EXPANSION Production Supervisor

Piramal Pharma Limited; Lexington (KY); On-site; USD 60,000 - 80,000; Full time

Job summary

Piramal Pharma Limited in Lexington is seeking an experienced Production Supervisor to oversee and coordinate the activities of Manufacturing Operators. This role involves ensuring compliance with safety standards and optimal utilization of resources.

The ideal candidate has over 5 years of experience in a cGMP manufacturing environment, strong leadership skills, and proficiency in Microsoft Office. The position offers a dynamic work environment with opportunities for team development.

Qualifications

• 5+ years’ experience in a cGMP manufacturing environment.
• Experience working within aseptic or lyophilization manufacturing preferred.
• 2+ years’ experience leading teams.

Responsibilities

• Supervises Manufacturing Operators in proper operating techniques.
• Develops reports concerning scheduling and production goals.
• Maintains compliance with company policies and safety standards.

Skills

Leadership

Communication

Analytical skills

Problem solving

Education

High School education or equivalent

Tools

Microsoft Office

Job description

## EXPANSION Production SupervisorApplylocations: Lexingtonposted on: Posted Todayjob requisition id: R00002518***Be the First to Apply*****Division**Piramal Pharma SolutionsPiramal 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.comJob TitleEXPANSION Production SupervisorJob DescriptionBusiness: Pharma Solutions Department: Operations (OPS) Location: Lexington**Job Overview** Reporting to theManufacturing 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