Staffing Resource Group, Inc is hiring: Manufacturing Supervisor in Marietta

Posted: 10/03/2025 Employment Type: Direct Hire Division: Life Sciences Job Number: JN -102025-20751 State: Georgia

Job Description

Manufacturing Supervisor

Title: Manufacturing Supervisor
Location: Marietta, GA
Industry: Pharmaceutical
Hours: M-F, 6am-2:30pm with mandatory 2nd shift hours ranging from (M-F, 2pm-10:30pm) and rotating weekends
Salary: Competitive within industry
Employment Type: Direct hire

Position Overview:
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.

Environment:
Client is a fully integrated biopharmaceutical company focused on developing, manufacturing and commercializing specialty products.

Duties and Responsibilities:

• Monitors and supervises the daily operations of the Manufacturing and Packaging production department, ensuring compliance to cGMPs, 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 SOPs.
• Follow and enforce company guidelines set forth in the employee 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, SOPs, 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.

Qualifications

• 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 required (within pharmaceuticals)
• Must have Pharmaceutical experience within OSD (oral solid dosage)
• Must have hands-on experience with blending, coating, compression, tablet press machines
• 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 lift 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.

EOE/ADA