Endo

Supvervisor, Production

Endo  •  United States (Onsite)  •  9 days ago
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Job Description

Why Us?

At Par Health, we believe great healthcare is built on getting the essentials right. We’re looking for passionate, talented individuals who share our commitment to improving lives. With 4,000+ team members worldwide, we lead with pride and purpose—prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn’t just our tagline, it’s the higher standard we live by every day.

Ensure all work rules, safety rules and policies of the St. Louis Plant are followed. Supervise employees on a daily basis, provide mentoring, coaching, and discipline as needed. Schedule manpower to support department timelines and production goals. Submit maintenance work orders and issue permits as needed to maintain the equipment of the building.

JOB DUTIES

  • Ensure the operation of department/building are operated and maintained safely, efficiently and effectively.
  • Manage work team and staff including collective bargaining unit. Facilitate objectives by providing clear and continuous direction to staff. Develop, coach and mentor subordinates for existing and/or future roles.
  • Responsible for ensuring all direct reports are properly trained in areas directly related to their job responsibilities as well as company policies, quality policies, and safety/environmental policies.
  • Lead, coach and train employees toward team concepts and foster an environment for empowered, high-performance environment.
  • Schedule efficient daily manpower requirements based on plant requirements.
  • Responsible for monitoring the weekly schedules through interface with Customer Service, Planning, and Logistics, to ensure timely customer service.
  • Ensure specified product quantity levels, including raw materials and product specifications are available.
  • Motivate associates to ensure that predetermined productivity, cost, and quality standards are achieved or exceeded.
  • Responsible for handling grievances, exceptions, and incident reports.
  • Ensure direct reports comply with all company and/or regulatory policies for FDA, EPA, DEA, OSHA, and all other applicable regulations as well as procedures related to the areas of cGMP, SOPs, DOT, etc.
  • Participate in budget preparation while tracking and establishing progress towards organizational goals.
  • Interacting with a wide range of individuals at all levels. Ensuring accurate communication of operating status, financial and operational metrics at all established intervals.
  • Ensure contract compliance with collective bargaining agreements.
  • Responsible for special projects assigned to include but not limited to Lean Manufacturing initiatives, six sigma projects, safety initiatives, etc.
  • Drive cost savings through improvements and lean implementation.
  • Lead and/or support all investigations, manufacturing exceptions, product failures, RCA and customer complaints at the appropriate level with complete and comprehensive detail.
  • Responsible for establishing and maintaining detailed records.
  • Design and implement work methods and procedures to increase productivity and improve service within an assigned department.

DEPARTMENT SPECIFIC FUNCTIONS

Other duties as assigned with or without accommodation.

REQUIREMENTS

Education:

Bachelor’s degree required or an equivalent combination of experience, education and competencies. Preferred area of emphasis degree in Chemical Engineering, Chemistry or a related field is highly preferred. Equivalent work experience is typically six years of related, progressive work experience would be needed for candidates applying for this position who do not possess a bachelor's degree.

Minimum of three years manufacturing experience and two years supervisory experience is required.

Strong working knowledge of OSHA and FDA Regulations required.

Experience:

Experience with a wide variety of unit operations such as distillation, filtration, centrifugation, drying, etc.

Experience with hazardous chemicals and flammables. Familiarity with PSM is preferred.

Experience within union environments is a plus.

Experience in a chemical or related industry preferred.

Candidate must have a demonstrated record of successful accomplishments in managing people, excellent interpersonal communication skills, and the ability to handle multi-tasks simultaneously in a fast-paced cGMP work environment.

Preferred Skills/Competencies:

Knowledge of chemical manufacturing and plant support systems

Understanding and working knowledge of cGMPs.

Good problem solving skills and attention to detail.

Ability to analyze, prioritize and manage multiple tasks.

Mechanical knowledge of production equipment.

Knowledge of Lean Manufacturing and Six Sigma Tools is a plus

Must be willing to work a variety of shifts if required.

Other Skills/Certifications:

Proficiency in Microsoft Office Products (Word, Excel, Outlook), good planning and organizing skills, good written and oral communication skills, ability to keep detailed records.

WORKING CONDITIONS:

This is a managerial position supervising others in a manufacturing environment. Working hours are a rotating shift schedule requiring night and weekend work. Production areas may not be climate controlled.

MACHINES, TOOLS, EQUIPMENT AND WORK AIDS:

The following list may be representative but not all inclusive of those commonly associated with this position:

Computer, projector, printer, various software, calculator, and general office equipment (e.g. copier, fax, etc.).

EEO Statement:

We comply with all applicable federal, state, and local laws prohibiting discrimination and harassment, and provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or genetic information, or any other classification protected by federal, state or local law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. 

Endo

About Endo

Endo combined with Mallinckrodt Pharmaceuticals in 2025 to better serve customers and improve outcomes for the patients we support.

From this union, we established two focused, standalone companies:

– Keenova Therapeutics, a branded therapeutics business

– Par Health, a generics and sterile injectables business

To learn more, follow Keenova and Par Health on LinkedIn and visit keenova.com and parhealth.com.

Industry
Chemicals & Materials
Company Size
1,001-5,000 employees
Headquarters
Malvern
Year Founded
Unknown
Website
endo.com
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