Manufacturing / Operations Quality Engineer 2

Manpower San Diegoabout 2 months ago
San Diego, CA, United States
Hybrid
Full-time
Junior Level (1-3 years)

Job Description

Position Overview

This position is responsible for manufacturing and product Quality activities. This role is within Mfg/Ops Quality organization and is accountable for supporting day-to-day sustaining activities in a manufacturing environment. The position requires exceptional communication, interpersonal, and project management skills to effectively coordinate activities and deliver results. This position will have direct interaction with Manufacturing and Process Engineering groups to support manufacturing sustaining activities, continuous improvement, and manufacturing capacity expansion. It may also have quality oversight for more than one manufacturing area and be responsible for supporting change management activities, nonconformances, equipment lifecycle, meeting facilitation, and other ad hoc sustaining manufacturing requests.

Key Responsibilities

  • Responsibilities: Provide ongoing quality engineering support throughout the product life cycle.
  • Responsibilities: Support engineering and manufacturing functions for validation planning and transfer activities, and assist teams in determining validation needs and requirements.
  • Responsibilities: Ensure adequacy of non-conformances and QI/CAPA records, investigations, and corrective actions.
  • Responsibilities: Support process risk management activities and ensure quality and completeness of validation packages and change orders.
  • Responsibilities: Become familiar with the applicable technology to facilitate participation in technical discussions and risk-based decision making.
  • Responsibilities: Review verification and validation reports and identify gaps for GMP compliance.
  • Responsibilities: Develop and execute strategies to close gaps in an efficient, technical, and compliant manner.
  • Responsibilities: Coordinate issue resolution using a risk-based approach.
  • Responsibilities: Ensure manufacturing processes and validation programs meet requirements of FDA and ISO.
  • Responsibilities: Trend, analyze, and report on quality data to improve product and process, and develop recommendations based on the data analysis.
  • Responsibilities: Collaborate with counterparts and cross-functional teams at other sites.
  • Responsibilities: Perform other activities as assigned.

Required Qualifications

  • Education: Bachelor’s degree in an engineering discipline.

Required Skills

Risk Management
FDA & ISO Compliance
Quality Engineering
Continuous Improvement
Validation & Verification
Nonconformance Analysis
Manufacturing Process Optimization
Project Management
Cross-Functional Collaboration
Change Management