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).
21 To 26 (USD) Hourly
Life at Pharmaceutics International
Pii (Pharmaceutics International, Inc) is a multinational contract formulation and pharmaceutical development, Clinical Trial Materials (CTM), and commercial manufacturing company with corporate headquarters in Hunt Valley, Maryland, USA. Founded in 1994, Pii manufactures a wide range of dosage forms covering solid, semi-solid and aseptic filling. This service is complemented by full analytical and regulatory support.
Thrive Here & What We Value- Collaborative work environment that fosters sharing of ideas- Diverse customer and employee base (internally and externally)- Emphasis on quality standards and compliance with regulatory requirements- Adheres to Pii policies and procedures in carrying out maintenance assignments achieving excellence in timeliness, quality of work, documentation, inspection, and communicating skills.- Responsible for following all relevant regulations (e.g., FDA, OSHA, EPA, etc.)- Demonstrates ability to comprehend and follow all applicable SOPs- 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)- Ability to work well in a cross-functional team environment- Energetic, execution-focused, self-motivated, and organized individual who is accustomed to working in a deadline-focused, high-pressure entrepreneurial environment- Demonstrates excellent personal organizational skills.- Selfmotivated and team-oriented with the ability to work with minimal supervision and limited direction.- Can accommodate nonroutine work schedules, and be able to respond to call-ins.- Good understanding of cGMPs, industry, and regulatory standards and guidelines.</s>