Job Description

Production Operator (GMP)

Coral Springs, FL 33065

Shifts:1st shift and 2nd shift

Temp to perm

Job Summary: As a Production Operator, you will play a vital role in the manufacturing, labeling, and packaging of medical drug products. You will be responsible for ensuring that production processes run smoothly, safely, and efficiently, adhering to the highest standards of quality and compliance.

Job Responsibilities:

Operator I:

• Verify dispensed raw materials for batches and stages components.
• Assemble production equipment for each batch and perform equipment daily usage checks.
• Follow and understand all Batch Record and SOP instructions while completing relevant documentation.
• Document all operational parameters and steps in the batch record for manufacturing and packaging.
• Perform standard in-process testing procedures daily.
• Monitor production lines for accuracy, stability, conformity, and product defects.
• Stage and distribute components for manufacturing and packaging batches.
• Place product into shipper boxes and attach shipping labels.
• Document and dispose of all production waste in dedicated waste containers at the end of each batch.
• Transport finished goods using carts or pallet jacks, including moving in and out of refrigerated coolers.
• Clean production rooms and equipment, documenting tasks in logbooks.
• Support Laboratory and QA operations as needed.
• Work safely as part of a team to achieve all outcomes.
• Operate in accordance with company values, including Collaboration, Courage, Perseverance, and Passion.
• Perform major and minor GMP room cleaning tasks.
• Perform all other relevant duties as assigned.

Operator II:

• Perform compounding activities, including delicate equipment setup.
• Troubleshoot minor equipment issues and make in-process adjustments to maintain operating parameters.
• Assist in coaching and mentoring Level I operators as needed.
• Execute all Operator I functions.
• Perform all other relevant duties as assigned.

Job Requirements:

• Computer literacy is required
• High school diploma or GED equivalent.
• Minimum of six months of experience and/or training, or equivalent combination of education and experience within a production cGMP environment.
• Knowledge of FDA cGMP, GDP, and SOPs.
• Ability to read, interpret, and complete documentation in English.
• Proficiency in basic math skills, including the ability to use different units of measure and calculate averages.
• Ability to apply common sense and follow detailed instructions.

Physical Requirements and Working Conditions:

• Must be able to sit, stand, walk, stoop, kneel, crouch, or crawl for at least 8 hours.
• Ability to frequently lift and/or move up to 50 pounds.
• Exposure to varying temperatures (2°C to 25°C) and moving mechanical parts.
• Potential exposure to fumes, airborne particles, toxic, and/or caustic chemicals (PPE Provided).
• Must be able to wear personal protective equipment (PPE) such as respirators, jumpsuits, eye, and hearing protection.
• May require additional hours, including weekends, depending on operational needs.

ttg Talent Solutions is an Equal Opportunity Employer and recruiting agency. We are committed to creating an inclusive and diverse work environment and welcome applications from all qualified candidates regardless of race, color, religion, gender, sexual orientation, national origin, age, disability, or veteran status. Please note that all offers of employment are contingent upon the successful completion of a drug test and background check. We maintain a drug- and substance-free workplace to ensure the safety and well-being of all employees.

At ttg, "We believe in making a difference One Person at a Time," ttg OPT.

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