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August Bioservices

US-based CDMO for end-to-end drug development

Visual Inspector 1 - 2nd & 3rd Shift

Inspection & TestUpdated on Nov 7
Full-timeNashville, TN, USANo salary listedIn-person

About the Job

Requirements

  • A high school diploma or equivalent is required.
  • Basic math skills are required to perform batch calculations.
  • Must be able to visually detect defective vials and maintain visual inspection qualification requirements.
  • At least 1 year of experience working in a pharmaceutical or other Good Manufacturing Practice-regulated environment is required.
  • Good documentation and communication skills and strong attention to detail are required.
  • Strong mechanical skills and learning agility are required.
  • Must be able to work in a team and in a fast-paced collaborative environment.
  • Must be able to work overtime when required.
  • Must be able to sit for prolonged periods while working at a desk and computer and lift up to 15 pounds at times.

Responsibilities

  • Visually inspect products for various defects.
  • Accurately and contemporaneously document work on batch records and protocols.
  • Set up and operate inspection equipment.
  • Perform line clearance activities.
  • Calculate inspection results and reconcile batches.
  • Minimize production downtime through advanced troubleshooting.
  • Assist Maintenance personnel with preventive maintenance and calibration activities.
  • Communicate professionally with supervisors, coworkers, managers, and clients.
  • Follow relevant Standard Operating Procedures and work instructions.

Desired Qualifications

  • Previous sterile packaging, clinical trial packaging, or related manufacturing experience is preferred.

About the Company

August Bioservices

US-based CDMO for end-to-end drug development

August Bioservices is a US-based CDMO that provides end-to-end drug development and manufacturing from preclinical to commercial stages. It manages all steps in a single program, including research, development, testing, laboratory services, and sterile fill/finish, while following cGMP standards. It differentiates itself with a hybrid model that combines large-CDMO scale and capabilities with a strong focus on customer service and integrated workflows. Its goal is to help clients bring safe and effective drugs to market efficiently by delivering comprehensive development and manufacturing under one roof.

Company size
51-200
Company stage
Series B
Total funding
$88.6M
Headquarters
Nashville, TN
Founded
2017

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