Position Brand Description:
This position manages master data at the Branchburg NJ site utilizing established processes and serves as a key technical resource at the operational level. This position drives master data solutions and ensures master data maintenance processes lead to consistent and accurate master data (materials, BOMs, recipes, resources) for site and supply chain operations.
Key Objectives/Deliverables:
Manage for Results /Strategic Planning:
- Leads key data maintenance and data design for master data in SAP, DSP, and associated systems.
- Defines and maintains formal Standard Operating Procedures, policies, and training materials.
- Determines impact of local and /or global changes while ensuring global data consistency and conformance to established site and global policies.
- Contributes to global initiatives for Master Data Management as required and participates in select power user forums to share best practices with peers.
- Leverage appropriate tools and reports to track maintenance efforts and data accuracy.
- Leads costing, quality, warehouse, and supply chain master data meetings and drives reviews of key master data fields.
- Troubleshoots SAP execution problems (which could include logging formal IT incidents), identifying root causes, and implementing solutions.
- Investigates master data deviations and provides impact assessments for change management.
- Work with TS/MS, Manufacturing and Supply Planners to create and maintain up to date Super BOMs to ensure uninterrupted supply of materials for all manufacturing campaigns.
- Create and maintain Materials, BOMs, Resources & Recipes within SAP for all molecules at Branchburg site.
- Support MES rollout at Branchburg as a core team member to define master data requirements.
- Support and abide by applicable Compliance policies, Corporate Integrity Agreement, FDA, CGMP, HSE and other policy and procedure documents. All corporate and cGMP, HSE compliance training requirements must be met as required and defined.
Basic Requirements:Â
- 3-5 years experience in FDA-regulated industry, working in commercial/clinical manufacturing environment.
- Good analytical skills to collect, organize production plan from multiple source systems to identify any potential constraints.
- Ability to work independently, and on multiple concurrent project initiatives is necessary.
- Must be a team player, self-motivated and collaborate ideas and solutions effectively with management and colleagues.
- Proficiency in MS Office Applications a must, including the use of Microsoft Excel.
- Excellent verbal and written communication skills are essential for this position.
Additional Preferences:Â
- Functional expertise within SAP, such as Materials Management is desirable.Â
Education Requirements:Â
- Bachelor’s degree in a scientific field or equivalent (i.e., supply chain, computer systems, engineering, science preferred) or equivalent work experience.
This role is exempt and the anticipated compensation for this role is $64,500 - $104,000.
This is a banded role, and candidates will be placed within the range based on experience, skills, internal equity, and market considerations.
Celltrion Branchburg, LLC offers a comprehensive benefits package that includes paid time off (holidays, vacation, and additional leave), medical, dental, and vision insurance, life insurance, a company-matched retirement savings plan, wellness programs, and short- and long-term disability benefits. This role requires up to 10% travel, on-call availability, and may involve shift work. Hybrid work flexibility may be available based on business needs; relocation assistance is not provided.Â
Celltrion Branchburg, LLC is proud to be Equal Opportunity Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity or expression, national origin, protected veteran status, disability, or any other legally protected status.
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