EXPANSION Production Supervisor

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Division

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.

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Job Title

Job Description

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 cGMPs 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 operations SOPs 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