Production Lead - Pharmaceutical Manufacturing

Ttg Talent Solutions; Florida; On-site; USD 70,000 - 100,000; Full time

Job summary

ttg Talent Solutions is seeking a Production Lead to support pharmaceutical manufacturing in a cGMP-regulated environment. This on-site role blends hands-on production with documentation and compliance responsibilities, including batch records, SOPs, and GMP adherence.

Based in Coral Springs, FL, the position is full-time, Monday through Friday, with a temp-to-perm path. Pay is Based on Experience, reflecting expertise and performance in batch manufacturing, quality control, and production

Qualifications

• 5+ years of experience in pharmaceutical manufacturing in a cGMP-regulated environment.
• Experience with Batch Records, SOPs, cGMP, and GDP.
• Hands-on exposure to manufacturing equipment, filling, packaging, compounding, or production processes.
• Experience with deviations, change controls, qualification documentation, or QMS documentation.
• Experience with SAP, QMS, MES or similar systems.
• Knowledge of inhalation, or respiratory manufacturing.
• Strong attention to detail, communication, teamwork, and problem-solving skills.

Responsibilities

• Support batch manufacturing, compounding, filling, and packaging operations.
• Set up, operate, inspect, and clean production equipment according to SOPs.
• Complete and review Batch Records, logbooks, in-process records, cleaning records, and other production documentation.
• Verify raw materials, components, equipment, and production quantities.
• Perform and document in-process checks to ensure product quality and compliance.
• Prepare or support SOPs, deviations, change controls, protocols, qualification documents, and other GMP documentation.
• Ensure manufacturing activities comply with cGMP, GDP, SOPs, and FDA requirements.
• Support equipment checks, calibration records, troubleshooting, and production readiness.
• Work closely with Production, QA, QC, Warehouse, and Maintenance to resolve issues and meet production goals.
• Maintain accurate documentation and communicate production or quality issues promptly.

Skills

5+ years experience

Manufacturing equipment

Deviations

Change controls

Qualification documentation

QMS

Inhalation manufacturing

Attention to detail

Communication

Teamwork

Problem solving

Tools

SAP

QMS

MES

Job description

Production Lead - Pharmaceutical Manufacturing

03rd November, 2026

Location: Coral Springs, FL

Work Arrangement: On-site

Schedule: Full-Time | Monday - Friday

Type of Contract: Temp-to-Perm

Pay Rate: Based on Experience

Position Overview

ttg Talent Solutions is seeking an experienced Production Lead to support pharmaceutical manufacturing operations in a cGMP-regulated environment. This position combines hands-on production activities with manufacturing documentation and compliance responsibilities. The ideal candidate will have experience in pharmaceutical manufacturing, production equipment, batch records, SOPs, and GMP.

Key Responsibilities

• Support batch manufacturing, compounding, filling, and packaging operations.


• Set up, operate, inspect, and clean production equipment according to SOPs.


• Complete and review Batch Records, logbooks, in-process records, cleaning records, and other production documentation.


• Verify raw materials, components, equipment, and production quantities.


• Perform and document in-process checks to ensure product quality and compliance.


• Prepare or support SOPs, deviations, change controls, protocols, qualification documents, and other GMP documentation.


• Ensure manufacturing activities comply with cGMP, GDP, SOPs, and FDA requirements.


• Support equipment checks, calibration records, troubleshooting, and production readiness.


• Work closely with Production, QA, QC, Warehouse, and Maintenance to resolve issues and meet production goals.


• Maintain accurate documentation and communicate production or quality issues promptly.

Qualifications

• 5+ years of experience in pharmaceutical manufacturing in a cGMP-regulated environment.


• Experience with Batch Records, SOPs, cGMP, and GDP.


• Hands-on exposure to manufacturing equipment, filling, packaging, compounding, or production processes.


• Experience with deviations, change controls, qualification documentation, or QMS documentation is highly valued.


• Experience with SAP, QMS, MES, or similar manufacturing systems is a plus.


• Knowledge of inhalation, or respiratory manufacturing is highly preferred.


• Strong attention to detail, communication, teamwork, and problem-solving skills.

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

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