Acadia Pharmaceuticals Inc. Princeton , NJ 08544
Posted 2 weeks ago
Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average.
The Sr. Analyst is responsible for overseeing and driving key commercial, clinical and non-commercial logistics and supporting related manufacturing operation activities (GMP and non-GMP). He/she will coordinate and track critical logistics activities. Develop and manage critical internal logistics and supply chain processes and support key supply operation functions including Trade Compliance readiness. Ensure up-to-date and accurate data to support supply chain and logistics shipment requirements and supply operations targets.
Primary Responsibilities
Develop and appropriately scale critical supply chain, logistics and operations processes
Support development of Acadia's logistics operations for GMP products, including development of robust processes and systems to track, manage, and communicate all logistics activities.
Support commercial and non-commercial GMP and non-GMP logistics and supply operation and shipment activities and develop shipping lane routing guides.
Coordinate key development material shipments with Acadia managed carriers utilizing existing business processes, carrier portals and supply chain tools. Create shipping documents, customs invoices and other required logistics documents.
Coordinate shipments of Acadia commercial, non-commercial and clinical goods, and as required, internal shipment requests.
Support identification and management of Acadia's domestic and international contract storage warehouse's for Acadia commercial and clinical materials.
Tracking and updating shipments utilizing Smartsheet and other business tools and following up with vendors to complete chain of custody paper works for shipments.
Support trade compliance policies and procedures with shipment import/exports.
Assist/participate in creation of key processes, Dashboards, flow diagrams and work instructions across key departments and participate in relevant meetings.
Other duties as assigned.
Education/Experience/Skills
Requires a Bachelor's degree in business or scientific related field. Targeting 4 years of progressively responsible experience in GMP pharmaceutical logistics and/or supply chain materials management. An equivalent combination of relevant education and experience may be considered.
Demonstrated experience developing with GMP logistics operations, systems and procedures preferably with a virtual pharmaceutical company
Experience in utilization of ERP based systems a plus
Strong experience developing scaling critical supply chain processes (Create Flow diagrams and author Work Instructions)
Strong interpersonal skills with experience working with multiple contract service providers
Experience with GMP and temperature sensitive products
Strong analytical and computer skills required. Proficient in MS office tools including Powe Bi, Adobe functions and Smartsheet a plus
Knowledge of CMO contract relationships, purchase orders and planning activities
Strong negotiating skills and problem solving abilities
Strong attention to detail, process oriented, organizational and Good Documentation Practices skills
Ability to identify and understand what needs to be accomplished and able to drive activities independently
Effective oral and written communication skills including ability to write technical reports and communicate with senior management and subject matter experts (SMEs) as well as CMO supply chain, customs brokers, carriers agents and project management teams
Ability to manage change in a dynamic environment
Skilled at creating a team environment that supports a common vision and ability to work cross functionally within multi-departmental teams within and without the organization
Proficiency at effectively prioritizing goals, assessing team capability, and coordinating resources to achieve those goals
Ability to travel 10% of the time both domestically and internationally
Physical Requirements
While performing the duties of this job, the employee is regularly required to stand; walk; sit; use hands to finger, handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, see, talk or hear in a standard office environment and independently from remote locations. Employee must occasionally lift and/or move up to 20 pounds. Ability to travel independently overnight and work after hours if required by travel schedule or business needs.
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Acadia Pharmaceuticals Inc.