Senior Manager Packaging Engineering; Hopewell, NJ

Position: Senior Manager Packaging Engineering (Hopewell, NJ)
## Senior Manager Packaging Engineering (Hopewell, NJ)
Apply locations:
Hopewell time type:
Full time posted on:
Posted Todayjob requisition :
R35071

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
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* General Description:

** Supporting Product commercialization for BeOne, the Senior Manager Packaging Engineering will have a main focus on our Hopewell, NJ manufacturing site, and responsible for commercial packaging qualification for drug substance, drug product, primary container/closure and final product presentations by:
* Utilization of standard processes in commercial development and lifecycle management of BeOne products in alignment with the overall manufacturing/packaging capability of BeOne operations at the Hopewell site as well as globally.
* Serving as the technical packaging lead in cross-functional teams including packaging site, supply chain, commercial, regulatory, finance, clinical, quality as well as across BeOne to commercialize products that create a successful patient experience.
* Assisting in the development of annual goals and strategic direction for the packaging organization aligning with the company overall strategy.
* Supporting product launches, tech transfers, and global expansion initiatives at our Hopewell site with packaging expertise.
* Ensure all packaging systems, equipment and processes comply with global regulatory requirements (e.g., FDA, EMA, etc.).
** Essential Functions of the Job:
*** Technical Support for the BeOne Hopewell, NJ, directing the design, supporting process, qualification, documentation and implementation of commercial packaging and thermal shipping solutions aligning with the product strategy including:  + Manage package development documents (technical drawing, specification, technical assessment, development protocol and report) utilizing the Veeva system.  + Develop and execute risk assessment, qualification plan, protocol, and summary report related to component qualification, packaging line testing, and temperature-controlled shipping system.  

+ Support HPW site in commercial launch and after launch efforts, packaging line qualification, pack design and specification, artwork, M  development, process improvement, and troubleshooting.
* Technical support for ongoing packaging activities at the Hopewell site, including process troubleshooting and support for new equipment initiatives.
* The pursuit of packaging technologies that will drive innovation and gain efficiency in packaging operations.
* Lead commercial packaging engineering activities in market launches and projects to meet predefined timeline and budget.
* Manage and execute change controls and deviations related to packaging.
* Author regulatory documents in support of product applications or provide regulatory filing and submission support.
* Accomplish goals within a team first environment and with respect for all members.
* Deliver progress reports and presentations ensuring that management is aware of the current status, progress, and future needs of projects and the organization.
* Identify and ensure area of responsibility complies with the most current standards and company policies.
** Education and Experience

Required:

*** Bachelor’s degree or and 7 years of Engineering experience or Master’s degree and 5 years of Engineering experience,
* Demonstrated experience leading teams, projects, programs or directing the allocation of resources preferably within the biotech, pharmaceutical, CRO, industry.
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* Supervisory Responsibilities:

*** Possibly intern supervision
** Computer

Skills:

** Proficient in Microsoft Office applications (Word, Excel, and Outlook), ERP Systems.
** Other

Qualifications:

** Understands comprehensive global pharmaceutical regulatory requirements (e.g. GMP, GDP). Due to global nature of company early morning or evening meetings may be required.
** Travel:
** Up to 20%
Global Competencies When we exhibit our values of Patients…