Material Handler

AVEVA DRUG DELIVERY SYSTEMS INC•Miramar, FL

21h•Onsite

About The Position

Assists in the packaging and clinical labeling of Aveva’s transdermal and transmucosal products by handling and transferring raw materials, packaging components, and equipment parts. This role also involves assisting in other packaging processes for Aveva’s products once primary packaging activities are complete. Key responsibilities include verifying raw materials, staging components, meticulously following Batch Record and SOP instructions, and completing all required documentation. The Material Handler will also document operational parameters, manage packaging waste, provide components during packaging, close, label, palletize, and transport finished goods. Daily tasks include weighing and documenting component weights, performing standard testing procedures, and using a pallet jack for transportation. The position requires cleaning packaging rooms, equipment, and production areas, supporting clinical labeling operations, and strictly complying with current Good Manufacturing Practices (cGMPs), Standard Operating Procedures (SOPs), and safety policies. The individual is expected to operate in accordance with the company's Code of Conduct and Business Ethics, adhere to all established regulatory, compliance, and safety requirements, and perform all work in support of corporate values: Innovate, Evolve, and Excel, while working as a member of a team.

Requirements

High school diploma or general education development (GED) credential.
Minimum of 1 year of related experience and/or training in Manufacturing/Packaging (pharmaceutical manufacturing, food manufacturing or general commercial manufacturing); or equivalent combination of education and experience.
Ability to read English and interpret documents such as safety rules, Standard Operating Procedures batch records and cleaning procedures.
Ability to write in English and complete batch record documentation.
Ability to speak English effectively.
Ability to add, subtract, multiply and divide in all units of measure, using whole numbers, common fractions and decimals.
Ability to compute rate, ratio, percent and to plot and interpret data graphically.
Ability to apply common sense understating to carry out detailed written and oral instructions.
Knowledge of FDA, DEA, cGMPs, and SOPs related to job requirements.

Nice To Haves

Manufacturing/Packaging experience in a GMP environment will be a plus.

Responsibilities

Verifies current raw materials for batches and stages components and dedicated equipment parts for each batch.
Follows all Batch Record and SOP instructions and completes all relevant documentation as required.
Documents operational parameters and steps performed in the batch record.
Documents and dispose of all packaging waste on a per shift basis and at the end of each batch.
Provides components as needed during the packaging of batches.
Closes, labels, palletizes and transports finished goods.
Weighs and documents the weight of components.
Performs standard testing procedures on daily basis.
Uses a pallet jack to transport finished goods and components.
Cleans packaging rooms and equipment, and any production area as needed and documents it in appropriate logbooks.
Supports clinical labeling operations as required.
Complies with current Good Manufacturing Practices, Standard Operating Procedures and safety policies while performing all job duties.
Maintains and cleans manufacturing and production areas and equipment per SOP requirements.
Operates in accordance with our Code of Conduct and Business Ethics, and all established regulatory, compliance and safety requirements.
Performs all work in support of our corporate values: Innovate, Evolve and Excel.
Works as a member of a team to achieve all outcomes.
All other relevant duties as assigned.