Production Supervisor, 2nd Shift

Osmotica Holdings Corp; Marietta (GA); On-site; USD 70,000 - 85,000; Full time

Job summary

A leading company in the pharmaceutical industry is seeking a Manufacturing Supervisor in Marietta, Georgia. The successful candidate will oversee production operations, ensuring compliance with cGMP standards while leading and developing staff. This role requires strong mechanical and mathematical skillsets, as well as a commitment to regulatory standards, making it a key position in maintaining the quality of production processes.

Qualifications

• Preferred BS in Science or relevant work experience in Manufacturing/pharmaceutical.
• Supervisory experience preferred.
• Knowledge of cGMP and compliance issues required.

Responsibilities

• Leads Production Technician staff with daily activities and training.
• Monitors daily operations ensuring compliance with safety procedures.
• Develops and revises documentation to maintain regulatory compliance.

Skills

Mechanical aptitude

Mathematical aptitude

Communication

Training

Education

BS in Science or related field

Tools

Microsoft Windows

Microsoft Word

Microsoft Excel

Microsoft Power Point

Job description

MANUFACTURING SUPERVISOR

Main Duties and Responsibilities

The Production Supervisor is responsible for leading Production Technician staff with daily activities and training. Provide verbal and written instructions in a clear and concise manner.

Job Responsibilities

• Monitors and supervises the daily operations of the Manufacturing and Packaging production department, ensuring compliance to cGMP’s, written and safety procedures at all times.
• Reviews documentation generated by the Manufacturing and Packaging production department (i.e., batch records, log books, forms, etc.) for completeness and correctness; Executes production schedule.
• Develops and/or revises documentation (i.e., batch records, forms, standard operating procedures, etc.) to maintain compliance with regulatory requirements.
• Troubleshoots production problems, document findings, and implement solutions while providing all information to Management for risk assessment; schedule preventative maintenance activities.
• Trains and evaluates new employees as required.
• Conduct performance appraisals as required.
• Communicate with the incoming/outgoing supervisor and shift personnel to assure continuity and complete information pass-off.
• Develop employees and maintain proper documentation to ensure employee competence.
• Follow and enforce company SOP’s.
• Follow and enforce company guidelines set forth in the Osmotica handbook.
• Assure production employees attend annual cGMP training.
• Perform transactions using electronic inventory system related to manufacturing activities.
• Write and revise standard operating procedures, as required.
• Proven knowledge of company-supported application software (i.e., Microsoft Windows, Word, Excel and Power Point.
• Point out possible difficulties and assure compliance with the production schedule.
• Assure and provide classroom and hands-on training for batch records, SOP’s, and cGMP training for manufacturing.
• Assure that all batch records are reviewed, corrected, and submitted to QA within 48 hours of batch completion.
• Keep current with FDA/cGMP, OSHA, EPA regulations as they relate to the department. Initiate training or proper action as required.
• Review attendance records and take disciplinary action as required.

Requirements

• BS in Science or related field preferred. Relevant work experience in Manufacturing and/or pharmaceutical industry may be considered in lieu of degree
• Previous supervisory experience is preferred.
• Strong mechanical and mathematical aptitude

Core Competencies

• Ability to work 1st, 2nd and 3rd shifts and overtime as required.
• Ability to work weekends and holidays as required.
• Ability to wear respirators, PAPR and other protective equipment
• Ability to perform physical activity (ability to life 40 lbs without assistance)
• Demonstrate the ability to write legibly and communicate clearly by successful completion of a writing sample
• Experience and knowledge of cGMP and compliance issue.