Packaging Engineer - Technology Transfer

Virbac•Bridgeton, NJ

22h•Onsite

About The Position

Virbac Animal Health is seeking a Packaging Engineer - Technology Transfer to join our Manufacturing Science & Technology (MSAT). The Packaging Engineer works as a key technical resource in supporting company objectives with respect to packaging and labeling component design, engineering support and project management. The position supports manufacturing by assisting in troubleshooting, investigations and operational improvement initiatives. The position will also lead capital improvements and provide project engineering support. This position will work cross-functionally with various departments to effectively address product and process cGMP readiness for manufacturing, planning, and coordination.

Requirements

Bachelor’s degree (or equivalent) in a science or engineering discipline
3-5 years of experience in packaging engineering or packaging process development.
At least 2 years in a Pharmaceutical / FDA regulated environment
Working knowledge of cGMP standards and experience working in a regulated environment
Proven analytical thinking and problem-solving skills
Demonstrated success operating in cross-functional teams
Strong verbal, written and interpersonal communication skills
Strong organizational and computer skills
Prior experience using lean and six sigma principles and tools.
Ability to travel up to 10% of time

Responsibilities

Lead and support packaging process, labeling and component improvement
Develop and maintain packaging and component databases.
Support risk assessments with key cross functional stakeholders and set up the control strategy.
Determines and coordinates physical testing to ensure product and package integrity for manufacturing through end users.
Participate in core team meetings and ensure collaboration with cross-functional stakeholders.
Develop and execute engineering studies to qualify packaging components, processes and equipment.
Basic ability to modify existing packages by taking them from the bench, pilot plant and commercial scale based on customer or consumer needs.
Ability to create packaging material specifications providing technical information necessary to support the product/packaging configurations; to ensure projects deliver at efficient cost, line performance, package quality, supply chain requirements, and consumer satisfaction.
Develop and maintain the packaging processes, systems, procedures, test methods, and component specifications required to assure compliance with all packaging-related requirements.
Manage multiple projects and be able to focus and prioritize on important projects.
Ensure robust, efficient, and compliant packaging components, labeling and processes
Lead packaging engineering studies to introduce new and improved packaging materials, techniques and/or technologies
Create scale up models by developing expert processing equipment understanding and characterization at different scales.
Evaluate packaging and components to support cost savings and change initiatives.
Provides technical leadership of equipment, automation and/or facility improvement projects
Utilize technical packaging knowledge to support root cause problem solving.
Provide solutions based on risk and benefit assessments using basic problem analysis and resolution, statistical methods, and design of experiments tools.
Prepares engineering evaluations and test plans for and executes modification change control documentation.
Packaging process, material and equipment understanding, control, and capability
Develop packaging engineering documentation and support GMP manufacturing
Author and review GMP-critical documentation, such as experimental reports, batch records, process work instructions, development and technology transfer reports.
Support GMP product and process investigations including deviations, change controls and CAPAs.
Complete manufacturing process reviews of processes intended for technology transfer, highlighting critical process parameters and critical material attributes.
Write and/or review CMC regulatory documents.
Guarantee proper documentation for training and compliance requirements