Packaging Operator

Aequor; Tampa (FL); On-site; USD 21,878 - 31,159; Full time

Job summary

A reputable pharmaceutical company in Tampa is seeking a Production Operator to manage production lines and ensure compliance with quality and safety standards. The role requires a High School degree and 1-year manufacturing experience, preferably in a GMP environment. Candidates must be detail-oriented, able to work shifts up to 12 hours, and physically capable to meet job demands.

Qualifications

• 1 year of manufacturing experience in a high-speed production environment.
• Experience in a GMP regulated environment preferred.
• Ability to work any shift up to 12 hours.

Responsibilities

• Manage production lines to meet the established production schedule.
• Comply with safety regulations and conduct activities safely.
• Operate high-speed equipment for assembly, filling, and packaging.

Skills

Detail-oriented

Manual dexterity

Math skills

Effective communication

Teamwork

Education

High School degree or equivalent

Tools

Microsoft Office

SAP

Job description

Overview

Duration: Contract till Nov 2026 with possibility to extend

Pay rate: $19.25/hr on W2

Job Summary:

• Manage production lines to meet the established production schedule in accordance with Standard Operating Procedures (SOPs) and Good Manufacturing Principles (GMPs) while monitoring product to ensure quality standards are maintained.
• Comply with all safety regulations and conduct all activities in a safe, efficient manner.
• Apply 5S and cGMPs in all areas of responsibility.
• Operate high-speed equipment for the manual or automated assembly, filling, packaging and labeling of pharmaceutical products: ensuring adherence to specifications.
• Perform tasks that may be verified by an independent individual; or perform inspection/verifications of work performed by others.
• Clean packaging rooms and machinery in accordance with SOPs and cGMPs.
• Conduct Set-Ups, in-process actions, data entry, and other computer-related tasks.
• Complete batch records accurately and documents production volumes in accordance with SOPs and cGMPs.
• Accept or reject products according to acceptability standards determined by cGMPs, customer requirements, and SOPs.
• Complete Line Clearances and Change-Overs on production lines in accordance with SOPs and cGMPs.
• Conduct in-process inspections and reconcile incoming and completed components and products to ensure accuracy and accountability.
• Perform other duties as assigned.
• Incumbent has full authority to make decisions and/or take action that is required to carry out job duties. Internal requirements include compliance with ethics, environmental health and safety, financial, human resources, cGMP procedures, general business policies, requirements and objectives. The incumbent must be willing to take temporary assignments as required.

Regulated Responsibilities (including cGMP and EHS):

• Incumbent is expected to be fully compliant with all criteria established by governmental agencies, Ministry of Health, and legislative requirements including, but not limited to: the FDA, European Community (EC), ISO 13485 - Medical Devices, European Economic Community Medical Device Directive (MDD), Canadian Medical Device Regulations (CMDR), OSHA, Sarbanes-Oxley, EPA, DOT, EEOC, and ADA.
• Incumbent will work to ensure that the company is in compliance with all environmental, health and safety requirements and assure our business practices enhance the welfare of our customers, employees and the community in which we operate. The incumbent must be willing to take temporary assignments as required.

Education and Experience

• Education: High School degree or equivalent with one year of manufacturing experience.
• Technical experience: One (1) year related work experience, preferably in a high-speed production or manufacturing environment.
• Regulatory experience: Experience working in a GMP regulated environment preferred.
• Systems experience: Basic user knowledge of Microsoft Office, SAP experience preferred.
• Aseptic experience: Experience working in an Aseptic Production environment preferred.

Desired Skills and Qualifications

• Detail-oriented and self-motivated
• Excellent hand-eye coordination and manual dexterity
• Excellent math skills; ability to add, subtract, multiply, and divide
• Ability to read, comprehend, write, and communicate effectively in English
• Ability to carry out detailed written or oral instructions
• Ability to work and communicate with others in a professional and effective manner, within a team-oriented environment
• Basic user knowledge and understanding of Windows-based computer systems such as Microsoft Office, with an ability to learn other computer-based systems
• Ability to work any shift (up to 12-hours) as required dependent on business needs
• Physically able to continuously stand and walk
• Ability to work in a controlled environment and comply with gowning requirements such as: hairnets, beard covers, safety shoes, goggles and/or safety glasses
• Ability to interpret work instructions and standards of work independently
• Physically able to lift up to 40 lbs. for men and 35 lbs. for women
• Physically able to bend, climb, lift, squat, stoop, and stretch to reach frequently
• Effective and efficient operation of manual and automated production equipment
• Ability to use, clean, and store tools and other devices required for the performance of the job in a manner which prevents damage to the tools and / or equipment

Please contact me if you are interested. Thank you.

Thank You,

Gurpreet Kaur

Aequor Technologies LLC

377 Hoes Lane, Suite 300

Piscataway, NJ 08854

[phone]

Seniorit y level

• Associate

Employment type

• Contract

Job function

• Other

Industries

• Manufacturing, Pharmaceutical Manufacturing, and Medical Equipment Manufacturing

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