Production Supervisor

vwr; Paris (KY); On-site; USD 70,000 - 90,000; Full time

Job summary

Avantor is seeking a Production Supervisor (Drys) at our Paris, KY site to oversee daily manufacturing activities, plan and optimize production resources, and ensure quality and compliance with cGMP standards.

The role requires a technical Bachelor's degree (or equivalent) and at least five years in lean manufacturing, including supervisory experience. Strong leadership, attention to safety, and cross-functional coordination are essential for success.

Qualifications

• Bachelor's degree preferred in a technical field (life science, chemistry, or engineering) or equivalent experience.
• Minimum 5 years of progressive manufacturing experience in a lean environment, with at least 1 year in a supervisory role.
• Life science, chemistry, chemical engineering or chemical production experience desired.
• Experience in cGMP manufacturing is a plus.

Responsibilities

• Supervise and develop manufacturing employees to ensure safe, efficient operations.
• Plan, schedule, and coordinate departmental activities to meet sales orders and inventory requirements.
• Maintain and improve manufacturing procedures, batch records, SOPs and work instructions for quality and compliance.
• Conduct root-cause analysis and implement corrective actions to reduce non-conformities and costs.

Skills

Supervisory experience

Lean manufacturing

cGMP

Documentation

Education

Bachelor's degree preferred

Job description

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 preventive 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 live