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Piramal Pharma Solutions

Production Supervisor

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What they do

A Production Supervisor supervises workers and production schedules, monitors supplies, and oversees quality assurance at a production facility.

$66,397 / year median in Kentucky

+5% projected growth

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Job Description

Company Overview Piramal Pharma Solutions (PPS) is a dynamic Contract Development and Manufacturing Organization (CDMO) dedicated to delivering comprehensive drug development and manufacturing solutions across the entire pharmaceutical lifecycle. Our globally integrated network of facilities enables us to serve a diverse range of clients with innovative services, including biologics, sterile fill/finish, potent APIs, and advanced manufacturing technologies. Job Overview We are seeking an energetic and detail-oriented Production Supervisor to lead our manufacturing operations. In this pivotal role, you will oversee daily production activities, ensure adherence to quality standards, and drive continuous improvement initiatives. Your leadership will be instrumental in maintaining efficient workflows, optimizing production schedules, and fostering a culture of safety and excellence within our manufacturing plant. 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
Pay:
Up to $95,000.00 per year
Benefits:
401(k) 401(k) matching Dental insurance Employee assistance program Flexible spending account Health insurance Health savings account Life insurance Paid time off Referral program Relocation assistance Retirement plan Tuition reimbursement Vision insurance
Work Location:
In person