Development Quality Engineer

Abbott; Los Angeles (CA); Presencial; USD 70 000 - 90 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Medical Plan

Dental Plan

Vision Plan

HSA

FSA

Life Insurance

Short-term Disability

Long-term Disability

401(k)

Resumo da oferta

Abbott is seeking a Development Quality Engineer to support design control, risk management, and product development processes. The role is onsite in Sylmar, CA for a 12‑month assignment.

Requires 1–2 years of experience and a bachelor’s degree in engineering or a related technical field. Responsibilities include leading quality deliverables, developing verification tests, maintaining DHF content, and ensuring regulatory compliance.

Qualificações

• Strong communication and teamwork abilities.
• Bachelor-level engineering or technical degree required.
• Experience as an individual contributor in quality.
• Good multitasking and organizational skills.

Responsabilidades

• Participate in or lead teams supporting quality disciplines and design control deliverables.
• Support on-time execution of Quality Plans for internal PDP development.
• Handle CPDP and design change projects for OEM-based products.
• Generate PDP design verification test plans/reports for product requirements.
• Lead or support risk management activities from concept through commercialization.
• Develop and maintain hazard analyses and risk assessments.
• Collaborate with design engineering on product requirements and verification/validation.
• Ensure DHF content completion and regulatory compliance.
• Identify and implement effective process controls and CAPA systems.

Conhecimentos

Verbal/written comms

Interpersonal skills

Independent contributor

Multitasking

Computer skills

Formação académica

Bachelor's degree in Engineering

Descrição da oferta de emprego

Title: Development Quality Engineer

Location: Sylmar, CA

Duration: 12 Months

100% Onsite

Years Experience:

• 1-2 years.

Skills:

• Verbal and written communication
• Interpersonal, teamwork
• Individual contributor
• Multitask, strong organizational
• Advanced computer skills

Education:

• Bachelor level degree in an Engineering Discipline or other technical field experience.

Duties:

• Participate in or lead teams in supporting quality disciplines, decisions, and practices, lead on-time completions of design control deliverables
• Support on-time execution of Quality Plans for internal product development process (PDP)
• OEM-based Clinical Product Development (CPDP) and design change projects
• Accountable for generation of PDP design verification test plans/reports for product/system requirements
• Lead or support Risk Management activities from product concept through commercialization
• Including generation of risk management plans/reports
• Completion and maintenance of hazard analysis
• FMECA's and Cybersecurity risk assessments
• Lead identification of essential outputs and generate Essential Output reports
• Accountable for completion of labeling verification activities and labeling verification reports
• Work with design engineering in the completion of customer/system/product requirements
• Work with design engineering in the completion of product verification and validation
• Endure DHF content completion
• Integrity and regulatory & standards compliance
• Collaboratively communication resolving gaps, complete document change request reviews in a timely and objective manner
• Identify and implement effective process control systems to support the development
• Qualification and on-going manufacturing of products to meet or exceed internal and external requirements
• Assist in the implementation of assurances
• Process controls and CAPA systems designed to meet or exceed internal and external requirements
• Assist in the development and execution of streamlined business systems which effectively identify and resolve quality issues
• Apply sound
• Systematic problem solving methodologies in identifying, prioritizing, communicating and resolving quality issues
• Support all company initiatives as identified by management and in support of quality management systems (QMS)
• Environmental Management Systems (EMS) and other regulatory requirements
• Additional duties may be identified by functional management based on the current project/business objectives.

Consultants Eligible Benefits Upon Waiting Period:

• Medical and Prescription Drug Plans
• Dental Plan
• Vision Plan
• Health Savings Account (for High-Deductible Health Plans)
• Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
• Supplemental Life Insurance
• Short Term Disability (coverage varies by state)
• Long Term Disability
• Critical Illness, Hospital coverage, Accident Insurance
• MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
• 401(k)

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.

Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.