Product Quality Engineer

Roles & Responsibilities

• Leads and develops a team of quality engineers supporting manufacturing process quality oversight, validation, qualification, and compliance activities.
• Provides functional leadership for quality engineering activities across manufacturing processes, equipment, utilities, facilities, and associated systems.
• Provides technical direction for quality engineering matters related to base business operations, development, tech transfer, and market expansion projects.
• Ensures validation and qualification strategies, protocols, reports, and lifecycle activities are executed in accordance with Client Quality Systems, cGMP requirements, and applicable regulations.
• Reviews quality and compliance gaps related to manufacturing processes, equipment, utilities, systems, and change controls, and drives appropriate risk-based actions.
• PARTNERS WITH MANUFACTURING, VALIDATION, ENGINEERING, REGULATORY, QUALITY SYSTEMS, AND DEVELOPMENT TO SUPPORT COMPLIANT IMPLEMENTATION OF NEW AND EXISTING PROCESSES.
• GUIDES RISK MANAGEMENT ACTIVITIES, INCLUDING ASSESSMENTS, MITIGATION PLANNING, AND APPLICATION OF QUALITY RISK MANAGEMENT PRINCIPLES.
• OVERSEES OR SUPPORTS QUALIFICATION AND VALIDATION ACTIVITIES FOR EQUIPMENT, PROCESSES, CLEANING, UTILITIES, COMPUTERIZED SYSTEMS, AND METHODS, AS APPLICABLE.
• ENSURES QUALITY ENGINEERING ISSUES IMPACTING PRODUCT QUALITY, PROCESS ROBUSTNESS, AND REGULATORY COMPLIANCE ARE IDENTIFIED, ESCALATED, AND RESOLVED.
• COMMUNICATES QUALITY ENGINEERING STATUS, KEY RISKS, TRENDS, AND RECOMMENDATIONS TO MANAGEMENT AND EXECUTIVE STAKEHOLDERS, AND MANAGES FUNCTIONAL RESOURCES AND BUDGET TO SUPPORT EFFICIENT EXECUTION.

Education & Experience

• Minimum Bachelor's degree required preferably in Physical or Life Sciences, Pharmacy, or Engineering.
• Certified Quality Engineer or formal training in quality engineering or statistics is preferred.
• 8+ years of combined experience in Manufacturing, QA, QC, R&D in pharmaceutical, biologics, device or chemical industry.
• 4+ years of supervisory/technical leadership experience.
• MUST HAVE A BASIC UNDERSTANDING AND WORKING KNOWLEDGE OF THE PHYSICAL AND CHEMICAL CHARACTERISTICS OF THE PRODUCTS, INCLUDING RAW MATERIALS, MANUFACTURED AT THE PLANT.
• MUST BE FAMILIAR WITH USE OF STATISTICAL QUALITY SYSTEMS, ELECTRONIC DOCUMENT MANAGEMENT AND LABORATORY INFORMATION MANAGEMENT.
• MUST ALSO BE FAMILIAR WITH QUALITY POLICIES AS WELL AS cGMP AND OTHER REGULATORY REQUIREMENTS.
• MUST HAVE EFFECTIVE PEOPLE MANAGEMENT AND COMMUNICATION SKILLS NECESSARY TO SUPERVISE THOSE REPORTING DIRECTLY OR THROUGH SUBORDINATES AS WELL AS ESTABLISH AND MAINTAIN EFFECTIVE WORKING RELATIONSHIPS AMONG OTHER KEY INDIVIDUALS IN MANUFACTURING, MATERIALS MANAGEMENT, ENGINEERING, PRODUCT DEVELOPMENT, QUALITY SYSTEMS, PRODUCT QA, QUALITY CONTROL, INFORMATION SYSTEMS AND REGULATORY AFFAIRS AND MUST DEMONSTRATE SOUND JUDGMENT IN EVALUATING AND ACTING ON DAY-DAY SITUATIONS.
• BACHELOR'S, MASTER'S OR PHD IN A LIFE SCIENCE OR ENGINEERING IS HIGHLY DESIRED.
• DEMONSTRATED STRATEGIC VISION AND LEADERSHIP IN BUILDING AND SUSTAINING A HIGH-PERFORMING TEAM RESPONSIBLE FOR MANAGING BASE BUSINESS PRIORITIES, SITE-RELATED PROJECTS, COMPLIANCE REMEDIATION ACTIVITIES, AND GLOBAL PROJECT DELIVERABLES IS HIGHLY DESIRED.
• STRONG CROSS-FUNCTIONAL COLLABORATION AND NEGOTIATION SKILLS, WITH THE ABILITY TO INFLUENCE STAKEHOLDERS, ALIGN PRIORITIES, AND DRIVE EFFECTIVE OUTCOMES ACROSS COMPLEX AND DIVERSE FUNCTIONAL TEAMS IS HIGHLY DESIRED.