Pharmaceutical Packaging Operator

Pharmaceutical Packaging Operator

Title: Pharmaceutical Packaging Operator (multiple openings)

Location: Tampa, FL

Industry: Pharmaceutical

Hours: 7AM - 3:30PM (M-F)

Salary: $20/HR.

Employment Type: Long-term contract with the possibility to go perm

Environment

This client is one of the world s leading suppliers to the pharmaceutical, biotech, and specialty ingredients markets. We create products that support a healthier lifestyle and enhance one s quality of life.

Overview

Operates and tends machine that performs one or more packaging functions, such as filling, marking, labeling, tying, packing, or wrapping containers.

Summary

One will execute assembly instructions per Batch Record requirements for packaging and labeling processes in compliance with cGMP guidelines. This will require on time and neat documentation during the execution to assure compliance. Provide support to the Manufacturing Group, QA, Warehouse and Facility operations by complying with company and FDA cGMP requirements.

Responsible for the performance of cleaning of Primary and Secondary Packaging rooms and Packaging equipment. This will include the corresponding Room Sanitizations per Departments procedures.

Responsibilities

Follow batch record instructions in the execution of manual process for Primary and Secondary Packaging as applicable.

Assist in the operation and set-up of automated equipment in the performance of certain primary or secondary packaging operations.

Assist in the reconciliation and movement (Chain of custody) of materials between packaging areas and the warehouse.

Report any observations to QA, Team Lead, Equipment Specialist CPS Project Coordinator or Manager of potential issues that could result in deviation or investigation.

Perform Cleaning and Sanitization of Primary and Secondary Packaging rooms.

Support the Equipment Specialist in the execution of qualification protocols for new equipment as assigned.

Training on SOPs to remain current for job requirements, logbook entries and GMP documentation.

Attend applicable meetings, discussions, etc., in support of these projects to meet the Production Schedule.

Participate in safety processes and meetings as applicable.

Maintain a positive, professional and confidential relationship with sponsors. Comply with all state and federal regulatory requirements and guidelines.

Adhere to all defined Safety and Sustainability requirements and expectations and seek clarification whenever Safety and Sustainability requirements and expectations are either unknown or unclear

Promptly report identified Safety and Sustainability issues, problems, deficiencies, errors, incidents, and/or opportunities to manage and correct where possible

Stop work where deemed necessary to maintain safety

Required Qualifications

1-3 Years experience in a pharmaceutical GMP environment

HS Diploma or GED required

Steel-toe boots are required for this role

SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire, and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to match professionals rapidly and precisely to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.

EOE/ADA

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