Posted in Other about 2 hours ago.
Location: REMOTE
Description:
Description:
The Supply Chain Serialization Senior Associate is a key role responsible for ensuring consistent high performance and reliability of the serialization systems and processes. The role requires a strong focus on driving quality into operations and continuous improvement. The senior associate will support key serialization and traceability projects and efficiently aid with GMP document creation, project management, reporting and problem resolution, while adhering to compliance and regulatory guidelines.
Key Responsibilities:
Support cross-functional Track & Trace projects from beginning to end.
Support and transform existing business models by leveraging innovative technologies to drive organizational value, performance, decision-making and patient experience
Support implementation of compliance driven regulations.
Preferred Qualifications:
Relevant experience in biopharmaceutical operations or Supply Chain
Understanding of / experience in Operations, including Supply Chain, Manufacturing, Engineering
Experience with common supply operations systems, such as SAP ATTP or similar systems
Experience working in a GMP environment
Familiarity with Serialization and Global Track & Trace regulations (e.g., US DSCSA, EU FMD, etc.)
Knowledge of GS1 standards and guidelines (e.g. EPCIS)
Ability to communicate and collaborate cross-functionally in an organization
Ability to manage multiple projects concurrently
Maintain procedures and compliance with serialization regulations in a timely fashion
Basic Qualifications
Master's degree or Bachelor's degree and 2 years of experience or Associate's degree and 6 years of experience or High school diploma / GED and 8 years of experience
Top 3 Must Have Skill Sets:
Experience in working cross functional teams
Relevant experience in Supply Chain, Distribution
GMP work experience to support GMP documents, and processes
Day to Day Responsibilities:
The senior associate will support key serialization and traceability projects and efficiently aid with GMP document creation, project management, reporting and problem resolution, while adhering to compliance and regulatory guidelines.
McKesson |
BIOTRONIK, Inc. |
Williams Lea |