Production Supervisor
Posted: 02/20/2026
Employment Type:
Direct Hire
Division: Life Sciences
Job Number: JN -022026-20954
State: Georgia
Job Description
Production Supervisor
Title: Production Supervisor
Location: Marietta, GA
Industry: Pharmaceutical
Hours: M-F, 2pm-10:30pm with OT 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. Our diversified product portfolio in the specialty neurology and women's health space, together with our non-promoted complex formulations of generic drugs, form the foundation of our unwavering commitment to improve patients' lives.
Duties and Responsibilities:
EOE/ADA
Title: Production Supervisor
Location: Marietta, GA
Industry: Pharmaceutical
Hours: M-F, 2pm-10:30pm with OT 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. Our diversified product portfolio in the specialty neurology and women's health space, together with our non-promoted complex formulations of generic drugs, form the foundation of our unwavering commitment to improve patients' lives.
Duties and 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 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, 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.
- BS in Science or related field preferred. Relevant work experience in Manufacturing and/or pharmaceutical industry may be considered in lieu of degree
- Minimum three years supervisory experience required (within pharmaceuticals in similar role)
- 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
- 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.
EOE/ADA
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Discover exciting job opportunities in the vibrant area around Marietta, Georgia! This charming city offers a perfect blend of Southern hospitality and modern innovation, making it an ideal place to grow your career. With easy access to fantastic amenities like the beautiful Marietta Square, home to galleries, theaters, and delicious southern cuisine, as well as nearby attractions such as Kennesaw Mountain National Battlefield Park and rousing games at the Truist Park, home of the Atlanta Braves, Marietta promises a dynamic and fulfilling lifestyle. Explore our job listings today and unlock your potential in this captivating region!
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