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Pharmaceutical Manufacturing Solid Dosage Supervisor

The Staffing Resource Group, Inc

Marietta, GA

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JOB DETAILS
SKILLS
Analysis Skills, Biology, Biotech and Pharmaceutical, Business Development, Clinical Research, Communication Skills, Consulting, Continuous Improvement, Current Good Manufacturing Practice (cGMP), Disciplinary Action, Documentation, Documentation Review, Drug Manufacturing, Environmental Impact, Environmental Protection Agency (EPA), FDA (Food and Drug Administration), Food and Beverage Industry, Human Health, Identify Issues, Inventory Transactions, Leadership, Lift/Move 40 Pounds, Maintain Compliance, Manufacturing, Manufacturing Management, Manufacturing Operations, Manufacturing Systems, Medical Equipment, Mentoring, Microsoft Excel, Microsoft PowerPoint, Microsoft Windows Operating System, Microsoft Word, OSHA, Operations, Operations Management, People Management, Performance Analysis, Performance Reviews, Pharmacy, Preventative Maintenance, Problem Solving Skills, Production Control, Production Management, Production Schedule, Project/Program Management, Purchasing/Procurement, Quality Assurance, Regulations, Regulatory Compliance, Regulatory Requirements, Risk Analysis, Safety Process, Software Administration, Staff Development, Standard Operating Procedures (SOP), Supply Chain, Team Lead/Manager, Writing Skills
LOCATION
Marietta, GA
POSTED
30 days ago
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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About the Company

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The Staffing Resource Group, Inc

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