Manager, Packaging Engineering

Integra LifeSciences•Columbia, MD

1d•$109,250 - $149,500

About The Position

Changing lives. Building Careers. Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care. The Packaging Engineer Manager is responsible for managing all aspects of the design, development, and validation of packages and packaging systems for medical devices at Tissue Technologies division of Integra, in compliance with applicable FDA and ISO requirements. This individual is responsible for providing departmental technical expertise for package development while collaborating with regulatory, marketing, market research, supply chain, process excellence and other affiliated departments and organizations to identify and address packaging needs. These duties include managing the strategy for the development of sterile barrier systems and secondary packaging, creating, and maintaining detailed specifications, creating, and executing validation/qualification protocols, and responsibility for packaging equipment selection and development, material selection, supplier selection, and labeling. SUPERVISION RECEIVED Manager provides regular oversight on task/ activities related to project deliverables and timeline. This position will be responsible for the career development of Packaging Engineers, technician and interns. SUPERVISION EXERCISED May oversee and provide task/ activity guidance to department engineers, interns, and lab technician.

Requirements

Minimum of a bachelor’s degree in Packaging Engineering or other engineering disciplines or possess the equivalent combination of education and experience.
Minimum of 10 years of experience developing and validating packaging systems for medical devices.
Expert knowledge of the U.S. and International standards governing the design, development, testing, and manufacture of medical devices, particularly ISO 11607, ISO 13485 well as ASTM and ISTA test methods and practices.
Expert knowledge of U.S. FDA, cGMP, and ISO requirements for the design, validation, manufacturing processes, secondary operations, and assembly of packaging systems
Manage direct reports through professional development
Ability to drive projects with tight timelines and drive them to successful completion.
Excellent verbal and written communication skills; ability to lead meetings and effectively present to a group
Demonstrate effective time management and verbal and written communication.
Critical thinking and problem solving to develop solutions
Knowledge of gamma, ETO, and e-beam sterilization methods
Proficient PC skills (MS Word, MS Excel, MS Project, MS Visio).

Nice To Haves

A master’s degree in Packaging Engineering or other engineering disciplines is preferred.

Responsibilities

Manage the design, development, and qualification of packages and packaging systems for sterile and non-sterile medical devices at Integra Lifesciences.
Lead cross functional teals while executing projects start to finish
Independently determine and develop approach to solutions and present results to peers and leadership.
Articulate and drive packaging strategy and develop the associated Standard Operating Procedures (SOPs) and best practices to ensure success and align to current regulations and business strategies
Establish timelines, budget estimates, and resource requirements for package development, sustaining and continuous improvement projects and drive the projects to successful completion
Mentor the Tissue Technologies R&D Packaging Engineering team members and provide project direction, prioritization, and technical oversight to ensure successful implementation of packaging strategy in support of product leadership goals.
Support the conceptualization, initiation, development and implementation of new packages and processes including design generation, prototyping, consumer acceptance testing, engineering specifications, verification and validation, and technology transfer
Identify and investigate industry best practices and implementation improvements as appropriate
Demonstrate technical expertise on packaging, materials, and processes along with the ability to communicate that knowledge to internal and external partners
Prepare and maintaining the departmental policies, procedures, and manuals
Investigate design changes and failures, product complaints, and non-conformances, report findings and recommendations in company systems for corrective and preventive action
Prepare Failure Mode Effects Analysis (FMEA) and risk assessments for products and processes
Process validations of new and modified designs and processes
Collaborate with Quality to ensure compliance to appropriate ISO/FDA regulations for the design, testing, documentation, and manufacturing of the company’s products
Interface with Manufacturing, Quality, Regulatory, Research & Development, Sales, Marketing, and outside vendors to accomplish assigned tasks
Perform other duties as assigned
Demonstrate a commitment to understanding packaging and labeling related global medical device manufacturing, ISO 13485, and regulations through active participation in company training as well as through self-education by reading related articles and attending seminars
Work effectively on computers using Microsoft Office and Minitab statistical software to collect data, create histograms and graphs, and write protocols and reports