Supervisor, Production Operations - Second Shift

Kindeva Drug Delivery; Lexington (KY); On-site; USD 75,000 - 110,000; Full time

Job summary

Kindeva Drug Delivery is seeking a 2nd Shift Supervisor, Manufacturing in Lexington to lead on-the-floor execution for commercial and development campaigns, ensuring safe, compliant, and efficient operations.

The role emphasizes developing manufacturing technicians, coordinating resources, and driving KPI performance while maintaining strong cGMP adherence and regulatory readiness.

Qualifications

• Demonstrated leadership in a manufacturing setting with cGMP experience.
• Strong communication and interpersonal skills for cross-functional collaboration.
• Proven ability to drive KPIs and continuous improvement.
• Experience with staffing, training, and developing manufacturing technicians.
• Knowledge of FDA/cGMP requirements and quality systems.

Responsibilities

• Plan and manage commercial and development manufacturing campaigns.
• Lead, mentor, and develop a team of manufacturing technicians.
• Meet or exceed KPI targets for productivity, quality, and safety.
• Provide on-the-floor leadership for 50%+ of the shift.
• Ensure compliance with cGMP and regulatory requirements.

Skills

Leadership

Communication

Problem-solving

Change management

Team development

Education

High school diploma

Bachelor's degree in science/technical

Tools

ERP

MES

SCADA

OSI PI

Job description

Our Work Matters At Kindeva, we make products that improve people's lives. Every day, our teams help develop and manufacture pharmaceutical therapies and medical devices that patients around the world depend on.

Our Work Matters At Kindeva, we make products that improve people's lives. Every day, our teams help develop and manufacture pharmaceutical therapies and medical devices that patients around the world depend on.

Why Kindeva?

• Purpose-driven work environment
• Significant growth potential
• Collaborative team culture
• Direct impact on patient care
• Industry-leading innovation

At Kindeva, we're more than a global Contract Development and Manufacturing Organization (CDMO). We're a team dedicated to improving patient outcomes through innovation, collaboration, and operational excellence.

We're looking for a 2nd Shift Supervisor, Manufacturing to provide hands-on leadership for commercial and development manufacturing operations at our Lexington site.

The Impact You Will Make

As a 2nd Shift Supervisor, Manufacturing, you will lead on-the-floor shift execution for commercial and development manufacturing campaigns, ensuring operations are performed safely, effectively, and in accordance with current Good Manufacturing Practices (cGMP) standards and regulatory requirements.

You will be responsible for developing and leading manufacturing technicians, coordinating resources to meet production requirements, driving department Key Performance Indicators (KPIs), and leading change and continuous improvement initiatives.

This is a highly visible, floor-focused leadership role, with greater than 50% of the workday spent providing direct leadership within the manufacturing operation.

The successful candidate will exemplify Kindeva's KIND Values: Kinetic, Innovation, Now, and Delivery.

Responsibilities

Leadership & Manufacturing Operations

• Plan and manage commercial and development manufacturing campaigns, coordinating with cross-functional teams to ensure timely and successful execution of production processes.
• Manage resource allocation, including personnel, equipment, and materials, to meet production schedules and goals.
• Lead, mentor, and develop a team of manufacturing technicians, fostering a culture of continuous improvement and high performance.
• Lead shift execution to meet or exceed performance KPI targets, including productivity, quality, and safety metrics.
• Provide visible and vocal leadership on the manufacturing floor for greater than 50% of the daily work period.

Compliance & Quality Assurance

• Ensure manufacturing processes and outputs meet the strict quality standards required for pharmaceutical products and medical devices.
• Maintain compliance with cGMP, United States Food and Drug Administration (FDA), and other relevant regulatory requirements by enforcing proper documentation, procedures, and audit readiness.
• Conduct regular facility assessments and participate in internal and external audits, addressing findings promptly.

Change Management & Continuous Improvement

• Lead and manage change initiatives within the department, including process improvements, system upgrades, and organizational changes.
• Communicate effectively with stakeholders at all levels to ensure effective shift-to-shift transitions that minimize disruption to operations.
• Monitor and assess the impact of changes on manufacturing performance.

Qualifications

Required

• High school diploma.
• 3+ years of supervisory experience in cGMP pharmaceutical manufacturing.
• Proven leadership experience, including staff management, training, and development.
• Strong understanding of cGMP regulations, FDA requirements, and other relevant industry standards.
• Demonstrated success in driving staff performance through KPIs and continuous improvement initiatives.
• Strong problem-solving, decision-making, and change management skills.
• Excellent communication and interpersonal skills.

Preferred

• Bachelor’s degree in a science or technical discipline.
• Experience with medical device manufacturing.
• Certification in Lean Six Sigma or related continuous improvement methodologies.
• Proficiency with manufacturing software and systems, including Enterprise Resource Planning (ERP), Manufacturing Execution Systems (MES), Supervisory Control and Data Acquisition (SCADA), and OSI PI.

Physical Requirements

• Ability to regularly use hands to handle materials and supplies.
• Ability to use computers for extended periods each day.
• Ability to communicate effectively through telephone and electronic communication methods.
• Ability to regularly stand and walk for extended periods.
• Ability to occasionally lift and/or move up to 25 pounds.

#WH

California residents should review our Notice for California Employees and Applicants before applying.

Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees—regardless of format—without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.

Equal Opportunity Employer

Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.