Production Lead - Pharmaceutical Manufacturing

ttg Talent Solutions, Inc.

Florida

On-site

USD 90,000 - 120,000

Full time

6 days ago
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Job summary

ttg Talent Solutions, Inc. is seeking an experienced Production Lead to support pharmaceutical manufacturing in a cGMP-regulated environment at our Coral Springs facility. The role blends hands-on production with documentation and compliance duties.

The ideal candidate will have GMP experience, batch records, SOPs, and equipment knowledge, and will collaborate with QA, QC, and maintenance to ensure product quality and regulatory readiness. This is an on-site, full-time position.

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, or production processes.
  • Experience with deviations, change controls, qualification documentation, or QMS documentation.
  • 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.

Responsibilities

  • Support batch manufacturing, compounding, filling, and packaging operations.
  • Setup, operate, inspect, and clean production equipment per 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

Attention to detail
Communication
Teamwork
Problem solving

Tools

SAP
QMS
MES

Job description

ProductionLead-PharmaceuticalManufacturing

ProductionLead–PharmaceuticalManufacturing

Location: CoralSprings,FL

WorkArrangement: On-site

Schedule: Full-Time|Monday–Friday

TypeofContract: Temp-to-Perm

PayRate: BasedonExperience

PositionOverview

ttgTalentSolutionsisseekinganexperiencedProductionLeadtosupportpharmaceuticalmanufacturingoperationsinacGMP-regulatedenvironment.

Thispositioncombineshands-onproductionactivitieswithmanufacturingdocumentationandcomplianceresponsibilities.Theidealcandidatewillhaveexperienceinpharmaceuticalmanufacturing,productionequipment,batchrecords,SOPs,andGMP.

KeyResponsibilities

  • Supportbatchmanufacturing,compounding,filling,andpackagingoperations.
  • Setup,operate,inspect,andcleanproductionequipmentaccordingtoSOPs.
  • CompleteandreviewBatchRecords,logbooks,in-processrecords,cleaningrecords,andotherproductiondocumentation.
  • Verifyrawmaterials,components,equipment,andproductionquantities.
  • Performanddocumentin-processcheckstoensureproductqualityandcompliance.
  • PrepareorsupportSOPs,deviations,changecontrols,protocols,qualificationdocuments,andotherGMPdocumentation.
  • EnsuremanufacturingactivitiescomplywithcGMP,GDP,SOPs,andFDArequirements.
  • Supportequipmentchecks,calibrationrecords,troubleshooting,andproductionreadiness.
  • WorkcloselywithProduction,QA,QC,Warehouse,andMaintenancetoresolveissuesandmeetproductiongoals.
  • Maintainaccuratedocumentationandcommunicateproductionorqualityissuespromptly.

Qualifications

  • 5+yearsofexperienceinpharmaceuticalmanufacturinginacGMP-regulatedenvironment.
  • ExperiencewithBatchRecords,SOPs,cGMP,andGDP.
  • Hands-onexposuretomanufacturingequipment,filling,packaging,compounding,orproductionprocesses.
  • Experiencewithdeviations,changecontrols,qualificationdocumentation,orQMSdocumentationishighlyvalued.
  • ExperiencewithSAP,QMS,MES,orsimilarmanufacturingsystemsisaplus.
  • Knowledgeofinhalation,orrespiratorymanufacturingishighlypreferred.
  • Strongattentiontodetail,communication,teamwork,andproblem-solvingskills.
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