Job Functions1. Purchasing2. Shipping and Logistics3. Documentation and Administration4. Problem Solving and Analysis5. Communication and Collaboration
Job Requirements1. High School Diploma or Equivalent Combination of Education, Training, and Professional Experience2. Previous Experience in Purchasing3. Demonstrated Ability to Obtain Knowledge from Resources on Lean Six Sigma Methodologies and Proven Analytical/Problem Solving Capabilities4. Demonstrated Familiarity with Microsoft Programs like Word, Excel, PowerPoint, Project, Teams, Outlook, etc.5. Demonstrated Ability to Acquire Knowledge from Resources on Electronic Quality Management Systems such as MasterControl and Trackwise
Skills1. Lean Six Sigma Methodologies2. Microsoft Programs (Word, Excel, PowerPoint, Project, Teams, Outlook)3. Electronic Quality Management Systems (MasterControl and Trackwise)4. Pharmaceutical Industry Knowledge5. Analytical/Problem Solving Capabilities1. Energetic and SelfMotivated2. ResultsOriented and Efficient3. Creative and OpenMinded4. Ability to Work Well in a CrossFunctional Team Environment5. Good Communication Skills
Job Overview:
To provide a comprehensive & timely purchasing and shipping service.
Responsibilities:
- Issue and fill purchase orders.
- Assist in purchasing.
- Assist in handling shipping,
- Create packing lists & related documentation, including shipping labels (FedEx, UPS, etc.)
- Schedule truck pick up.
- 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.
- Previous experience in the pharmaceutical industry.
- Previous experience in purchasing.
- Demonstrate 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 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 ability to develop a good understanding 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 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).
27 To 32 (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>