Supervisor, Manufacturing Operations - 3rd Shift

Amneal Pharmaceuticals

Piscataway Township (NJ)

On-site

USD 70,000 - 90,000

Full time

14 days+

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Job summary

A leading pharmaceutical company is seeking a Supervisor for Manufacturing Operations on the 3rd shift. The role involves managing daily production activities, ensuring compliance with safety and quality standards, and optimizing production efficiency. Candidates should have significant experience in manufacturing and supervisory roles, along with relevant technical expertise. This is a full-time position that offers an opportunity to lead a dedicated team in a dynamic environment.

Qualifications

  • 5 years in manufacturing with supervisory experience.
  • Technical expertise in Solid Dosage formulations and FDA regulations.

Responsibilities

  • Supervise and train production staff to achieve high performance.
  • Conduct inspections to ensure compliance with safety regulations.
  • Monitor production tooling and troubleshoot issues.

Skills

English Communication
Basic Math Skills
Mechanical Skills
Forklift Operation

Education

High School or GED
Bachelor's Degree in Manufacturing Engineering

Tools

Six Sigma
Lean Principles

Job description

Supervisor, Manufacturing Operations - 3rd Shift

Join to apply for the Supervisor, Manufacturing Operations - 3rd Shift role at Amneal Pharmaceuticals.

Job Description

The Supervisor of Manufacturing Operations will manage and oversee daily production activities to ensure adherence to cGMPs and SOPs, optimize production efficiency, and improve quality while minimizing raw material waste. Responsibilities include supervising production schedules, leading a team of operators and technicians, ensuring smooth operations, and maintaining high safety and quality standards.

Essential Functions
  • Supervise, train, and motivate production staff to achieve high performance and productivity; manage training and development to ensure compliance with cGMPs and enhance work quality and quantity.
  • Conduct regular inspections of facilities and equipment to ensure compliance with SOPs, cGMPs, and safety regulations; coordinate maintenance and repairs; collaborate with Engineering on equipment upgrades.
  • Ensure raw material usage and product yields meet or exceed standards.
  • Work with the department manager to assess needs, plan, schedule, and prioritize tasks to improve customer service and departmental efficiency.
  • Provide technical support on equipment and processes; troubleshoot issues; monitor and adjust production tooling; evaluate tooling effectiveness.
  • Monitor safety protocols and address unsafe conditions promptly.
Qualifications

Education:

  • High School or GED required.
  • Bachelor's Degree in Manufacturing Engineering, Industrial Engineering, or related field preferred.

Experience:

  • At least 5 years in manufacturing, including supervisory experience in Softgel, Pharmaceutical, or Manufacturing sectors.

Skills:

  • Proficient in English communication; able to understand and follow procedures; basic math and mechanical skills; forklift operation (preferred).

Knowledge:

  • Technical expertise in Solid Dosage formulations, OROS technology, Laser Drilling, Ink Printing, and knowledge of FDA & DEA regulations.
  • Familiarity with Six Sigma and Lean principles; coordination with Engineering for maintenance and validation; experience with CAPA, change control, and SOP updates; knowledge of Liquid Filled Hard Gelatin Capsule manufacturing and machinery support for extended-release formulations.
Additional Details

Seniority Level: Not Applicable

Employment Type: Full-time

Job Function: Manufacturing, Production, Engineering

Industry: Pharmaceutical Manufacturing

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