EXPANSION Production Supervisor

Piramal Pharma Ltd; Lexington (KY); On-site; USD 65,000 - 85,000; Full time

Job summary

Piramal Pharma Solutions in Lexington, KY is seeking an Expansion Production Supervisor to oversee manufacturing operators across component preparation, filling, capping, sterilization and lyophilization, reporting to the Manufacturing Manager.

The role emphasizes adherence to cGMP, scheduling, and coordinating cross-functional operations to meet production goals, with a focus on leadership, training, and continuous improvement.

Qualifications

• 5+ years’ experience in a cGMP manufacturing environment.
• Experience with aseptic or lyophilization manufacturing is preferred.
• 2+ years’ experience leading teams, formal or informal.

Responsibilities

• Supervises Manufacturing Operators in proper operating techniques and procedures.
• Develops reports on scheduling, production goals, and equipment issues.
• Coordinates production schedules and cross-department communication.
• Develops employees through training, objectives, and policy communication.
• Ensures compliance with policies, cGMPs, safety, and housekeeping.
• Monitors schedules and ensures readiness objectives are met.
• Coordinates and controls production activities for optimal resources.
• Reviews projects for timely completion and evaluates performance.
• Ensures adequate resources (equipment, supplies, labor) are available.
• Performs SOP reviews and suggests process improvements.

Skills

Leadership

Communication

Analytical thinking

Problem solving

Team building

Documentation

Education

High School diploma or equivalent

Tools

Microsoft Office

Job description

Be the First to Apply

Division

Piramal Pharma Solutions

Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.

This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.

Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.

For more details, please visit : www.piramalpharmasolutions.com

Job Title

EXPANSION Production Supervisor

Job Description

Business: Pharma Solutions

Department: Operations (OPS)

Location: Lexington

Job Overview

Reporting to the Manufacturing Manager, the Manufacturing Supervisor oversees and coordinates the activities of Manufacturing Operators engaging in component preparation, filling, capping, autoclaving, terminal sterilization, compounding, and lyophilization production.

Reporting Structure

This position reports to the Manufacturing Manager.

Shift

Days

Key Responsibilities

• Supervises Manufacturing Operators in proper operating techniques and procedures
• Develops information and compiles reports concerning scheduling, production goals, equipment and maintenance problems and other studies or reports as requested
• Provides input in establishing production schedules
• Confers with other department management to coordinate the scheduling of operations to achieve required deadlines.
• Develops department employees through orientation, training, establishment of objectives, communication of rules and policies while building employee morale and motivation.
• Maintains compliance with company policies, cGMP’s, safety standards, and good housekeeping practices.
• Monitors production schedule and ensures readiness objectives are met.
• Supervises, coordinates, and controls the production and operating activities to ensure optimum utilization of personnel, materials, and equipment.
• Conducts continuous review and follow-up on projects to ensure completion of assigned work.
• Evaluates the performance and production of staff; maintains records on performance.
• Ensures adequate resources are available to manufacture product (equipment, supplies, and labor).
• Performs/ensures investigations and document corrections/modifications are done effectively and in a timely manner.
• Performs periodic review of all operation’s SOP’s and supplies management with feedback for process improvements.
• Performs production floor tasks as needed

Qualifications

• High School education or equivalent
• 5 + years’ experience in a cGMP manufacturing environment
• Experience working within aseptic or lyophilization manufacturing preferred
• 2+ years’ experience leading teams, either formally or informally
• Excellent written and verbal communication skills
• Excellent analytical and problem solving skills
• Excellent leadership and team building skills
• Technical writing experience, preferred
• Proficiency with Microsoft Office, preferred