Manufacturing Supervisor (2nd/3rd Shift)

Augustbioservices; Nashville (TN); On-site; USD 90,000 - 120,000; Full time

Job summary

August Bioservices in Nashville, TN is seeking a Manufacturing Supervisor to lead the new aseptic formulation and filling facility. You will manage equipment prep, filling, packaging, and ensure production schedules align with site goals.

This role reports to the Manager of Manufacturing Operations and requires 4+ years of cGMP manufacturing, a BS in pharma or equivalent, and strong leadership, communication, and problem-solving skills.

Qualifications

• 4+ years of cGMP manufacturing experience with supervisory duties.
• Bachelor’s degree or equivalent pharma manufacturing experience.
• Must qualify in Aseptic Grade A/B gowning.
• Experience operating aseptic equipment and HMI controls.
• Strong problem solving, data synthesis, and deviation investigations.
• Able to work flexible hours and communicate effectively.
• Self-starter who can work independently.
• Excellent MS Word/Excel/PowerPoint/Outlook skills.

Responsibilities

• Accountable for production activities spanning equipment preparation, formulation, filling, packaging and related processes.
• Oversee manufacturing schedule and development of team and KPIs.
• Provide training, coaching, mentoring and discipline to team members.
• Set goals for team to align with site and company objectives.
• Lead deviation assessments and implement CAPAs.
• Drive change controls for process improvement and CAPAs.
• Develop on‑the‑job training plans for the manufacturing team.
• Ensure personnel are qualified with cGMP requirements and procedures.
• Maintain cleanroom environments to cGMP requirements.
• Develop department goals and budget aligned with site goals.
• Develop cross‑functional knowledge to support operations as needed.

Skills

cGMP knowledge

Supervisory experience

Problem solving

Communication skills

Team player

Flexible hours

Independent worker

Education

Bachelor’s degree or equivalent pharma manufacturing experience

Tools

Microsoft Word

Excel

Outlook

PowerPoint

Job description

Headquartered in Nashville, TN, August Bioservices is a high‑growth Contract Development Manufacturing Organization (CDMO) focused on drug discovery, formulation, and manufacturing services across the biopharma sector.

Role Overview

The Manufacturing Supervisor will lead the manufacturing team at the Nashville, TN site, contributing to the buildout and qualification of a new aseptic formulation and filling facility. This role reports to the Manager of Manufacturing Operations.

Responsibilities

• Accountable for production activities spanning equipment preparation, formulation, filling, packaging and other related processes. Primary container platforms include vials, syringes, bags and tubes.
• Responsible for execution of the manufacturing schedule and oversight and development of the team and related KPIs.
• Provides training, coaching, mentoring and discipline to team members to ensure development as individuals contributing to the goals of the department and company.
• Sets goals for team members to deliver the vision of the manufacturing operation aligned with site and company objectives.
• Leads deviation assessments and implements corrective actions (CAPAs).
• Drives change controls for process improvement or changes and CAPAs.
• Establishes requirements and develops on‑job training plans for the manufacturing team.
• Ensures personnel are qualified and proficient with applicable cGMP requirements and internal governing procedures.
• Maintains cleanroom environments to cGMP requirements.
• Develops and manages departmental goals and corresponding budget in alignment with the corporate and site goals.
• Expected to develop cross‑functional knowledge and qualify on processes to support operations as needed.

Qualifications

• 4+ years of cGMP manufacturing experience; previous supervisor experience preferred.
• Bachelor’s degree is preferred or equivalent pharma manufacturing experience.
• Must be able to qualify in Aseptic Grade A/B gowning.
• Ability to operate equipment utilized in aseptic operations, including HMI controls.
• Comprehensive knowledge of cGMP regulatory requirements for aseptic manufacturing.
• Demonstrated ability to troubleshoot, solve problems, synthesize data, summarize outcomes and provide recommendations on a compliant path forward, and own deviation investigations.
• Demonstrated ability to successfully execute responsibilities in a fast‑paced environment, collaborating across corporate functions and multiple stakeholders.
• The ability to work flexible hours on short notice due to manufacturing demand.
• Self‑starter and ability to work independently.
• Strong written and verbal communication and presentation skills.
• Team player with well‑developed interpersonal skills and excellent organizational skills.
• Excellent computer skills in Microsoft Word, Excel, Outlook, and PowerPoint.

Shift Schedule

• 1st Shift: 7:00 am – 3:30 pm (Monday – Friday)
• 2nd Shift: 3:00 pm – 11:30 pm (Monday – Friday)
• 3rd Shift: 11:00 pm – 7:30 am (Sunday – Thursday)
• Weekend Day Shift: 7:00 am – 7:00 pm (Saturday – Monday)
• Weekend Night Shift: 7:00 pm – 7:00 am (Friday – Sunday)

ADA Accommodation Notice

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Physical Requirements

• 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.

EEO Statement

August Bioservices is an equal‑opportunity employer and values diversity. All aspects of employment, including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs. August Bioservices does not discriminate on the basis of any status protected under federal, state, or local law.