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Manufacturing Supervisor, 1st Shift

Headquartered in Nashville, TN – one of the fastest-growing and most exciting cities in the United States – August Bioservices is a privately-owned, high-growth, and high-impact Contract Development Manufacturing Organization (CDMO).  As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our work is instrumental in helping to develop molecules today that can become the life-changing therapies of tomorrow. To support our growth plans, August is investing significant capital in a two-phase expansion project – including building a new state-of-the-art facility adjacent to our current facility. For those seeking dynamic opportunities, rewarding career paths and a chance to make a difference in global health, come grow with August!


The Manufacturing Supervisor is accountable and responsible for leading the 1st shift manufacturing team at the Nashville, TN site. This is an exciting opportunity to contribute to the buildout and qualification of a new manufacturing facility for Aseptic Formulation and Filling to establish a state of art manufacturing operation. The Manufacturing Supervisor will report to the Manager of Manufacturing Operations. The position will be located in Nashville, TN.


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 / changes or CAPAs
  • Establishes requirements and develops on-the-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.


Requirements
  • 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/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


At August Bioservices, Our Credo is our culture. Everything we do, we do with great care. We believe in the promise of discovery and the power of science to transform lives. We assert that excellence is not a static destination, but a standard, and an every-day measuring stick of our advancement. We aspire to unlock the potential in every person, every process and every molecule – from start to finish. We are committed to doing the right thing the first time and every time, meeting or exceeding all regulatory requirements. We strive to be exceptional, preferred and indispensable partners for our customers; responsible and engaged citizens within our communities; and active, mindful stewards of our environment.

 

We are August Bioservices. We are pointing the way forward. If this sounds like your kind of working environment, we want you on our team!


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.

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CEO of August Bioservices
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Average salary estimate

$70000 / YEARLY (est.)
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$60000K
$80000K

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What You Should Know About Manufacturing Supervisor, 1st Shift, August Bioservices

Are you ready to take your career to new heights? August Bioservices is seeking a talented Manufacturing Supervisor for the 1st Shift at our Nashville, TN facility. As part of our dynamic team, you'll play a pivotal role in the buildout and qualification of a state-of-the-art manufacturing facility dedicated to Aseptic Formulation and Filling. With over four years of cGMP manufacturing experience and a knack for leading teams, you'll oversee production activities including equipment preparation, formulation, filling, and packaging across various container platforms like vials, syringes, and bags. Your leadership will support the execution of the manufacturing schedule while fostering team development through training, coaching, and mentoring. We're looking for someone who's built to thrive in a fast-paced environment, possesses strong organizational and communication skills, and can bring innovative ideas for process improvements. At August Bioservices, we not only value your expertise but are also committed to your growth. Join us in our mission to transform lives through science and be part of a company that is truly making a difference in global health. If you’re self-motivated, ready for challenges, and eager to contribute to life-changing therapies, we'd love to meet you. Dive into this exciting opportunity and help shape the future of pharmaceutical manufacturing with August Bioservices!

Frequently Asked Questions (FAQs) for Manufacturing Supervisor, 1st Shift Role at August Bioservices
What are the main responsibilities of a Manufacturing Supervisor at August Bioservices?

As a Manufacturing Supervisor at August Bioservices, your primary responsibilities will include overseeing production activities encompassing equipment preparation, formulation, filling, and packaging. You'll also lead a team, ensuring they're well-trained in cGMP requirements and effectively managing manufacturing schedules, while driving process improvements.

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What qualifications are necessary for the Manufacturing Supervisor position at August Bioservices?

To be considered for the Manufacturing Supervisor role at August Bioservices, candidates should have at least 4 years of cGMP manufacturing experience, preferably in a supervisory capacity. A Bachelor’s degree is preferred, or equivalent industry experience, along with comprehensive knowledge of cGMP regulations and the ability to operate equipment in aseptic operations.

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How does August Bioservices support the development of its Manufacturing Supervisors?

At August Bioservices, we prioritize the professional growth of our Manufacturing Supervisors by offering training, coaching, and mentoring opportunities. You'll also set goals for your team to help them reach their full potential and contribute effectively to the company's objectives.

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What opportunities for career advancement exist for a Manufacturing Supervisor at August Bioservices?

Working as a Manufacturing Supervisor at August Bioservices can open numerous doors for career advancement. Our commitment to employee growth means you can move up within the organization as you foster skills like leadership and operational oversight while gaining experience in a cutting-edge manufacturing environment.

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What type of working environment can Manufacturing Supervisors expect at August Bioservices?

Manufacturing Supervisors at August Bioservices can expect a dynamic and engaging work environment where innovation is encouraged. We maintain a strong team-oriented culture focused on collaboration, professionalism, and compliance with all regulatory requirements, contributing to our mission of advancing global health.

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Common Interview Questions for Manufacturing Supervisor, 1st Shift
Can you describe your experience with cGMP manufacturing processes?

When answering this question, highlight your specific experiences in cGMP environments, including any roles where you've implemented or overseen processes that adhered to these guidelines. Be sure to illustrate how you stay updated on regulations and best practices.

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How do you handle conflicts within your team?

Discuss a specific example where you resolved a conflict or disagreement. Focus on communication, mediation techniques, and the importance of fostering a collaborative team environment at August Bioservices.

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What is your approach to team training and development?

You can express your understanding of the importance of continuous training in a cGMP environment at August Bioservices. Discuss methods you've used in the past to ensure your team remains knowledgeable and compliant, and how your training strategies align with the company's goals.

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Describe a process improvement you've implemented in your previous roles.

When prompted this question, share a detailed example of a successful process improvement project. Outline the steps you took, the challenges you faced, and the impactful results that came from your intervention.

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How do you ensure compliance with regulatory requirements?

Respond with your strategies for maintaining cGMP compliance, such as regular audits, staff training, and fostering an ethical work culture that values adherence to regulations at August Bioservices.

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What motivates you to work in manufacturing?

Share your passion for the pharmaceutical industry and the impact that manufacturing has on global health. Discuss specific aspects of the role that drive you, such as team dynamics, technology, and contribution to vital therapies.

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How do you prioritize tasks on a busy production day?

Explain how you assess the day’s priorities based on production schedules and team workload. Include examples of how you communicate these priorities to your team to ensure efficiency and accountability.

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What experience do you have with deviation investigations?

Share your experience in leading deviation investigations, including methods for identifying root causes and implementing corrective actions. This reflects your understanding of maintaining compliance within your team at August Bioservices.

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How do you manage your team’s performance and set clear goals?

Discuss techniques you've used to set performance indicators and monitor progress. Mention how you provide feedback and support to ensure team members reach their objectives and grow alongside the mission of August Bioservices.

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What are your thoughts on working under pressure in a manufacturing setting?

Express your perspective on the high-paced nature of manufacturing and how you thrive under pressure. Share past experiences where you effectively managed stress and kept your team focused on achieving production goals at August Bioservices.

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Full-time, on-site
DATE POSTED
April 3, 2025

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