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August Bioservices

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

Filling/Formulation Manufacturing Technician - Weekend Shift

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeNashville, TN, USANo salary listedIn-person

About the Job

Requirements

  • A high school diploma or equivalent is required.
  • At least 1 year of experience in pharmaceutical manufacturing environments is required.
  • Mechanical aptitude to operate and troubleshoot a variety of equipment and instruments is required.
  • Understanding of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) is required.
  • Attention to detail and the ability to follow standard operating procedures and complete documentation tasks accurately are required.
  • Basic computer skills and familiarity with technical documentation are required.
  • Mathematical skills for measurements and calculations, including volume and weight, are required.
  • The ability to raise arms overhead, stoop, stand, climb, and lift 30–50 pounds is required.
  • Effective verbal and written communication skills are required.
  • The ability to stand, walk, or work in a cleanroom environment for prolonged periods is required.
  • The ability to wear fully protective gowning for extended periods is required.
  • The ability to lift and transport materials weighing up to 50 pounds is required.
  • The ability to consistently arrive at work on time for assigned shifts is required.
  • The ability to safely wear and work in a powered air-purifying respirator (PAPR) hood and associated equipment weighing approximately 2–3 pounds during assigned tasks is required.
  • The ability to perform sustained physical activities, including standing, walking, bending, reaching, lifting, and handling manufacturing equipment while wearing respiratory protection and personal protective equipment (PPE), is required.
  • The ability to wear and operate a PAPR for up to 4–6 hours per shift while performing manufacturing, equipment cleaning, and sanitization activities is required.
  • The ability to wear required PPE, including pharmaceutical gowning, respiratory protection, safety glasses, chemical-resistant gloves, and additional protective equipment as operational and safety procedures require, is required.

Responsibilities

  • Perform routine cleaning and sanitization of production areas to maintain a controlled and compliant environment.
  • Prepare and transfer materials and components for production using proper sanitization techniques and aseptic handling practices.
  • Use proper aseptic techniques in Grade B, C, D, and CNC environments during all tasks.
  • Adhere to safety and environmental health standards, including proper use of PPE.
  • Inspect, label, and package vials, IV bags, and syringes.
  • Dispense and formulate raw materials for aqueous and non-aqueous products, ensuring accuracy and compliance with batch records.
  • Prepare equipment for use with sterilization equipment such as autoclaves and HEPA cabinets.
  • Operate and maintain equipment used across formulation, filling, sterilization, inspection, and packaging processes, with support and oversight from other Manufacturing team members.
  • Complete GMP documentation, including batch records, protocols, and deviations, in accordance with Good Documentation Practices.
  • Collaborate with production, quality assurance, quality control, engineering, validation, and maintenance teams as required.
  • Recognize and report deviations, potential issues, or equipment malfunctions to the management team.
  • Load, operate, and unload sterilization equipment, including autoclaves, terminal sterilizers, and HEPA transfer carts.
  • Maintain a consistent presence on the Manufacturing floor and support production teams as needed.
  • Assist with setting up and operating filling lines and associated equipment, including mixers, tanks, pumps, autoclaves, and HEPA transfer carts.
  • Assist with troubleshooting equipment breakdowns.
  • Complete training for routine cleaning and sanitization of production areas.
  • Complete training to prepare and transfer materials and components for production using proper sanitization techniques and aseptic handling practices.

Desired Qualifications

  • An associate degree in a technical field is preferred but not required.
  • A bachelor's degree in biological sciences, chemical sciences, or engineering is preferred but not required.

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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