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Labeling In Pharma Jobs in Tennessee (NOW HIRING)

Batchmixer II

Bristol, TN ยท On-site

$16.50 - $20.25/hr

Collects the blend granulation into appropriate clean containers that are properly labelled and ... experience in a manufacturing environment, preferably Pharma/GMP manufacturing environment.

Batchmixer II

Bristol, TN ยท On-site

$16.50 - $20.25/hr

Collects the blend granulation into appropriate clean containers that are properly labelled and ... experience in a manufacturing environment, preferably Pharma/GMP manufacturing environment.

Batchmixer II

Bristol, TN

$16.50 - $20.25/hr

Collects the blend granulation into appropriate clean containers that are properly labelled and ... experience in a manufacturing environment, preferably Pharma/GMP manufacturing environment.

Batchmixer II

Bristol, TN ยท On-site

$16.50 - $20.25/hr

Collects the blend granulation into appropriate clean containers that are properly labelled and ... experience in a manufacturing environment, preferably Pharma/GMP manufacturing environment.

Packaging Technician

Nashville, TN ยท On-site

$16.50 - $20/hr

... pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical ... Perform set-up and operations of packaging equipment, such as labelers, carton equipment, and ...

Packaging Technician

Nashville, TN

$16.50 - $20/hr

... pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical ... Perform set-up and operations of packaging equipment, such as labelers, carton equipment, and ...

Packaging Technician

Nashville, TN ยท On-site

$16.50 - $20/hr

... pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical ... Perform set-up and operations of packaging equipment, such as labelers, carton equipment, and ...

Showing results 21-40

Labeling In Pharma information

What is the difference between Labeling In Pharma vs Packaging Technician?

AspectLabeling In PharmaPackaging Technician
CredentialsHigh school diploma or equivalent; GMP training often requiredHigh school diploma or equivalent; GMP and safety training
Work EnvironmentCleanroom settings, pharmaceutical manufacturing facilitiesManufacturing lines, production areas
Industry UsageSpecifically in pharmaceutical labeling and complianceGeneral packaging across various industries, including pharma
Job FocusApplying labels accurately, ensuring regulatory complianceAssembling, packing, and preparing products for shipment

Labeling In Pharma involves precise application of labels in sterile, regulated environments, focusing on compliance. Packaging Technicians handle broader packaging tasks, often in less regulated settings. Both roles are essential in pharmaceutical manufacturing but differ in scope and specific responsibilities.

What is labeling in the pharmaceutical industry?

Labeling in the pharmaceutical industry involves creating and applying labels to medication packaging that include important information such as drug name, dosage, instructions, warnings, and expiration date. Pharmaceutical labeling professionals ensure compliance with regulatory standards and accuracy to support safe and effective use of medications.

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Technical Writer / Validation Documentation Consultant

Nashville, TN โ€ข On-site

Contractor

Re-posted yesterday


Job description

Position: Technical Writer / Validation Documentation Consultant
Location: Tennessee
Duration: 3–6 Months

Job Overview

The Technical Writer / Validation Documentation Consultant will support pharmaceutical cGMP packaging operations by developing and maintaining compliant technical and validation documentation for packaging processes, equipment, components, and new product introductions.

Key Responsibilities

  • Develop product-specific Master Batch Records (MBRs), Master Setup Sheets, Work Instructions, and controlled manufacturing documentation.
  • Prepare validation protocols, test scripts, and qualification documentation.
  • Develop and support FAT, SAT, Engineering Studies, IQ, OQ, and PQ documentation.
  • Design equipment- and component-specific validation tests.
  • Support execution of validation and qualification protocols as required.
  • Support label requests, labeling accuracy, traceability, and serialization-related changes.
  • Assist with new product introductions and packaging/component evaluations.
  • Support Change Controls, Deviations, CAPAs, Risk Assessments, and Root Cause Investigations.
  • Collaborate with Engineering, Quality, Operations, Production, Validation, and Technical Services teams.
  • Ensure documentation meets GMP, FDA, customer, and internal requirements.
  • Support continuous improvement and documentation standardization activities.

Required Qualifications

  • Pharmaceutical cGMP experience is required.
  • Hands-on technical writing experience in a pharmaceutical, biotech, or regulated GMP manufacturing environment.
  • Direct experience authoring validation and qualification documentation.
  • Experience with FAT, SAT, Engineering Studies, IQ, OQ, and/or PQ protocols.
  • Experience developing or maintaining Master Batch Records, manufacturing instructions, Master Setup Sheets, Work Instructions, or similar controlled documentation.
  • Understanding of equipment and process validation within pharmaceutical manufacturing or packaging operations.
  • Experience developing equipment- and component-specific validation tests.
  • Experience supporting validation or qualification protocol execution is strongly preferred.
  • Familiarity with packaging equipment, manufacturing processes, or new product introductions.
  • Knowledge of FDA and GMP documentation requirements.
  • Experience with Change Controls, Deviations, CAPAs, Risk Assessments, and Root Cause Investigations is preferred.
  • Strong technical writing, attention to detail, organization, and communication skills.
  • Ability to collaborate with Engineering, Quality, Operations, Production, and Validation stakeholders.
  • Proficiency with Microsoft Word, Excel, Teams, and Office 365.
  • Bachelor’s degree in Engineering, Life Sciences, Pharmaceutical Sciences, Technical Writing, or a related technical/scientific discipline is preferred. Relevant pharmaceutical cGMP and validation experience may be considered in lieu of a specific degree.