. A minimum of four (4) years of quality and or manufacturing engineering experience in medical device or other regulated manufacturing industry.
3. Strong interpersonal and written and verbal communication skills.
4. Proficient computer skills including MS Word, Excel, Teams, Outlook, and statistical software (e.g., MiniTab).
5. Largely self-directed and proactively motivated.

Desired Qualifications

1. Ability to provide technical input to process development, design control, design verification and validation, process validation, test method validation, data analysis, risk analysis, and change control.
2. Strong knowledge of medical product quality assurance (including the requirements for test protocols, test reports, and statistical techniques).
3. Ability to comprehend rapidly evolving medical technologies and products.
4. CQE certification from reputable learning organizations is a plus.
5. Familiar and able to execute appropriate risk management tools.

EEO

We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, veteran status, marital status or any other characteristics protected by law.

Fair Chance Ordinance

If you are applying to perform work for Terumo Neuro in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Terumo Neuro reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.

Terumo Neuro will consider for employment qualified job applicants with arrest or conviction records in accordance with the California Fair Chance Act, Los Angeles County Fair Chance Ordinance for Employers, Fair Chance Initiative for Hiring Ordinance, and San Francisco Fair Chance Ordinance.