Offer summary

Qualifications:

Bachelor's Degree, Experience in project management, transition activities.

Key responsabilities:

Drive global supply chain labeling strategy and implementation

Collaborate with global supply planning team

Manage pre and post inventory by sku and site globally

Coordinate with key stakeholders for supply strategy execution

Medical Device Industry Experience Required

Katalyst Healthcare's & Life Sciences (Katalyst HLS) is a Global Contract Research Organisation that provides End-to-End Clinical Research Services for Healthcare and Life Sciences companies globally. At Katalyst HLS offers ICH-GCP compliant clinical trial services from Phase I–IV in all key therapeutic areas to support clinical development and research requirements and also provides validation, quality and regulatory services for Pharma/Bio-Pharma/Medical Device industries. Services:- Clinical Trial Management- Clinical Data Management- Biostatistics & Statistical Programming- Medical Writing- Pharmacovigilance- Quality and Regulatory Affairs- GMP, GLP and GCP Validations- Manufacturing Process Validations- Equipments & Instruments Validations- Computer Systems Validations- Human Resourcing

Job description

Responsibilities:

Drive global supply chain labeling strategy and implementation/execution for labeling changes related to embecta separation activities.
Collaborate with global supply planning team to assess implementation needs and provide input into integrated management office to drive deliverables (i.e., lead times, prioritization of manufacturing plans, inventory builds etc.) .
Must be experienced in project management, transition activities and be able to influence cross-functional team and key stakeholders. Must also possess executive communication and have experience in global end-to-end supply chain with expertise in supply planning.
Scope includes management of pre and post inventory by sku and by site around the world (>400 finished good materials >18 distribution locations)
Coordination with manufacturing, regulatory, quality, and other key stakeholders as required to drive execution of supply strategy to maintain customer service levels.
Collaborate with global supply planning team to assess implementation needs and provide input into integrated management office to drive deliverables (i.e. lead times, prioritization of manufacturing plans, inventory builds etc.) .
Must be experienced in project management, transition activities and be able to influence cross-functional team and key stakeholders. Must also possess executive communication and have experience in global end-to-end supply chain with expertise in supply planning.
Scope includes management of pre and post inventory by sku and by site around the world (>400 finished good materials >18 distribution locations)
Coordination with manufacturing, regulatory, quality, and other key stakeholders as required to drive execution of supply strategy to maintain customer service levels.
Medical Device Industry Experience Needed.
Bachelor's Degree.