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August Bioservices

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

Manufacturing Supervisor

Machine & Process OperationConfirmed live in the last 24 hours
Full-timeNashville, TN, USANo salary listedIn-person

About the Job

Requirements

  • At least 4 years of cGMP manufacturing experience.
  • Must be able to qualify in Aseptic Grade A/B gowning.
  • Ability to operate equipment used in aseptic operations, including human-machine interface (HMI) controls.
  • Comprehensive knowledge of cGMP regulatory requirements for aseptic manufacturing.
  • Ability to troubleshoot, solve problems, synthesize data, summarize outcomes, provide recommendations on a compliant path forward, and own deviation investigations.
  • Ability to execute responsibilities in a fast-paced environment while collaborating across corporate functions and multiple stakeholders.
  • Ability to work flexible hours on short notice due to manufacturing demand.
  • Ability to work independently.
  • Strong written, verbal, and presentation skills.
  • Excellent computer skills in Microsoft Word, Excel, Outlook, and PowerPoint.
  • Ability to safely wear and work in a powered air-purifying respirator (PAPR) hood and associated equipment weighing approximately 2 to 3 pounds during assigned tasks.
  • Ability to perform sustained physical activities, including standing, walking, bending, reaching, lifting, and handling manufacturing equipment while wearing required respiratory protection and personal protective equipment (PPE).
  • Ability to wear and operate a PAPR for extended periods, up to 4 to 6 hours per shift, while performing manufacturing, equipment cleaning, and sanitization activities.
  • Ability to wear required PPE, including pharmaceutical gowning, respiratory protection, safety glasses, chemical-resistant gloves, and additional protective equipment as required by operational and safety procedures.

Responsibilities

  • Accountable for production activities spanning equipment preparation, formulation, filling, packaging, and related processes, with primary container platforms including vials, syringes, bags, and tubes.
  • Execute the manufacturing schedule and oversee and develop the team and related key performance indicators (KPIs).
  • Train, coach, mentor, and discipline team members to support their individual development and departmental and company goals.
  • Set goals for team members aligned with the manufacturing operation's vision and site and company objectives.
  • Lead deviation assessments and implement corrective and preventive actions (CAPAs).
  • Drive change controls for process improvements, process changes, or CAPAs.
  • Establish requirements and develop on-the-job training plans for the manufacturing team.
  • Ensure personnel are qualified and proficient with applicable cGMP requirements and internal governing procedures.
  • Maintain cleanroom environments to cGMP requirements.
  • Develop and manage departmental goals and the corresponding budget in alignment with corporate and site goals.
  • Develop cross-functional knowledge and qualify on processes to support operations as needed.

Desired Qualifications

  • Previous supervisor experience.
  • A bachelor's degree, or equivalent pharmaceutical manufacturing experience.

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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