Production Supervisor

Production Supervisor
Title: Production Supervisor
Location: Marietta, GA
Industry: Pharmaceutical Manufacturing
Hours: M-F, 2nd shift, 2pm-10:30pm with OT and rotating weekends
Salary: Competitive compensation package (eligibility for company bonus, 401k, health, dental and vision) and relocation assistance provided for the right candidate
Employment Type: Direct hire

Company Overview:
We're partnering with a fully integrated US based biopharmaceutical organization focused on advancing specialty treatments. With a growing and diverse product pipeline, including complex generics and specialty formulations, this is an opportunity to step into a leadership role where your work directly supports life-changing therapies. If you're a hands-on leader with strong pharmaceutical manufacturing experience, this role offers the chance to drive production excellence, mentor teams, and grow your leadership career in a highly regulated, high-impact environment.

Position Overview:
As a Production Supervisor, you'll lead a team of Production Technicians and oversee daily manufacturing and packaging operations. You'll play a key role in ensuring efficiency, compliance, and continuous improvement.

Duties and Responsibilities:

• Monitors and supervise the daily operations of the Manufacturing and Packaging production department, ensuring compliance with cGMP's always written and safety procedures.
• Reviews documentation generated by the Manufacturing and Packaging production department (i.e., batch records, logbooks, 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.
• Troubleshoot production problems, document findings, and implement solutions while providing all information to Management for risk assessment; schedule preventative maintenance activities.
• Train, mentor and develop team members to build a high-performing workforce.
• Conduct performance evaluations and support employee development plans.
• 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.
• Support SOP creation, revisions, and compliance initiatives.
• 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.
• Proven knowledge of company-supported application software (i.e., Microsoft Windows, Word, Excel and Power Point.
• Point out possible difficulties and ensure 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.

Qualifications

• Bachelor's degree in a scientific field (or equivalent experience).
• 3+ years of supervisory experience in pharmaceutical manufacturing
• Strong experience in oral solid dosage (OSD) environments
• Hands on experience with blending, compression, coating and tablet press equipment
• Solid understanding of cGMP and regulatory compliance
• Strong problem-solving, mechanical and analytical skills
• Effective communication and leadership abilities

Work Environment and Requirements

• Ability to work flexible shifts (1st, 2nd, 3rd), weekends, holidays and overtime as needed
• Ability to wear respirators, PAPR and other protective equipment
• Ability to perform physical activity (ability to lift 40lbs without assistance)
• Demonstrate the ability to write legibly and communicate clearly by successful completion of a writing sample
• Comfortable working in a regulated manufacturing environment

SRG4 Life Sciences delivers flexible staffing solutions nationwide, specializing in pharmaceutical, CDMO/CMO, medical device, clinical research, PBM, pharmacy, food and beverage, nutraceutical, laboratory, and consumer product sectors. We provide contract, contract-to-hire, and direct hire placements across a wide range of critical roles including Scientists, Formulators, Engineers, QA/Regulatory Affairs, Microbiologists, Manufacturing Technicians, Supply Chain/Procurement Specialists, Project Managers, and Business Development professionals. SRG4 Life Sciences operates on a relationship-driven model-partnering closely with clients to understand not only the role, but the company's culture, goals, and vision. Our mission is to match purpose-driven professionals with organizations committed to advancing human health, building long-term partnerships that drive innovation, quality, and performance.

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