Production Supervisor - 3rd Shift

PL Developments Careers; Piedmont (SC); On-site; USD 55,000 - 85,000; Full time

Benefits offered by this job

Medical and Dental Benefits

401K with employer match

Paid Time Off and Paid Holidays

Tuition Assistance

Group Life Insurance

Job summary

PL Developments, also known as PLD, is seeking a Production Supervisor to oversee day-to-day pharmaceutical manufacturing operations at our Piedmont facility in South Carolina. The role ensures efficient production, quality adherence, and safety compliance, with some after-hours scheduling as project needs dictate.

The position is on-site, full-time, with a work schedule Sunday through Thursday 9:30pm–6:30am and potential overtime to meet deadlines.

Qualifications

• High School Diploma or equivalency required; associate or bachelor’s degree preferred.
• 5+ years of manufacturing experience; pharmaceutical experience preferred.
• At least three years of supervisory experience.
• Knowledge of FDA, OSHA, GMPs, GDPs preferred.
• Strong leadership, quality focus, and productivity drive.
• Ability to prioritize and perform under pressure.
• MS Office proficiency (Word, Excel).
• Excellent verbal and written communication; strong interpersonal skills.

Responsibilities

• Direct and coach supervisors and team leads to meet production goals.
• Plan material flow and communicate across levels to meet deadlines.
• Monitor performance indicators and production schedules.
• Ensure GMP, GDP, and safety compliance in production area.
• Coordinate with QA, mechanics, and engineers for process improvements.
• Train team on SOPs and manage inventory levels.
• Respond to safety incidents and implement corrective actions.
• Address deviations and root cause analyses with CAPAs.

Skills

Leadership

Communication

Problem-solving

Prioritization

Interpersonal skills

MS Office

Education

High School Diploma or equivalency

Associate or bachelor’s degree preferred

Tools

MS Office

Job description

513 Old Griffin Road
Piedmont, SC 29673, USA

• On-site
• Full-Time
• Requisition #: PRODU002672

Description

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

SUMMARY:

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.

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

JOB QUALIFICATIONS:

• High School Diploma or equivalency required, associate or bachelor’s degree preferred
• 5+ years of experience of working in a manufacturing environment (Pharmaceutical exp. 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 bark for quality and productivity
• Ability to effectively prioritize and execute tasks in a high-pressure environment
• Computer skills utilizing MS office, word, and Excel
• Must possess exceptional verbal and written communication skills
• Strong interpersonal skills and problem-solving skills

POSITION RESPONSIBILITIES:

• Provides support by directing and coaching, supervisors and team leads to achieve division of objectives and production goals
• Plan flow of materials through departments. Communicate properly and adequately to all personnel levels to ensure the production deadlines are met
• Monitors keep performance indicators
• Ensure that 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
• Responds quickly to all oral and written communication such accident reports, deviation reports. vacation and sick request, and absence reports
• Create and investigate operational deviations and determine root cause/CAPA’s with implementation strategiesPerforms other related duties as assigned by management

PHYSICAL REQUIREMENTS:

• Required to stand for long periods of time in 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: PLD is a proud equal opportunity employer offering many corporate benefits, including:

• 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

The EEO statement needs to be included in the detailed description... PL Developments is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

5 years: 5+ years of experience of working in a manufacturing environment (Pharmaceutical exp. preferred)

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor.