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Warehouse Associate

Pii (Pharmaceutics International, Inc.)
Hunt Valley, MD Full Time
POSTED ON 7/25/2024 CLOSED ON 8/23/2024

What are the responsibilities and job description for the Warehouse Associate position at Pii (Pharmaceutics International, Inc.)?

Job Overview

Handling warehouse materials and maintaining documentation.

Responsibilities

  • Raw material staging.
  • Assist in the receiving process, including labeling, and the transfer of materials from wooden to plastic skids.
  • Assist in the receiving process by delivering supplies to appropriate parties.
  • Scan movement of materials in the Warehouse Management System (WMS)
  • Complete cGMP documentation, including material transfer forms.
  • Ensure picking order forms are complete and a copy accompanies the kit being transferred.
  • Ensure kits are prepared on time, are accurate and verified by another associate.
  • Follow cleaning procedures and maintain the cleaning logbook.
  • Maintain supply cages without clustering of materials.
  • Cycle Counting Inventories as needed.
  • Perform other duties as assigned.

Qualifications

  • High school diploma, or equivalent combination of education, training and professional experience that provides the individual with the required knowledge, skills, and abilities.
  • Pharmaceutical warehouse experience helpful
  • Obtain and maintain forklift certification.
  • Demonstrate the ability to obtain the appropriate knowledge from resources on Lean Six Sigma Methodologies and proven analytical/ problem solving capabilities.
  • Demonstrates the ability to establish good working relationships with other departments, including vendors, colleagues, and subordinates.
  • Demonstrates the appropriate technical knowledge necessary to make sound decisions on development issues with minimal supervision.
  • Demonstrate the ability to analyze data and information and assess and resolve complex problems/issues as required.
  • Must be able to comprehend and follow all applicable SOPs.
  • Demonstrate the ability to acquire the appropriate knowledge from resources on electronic Quality Management Systems such as MasterControl and Trackwise.
  • Demonstrate the ability to acquire the appropriate knowledge from resources on the current federal, local, and international regulations regarding the production, testing, and release of drug substances and products.
  • Demonstrate the ability to acquire the appropriate knowledge from resources on cGMPs, industry, and regulatory standards and guidelines.
  • Demonstrate familiarity with Microsoft programs like Word, Excel, PowerPoint, Project, Teams, Outlook, etc.
  • Demonstrate the ability to portray the appropriate level of integrity and professionalism.
  • Demonstrate the ability to communicate effectively with management, staff, regulators, and client representatives in written and verbal formats.
  • Demonstrate the ability to complete tasks accurately and according to established and shifting timelines.
  • Demonstrate the ability to make quality scheduling, resource allocation, and priorities decisions.
  • Energetic, execution-focused, self-motivated, and organized individual who is accustomed to working in a deadline-focused, high-pressure entrepreneurial environment.
  • Results-oriented and efficient.
  • Creative and open-minded who fosters an environment in which sharing of ideas is encouraged.
  • Demonstrate the ability to work closely with a diverse customer and employee base (internally and externally).
  • Demonstrate the ability to work well in a cross-functional team environment.
  • Must communicate fluently in English and have legible handwriting.

Physical Demands

  • Ability to push or pull 1,000-pound pallets safely.
  • Ability to travel between and within facilities to visit staff, operations, and projects, as needed.
  • Ability to sit, stand, climb stairs, and climb ladders to mezzanines (when necessary).
  • Ability to lift up to 40 pounds on occasion.
  • Ability to use PPE (safety shoes, goggles, respirators, gloves, etc. when necessary).
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