Production Supervisor - 3rd Shift

PL Developments, also known as PLD, is a leading manufacturer, packager, and distributor of over-the-counter (OTC) pharmaceutical products and consumer healthcare goods.

About the role

The Production Supervisor will supervise the day-to-day operations of a pharmaceutical manufacturing facility, ensuring efficient production processes, adherence to quality standards, and compliance with safety regulations. This role involves optimizing resources and collaborating with various departments to achieve operational goals. The role may require work outside scheduled hours to accommodate project deadlines and operational needs.

Schedule

Sunday - Thursday, 9:30pm-6:30am (additional hours as needed)

Responsibilities

• Provides support by directing and coaching supervisors and team leads to achieve division objectives and production goals
• Plan flow of materials through departments
• Communicate properly and adequately to all personnel levels to ensure production deadlines are met
• Monitors key performance indicators
• Ensure the production area adheres to schedules and carries out all necessary activities to ensure the timely availability of products for the production floor
• Monitor and control production processes to achieve optimal output and minimize downtime
• Ensure the efficient use of resources, including materials and labor
• Identify opportunities for process improvement and cost reduction by partnering with Quality Assurance, Mechanics, and Industrial Engineers
• Implement and enforce production schedules and quality standards
• Provide instruction or coordinate training for team members on all relevant, updated Standard Operating Procedures (SOPs)
• Monitor and manage inventory levels to prevent shortages or overstock situations
• Coordinate with supply chain and logistics teams to optimize material availability
• Uphold safety protocols and regulations, promoting a safe working environment for all team members
• Investigate and report safety incidents to EHS Specialist and Operations Management; implement corrective actions
• Maintain and enforce quality control/quality assurance procedures to ensure products meet required specifications
• Respond quickly to all oral and written communications such as accident reports, deviation reports, vacation and sick requests, and absence reports
• Create and investigate operational deviations and determine root cause/CAPAs with implementation strategies
• Perform other related duties as assigned by management

Requirements

• High School Diploma or equivalency required; associate or bachelor’s degree preferred
• 5+ years of experience working in a manufacturing environment (pharmaceutical experience preferred)
• At least three years of experience as a supervisor
• Working knowledge of FDA and OSHA regulations, Good Manufacturing Practices (GMPs), and Good Documentation Practices (GDPs) preferred
• Proven ability to effectively lead while constantly raising the bar for quality and productivity
• Ability to effectively prioritize and execute tasks in a high-pressure environment
• Computer skills utilizing MS Office, Word, and Excel
• Exceptional verbal and written communication skills
• Strong interpersonal and problem-solving skills
• Bilingual in Spanish preferred

Physical Requirements

• Required to stand for long periods of time in a production environment and/or working at a desk on a computer for long periods of time
• Capable of frequently lifting and carrying items weighing 25–45 lbs. in a production environment
• Some exposure to hazardous chemicals and other active chemical raw materials or ingredients is possible
• Must be able to wear proper gowning and PPE in production areas, as required, to meet GMP and/or OSHA requirements

Benefits

• Medical and Dental Benefits
• Vision
• 401K with employer match
• Group Life Insurance
• Flex Spending Accounts
• Paid Time Off and Paid Holidays
• Tuition Assistance
• Corporate Discount Program
• Opportunities to flourish within the company