Production Supervisor

Avantor; Paris (KY); On-site; USD 65,000 - 85,000; Full time

Job summary

Avantor in Paris, KY is seeking a Production Supervisor (Drys) to oversee the daily planning, implementation and maintenance of the manufacturing activities in a high-demand facility. The role requires strong leadership to drive safety, quality, and efficiency across shifts.

You will manage staffing, coordinate cross-functional activities, and enforce cGMP-compliant practices while advancing continuous improvements through data-driven approaches.

Qualifications

• Minimum 5 years of progressive manufacturing experience in a lean environment, with at least 1 year in a supervisory role.
• Strong leadership and people development skills.
• Excellent oral and written communication abilities.
• Experience with cGMP, SOPs and batch records is preferred.

Responsibilities

• Supervise manufacturing employees and coordinate activities across departments.
• Plan, schedule and coordinate staffing to fulfill orders and meet inventory targets.
• Ensure safety, quality, and compliance with documented procedures and work instructions.
• Lead continuous improvement efforts using data to optimize efficiency and reduce costs.
• Support audits and ISO-related activities and develop cross-training programs.

Skills

Leadership

Problem solving

Communication

Lean manufacturing

Risk assessment

Education

Bachelor’s degree preferred in a technical field

Job description

The Opportunity: Avantor is seeking a Production Supervisor (Drys) to oversee the daily planning, implementation and maintenance of the manufacturing activities of a specific area. The Production Supervisor ensures the effective use of materials, equipment and personnel in producing quality products at minimum costs. They select, develop, and evaluate personnel to ensure the efficient operation of the function and may assist higher level supervisors.

This is a full-time position based out of our Paris, KY location. Work Schedule: Monday-Thursday, 6am-4:30pm.

How you will thrive and create an impact: Supervise the activities of the manufacturing employees. May oversee the activities of other departments (production, maintenance, shipping). Plan, schedule, and coordinate departmental activities (including staffing) to fulfill sales orders, meet inventory requirements, and deliver manufactured products in accordance with established procedures and approved processes. Responsible for site security, safety and proper shutdown of site at conclusion of shift. Supervise and participate in the production operations. Monitor and improve the efficiency, output and safety of manufacturing processes through observations and measurements as well as by collecting and interpreting data. Ensures proper manufacturing processes are followed in accordance to written documentation (i.e., Batch Records, cGMPs, SOP's, Work Instructions). Maintains and revises procedures associated with production processes to ensure accuracy, consistency and product quality. Create, edit, and maintain necessary documentation (SOP's, Work Instructions). Ensure all manufacturing safety policies and procedures are implemented and maintained at all times. Investigates and eliminates departmental non-conformities in manufacturing processes by employing root cause analysis and implements corrective and preventative actions. Analyze and design lean manufacturing cells using effective systems to optimize use of space, equipment, material, personnel and increase capacities. Assist in developing plant layout in planning rearrangement of facilities, equipment and operations for better utilization of space and to increase capacities. Supports process validations by defining process to quality parameters, executing protocols, collecting/interpreting data and supporting protocol summary where needed. Monitors work for accuracy, neatness, and conformance to policies and procedures. Trains, motivates, monitors and evaluates performance of manufacturing employees. Develop and implement departmental cross training initiatives to allow for flexible resources and aid in improved capacities. Actively participates with internal and/or customer audits. Participates with activities directly related to ISO certification, and on-going conformance. Works closely with internal departments to assure commitment to customer is met in a timely manner. Performs other duties as assigned.

What we're looking for: Education: Bachelor’s degree preferred in a technical field, preferably life science, chemistry and/or engineering discipline, or equivalent experience. Experience: Minimum 5 years of progressive manufacturing experience and responsibilities in a lean environment, 1 of which must be in a supervisory capacity; or equivalent combination of education and experience. Life science, chemistry, chemical engineering or chemical production experience desired. Experience in cGMP manufacturing is a plus. Additional Qualifications: Familiarity with Chemical and/or Aseptic production processes and applications within similar industry preferred. Highly organized and self-motivated individual who can work independently with little supervision. Must have strong leadership skills and problem solving abilities. Excellent oral and written communication skills. Ability to perform risk assessment of products and processes and develop corrective measures. Must be able to manage multiple tasks and priorities and easily adapt to changing situations. Computer literacy applied to scheduling, procedure revisions and data management is required. Ability to take initiative, meet deadlines, and lead people in a team environment essential. Proven track record of reducing costs through process improvements and efficiencies. Must be hands‑on, team oriented and committed to business improvement processes.

Disclaimer: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.

Avantor is proud to be an equal opportunity employer. Why Avantor? Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science. The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor. We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world.

EEO Statement: We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law. If you need a reasonable accommodation for any part of the employment process, please contact us by email at [e-mail] and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address. For more information about equal employment opportunity protections, please view the Know Your Rights poster.