Production Supervisor

Job DescriptionProduction SupervisorTitle: Production SupervisorLocation: Marietta, GAIndustry: Pharmaceutical ManufacturingHours: M-F, 2nd shift, 2pm-10:30pm with OT and rotating weekendsSalary: Competitive compensation package (eligibility for company bonus, 401k, health, dental and vision) and relocation assistance provided for the right candidateEmployment Type: Direct hireCompany 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 manufacturingStrong experience in oral solid dosage (OSD) environmentsHands on experience with blending, compression, coating and tablet press equipmentSolid understanding of cGMP and regulatory complianceStrong problem-solving, mechanical and analytical skillsEffective communication and leadership abilities Work Environment and RequirementsAbility to work flexible shifts (1st, 2nd, 3rd), weekends, holidays and overtime as neededAbility to wear respirators, PAPR and other protective equipmentAbility 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 sampleComfortable working in a regulated manufacturing environmentSRG4 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.EOE/ADA