Company

Pl DevelopmentsSee more

addressAddressPiedmont, SC
type Form of workFull-Time
CategoryManufacturing

Job description

Job Description

Work Schedule: Friday, Saturday, Sunday 6a - 6:30p

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)
  • 3+ years working in a lead role
  • Working knowledge of FDA and OSHA regulations, Good Manufacturing Practices (GMPs) and Good Documentation Practices (GDPs) preferred
  • Must possess exceptional verbal and written communication skills
  • Strong problem-solving skills
  • Proficient in MS Office (Word and Excel)
  • Ability to clearly communicate shift goals and manage operational activities for successful attainment

POSITION RESPONSIBILITIES:

  • Supervise and lead a team of production workers and Compounders by providing guidance, support, and motivation.
  • Schedule and assign tasks to ensure smooth workflow and meet production goals.
  • Supervise the production line to provide directions to line leaders to meet the shift's production goals.
  • Ensure that the compounding 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.
  • Address and resolve quality issues promptly.
  • Create and investigate operational deviations and determine root cause/CAPA’s with implementation strategies.
  • All other duties as assigned

PHYSICAL REQUIREMENTS:

  • Position exposed to various work environments such as office, production areas, warehouse, etc.
  • 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.
  • May occasionally lift up to 50 lbs.
  • Some exposure to hazardous chemicals and other active chemical raw materials or ingredients is possible.
  • Weekend or extended work week hours may be required based on production schedule
  • Must be able to wear proper gowning and PPE in production areas, as required, to meet GMP and/or OSHA requirements.

#HP1

Company Description
PL Developments is an over-the-counter pharmaceutical manufacturing and packaging company, headquartered in New York. We have an excellent work environment, truly invest in our people, and believe in great work/life balance. We offer a comprehensive benefits package.
PLD participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Refer code: 8612737. Pl Developments - The previous day - 2024-03-17 18:17

Pl Developments

Piedmont, SC
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