Quality Engineer from Apidel Technologies

Duration: 0-18 month(s)
Shift Timing: 8:00 AM - 5:00 PM

Job Responsibilities:

• Work closely with Operations and the business functions to ensure quality performance of product and processes.
• Collaborate with Internal cross-functional and Supplier teams to address top quality issues.
• Own identified internal and supplier-driven Non-Conformances (NC) and Corrective Action Preventative Action records (CAPA), managing the timely processing and closure of NC and CAPA records within the electronic management system, Trackwise.
• Support execution and analysis of manufacturing related complaint investigations and product field actions.
• Investigate and disposition internal non-conforming product within MRB, issuing NCs as appropriate.
• Communicate & collaborate with suppliers regarding non-conformances, escalating Supplier Corrective Action Requests (SCAR) as required.
• Execute and manage Supplier Initiated Change Requests (SICRs) received from suppliers, engaging with cross-function teams for assessment and approval.
• Support manufacturing transfers to/from other plants/facilities, executing appropriate quality activities.
• Collaborate with appropriate stakeholders to identify and execute opportunities for supplier part certification.
• Process Improvements/Validation.
• Engage in the development and improvement of the internal manufacturing and distribution processes for existing products.
• Perform critical assessments and qualifications of internal and supplier-proposed change management activities, including Production Part Approval Process (PPAP) activities for supplier changes.
• Participate in and potentially lead the creation and/or review of new or modified procedures.
• Support the development and review of process and equipment validation/qualification and MSA of internal processes.
• Maintain KPIs for monitoring of process and/or product quality, perform analysis, and interpret trends, identifying and activating on appropriate actions as necessary.
• Perform other related duties as assigned.
• Minimum of 3 years of experience
• CAPA Experience
• Top 3 Skills (Multi-tasking, Strong communication and Problem-Solving)
• Systems - TrackWise/ERP Systems experience, MS Suite Experience
• Power BI knowledge is a PLUS but not required
• Strong quality background with CQE and/or LSSGB or LSSBB certification
• Previous medical device industry experience desired with an understanding of US and International Medical Device Regulations, familiarity with ISO 13485, GDP, and GMP as well as experience interacting with regulatory agencies (FDA, MoH, TUV, etc.) and working in compliance risk situations.
• Strong knowledge of and experience with key Quality concepts (e.g. Risk Management, CAPA, Audits, Statistics, DMAIC, DFSS).
• Strong project management, leadership, and influencing skills as well as the ability to manage multiple tasks simultaneously.
• Demonstrated ability to successfully manage and complete projects in a matrix organization as well as to work independently and as part of cross-functional teams.
• Ability to represent Quality function within project teams.
• Strong interpersonal skills, written communication, oral communication, and negotiation skills.
• Highly-developed critical, problem-solving, analytical, and "outside the box" thinking.
• Ability to work in a fast-paced, dynamic, and time-critical manufacturing environment.
• Strong computer literacy (Excel, Databases, ERP Systems, TrackWise, Statistical software packages, etc.)