Manufacturing Engineering Planning

Manufacturing Engineer
Lead, execute the project activities and collaborate with cross functional teams to support successful project delivery.
PPAP execution and documentation support, BOM and EIS updates, Manufacturing Procedure updates, inventory planning coordination, readiness tracking and reporting of all project deliverables.
Create Validation Master Plans, process validation protocols, and reports, ECN and non-ECN documents as needed to support the project.
Engineering study protocols and reports, prepared in accordance with project timelines and priorities established.
Change control assessments, work instructions, batch records, and related forms and other documents as needed, developed with appropriate inputs and training as provided by BD to ensure compliance and successful execution of deliverables.
Support the expansion of prefilled syringe filling and plunger insertion capacity through vendor sourcing, User Requirements Specifications (URS) development, capital requests, FAT/SAT execution, validation, and cross-functional project management.
Coordination with vendors for equipment design, procurement, and implementation.
Data collection and analysis for inspection processes across subassembly and finished goods.
Identification of redundant or non-value-added inspection steps
Collaboration with SMEs, Quality, and Operations to optimize inspection strategy
Support the manufacturing operations through process optimization, waste elimination, equipment validation, documentation updates, and cross-functional problem solving.
Factory Acceptance Test (FAT) protocols
Site Acceptance Test (SAT) protocols
Equipment and process validation protocols (IQ/OQ/PQ as applicable)

Lead and coordinate project meetings, track action items, and maintain project deliverables and timelines.
Updating documentation and supporting training activities

Support process improvement initiatives, including:
Validation of new or modified equipment to improve efficiency and throughput

Support engineering studies, data analysis, and technical documentation required for process, inspection, or equipment improvements.
Coordinate with manufacturing teams to secure line time and execute builds required for validation, testing, and process improvements.
Ensure all activities are executed in compliance with BD Quality System, GMP requirements, and applicable regulatory standards.
Technical Writing skills as applied to manufacturing documentation and process improvement - Experienced in the creation and revision of technical documentation.
Demonstrates the ability to follow established procedures according to Good Manufacturing Practices (GMP).
Minimum of 7 years of work experience in a manufacturing environment. Preferably in the high-volume production of medical devices. Experience in Manufacturing processes knowledge such as Castings, Injection Molding, Sheet Metal, welding, Machined components - Understands some fabrication methods, Sterilization Process and their applications.
Ability to represent functional and operations organization with clarity
Functional or cross functional liaison with stakeholders concerning operational or project deliverables.
Ability to manage customer satisfaction initiatives.
Experience in Food and Drug Administration (FDA) 21 CFR 820 and International Organization for Standardization (ISO); Experience in Lean Manufacturing initiatives with an emphasis in continuous improvement.
Experience in applying Manufacturing Statistical methods and statistical tools. Strong experience using Microsoft tools and SAP.
Proven ability to work independently and meet deadlines with no supervision.
Requires a bachelor’s degree in mechanical engineering or related field with 7 years of experience in a manufacturing engineering role.