Production Supervisor

Paladin Labs Inc.

Greenville (IL)

On-site

USD 70,000 - 95,000

Full time

3 days ago
Be an early applicant

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

Par Health in Greenville, IL is seeking a Production Supervisor to oversee day-to-day production, planning, testing, and implementation of methods, processes and operations for new and existing products. You will ensure effective use of materials, equipment and personnel while minimizing costs and maintaining records.

You will lead and develop staff, ensure training and qualification, and drive continuous improvement using Six Sigma and Lean principles.

Qualifications

  • Proficient with standard MS Office apps and data entry.
  • Familiarity with database software and reporting tools.
  • Experience in pharmaceutical manufacturing is a plus.

Responsibilities

  • Oversee day-to-day production, planning, testing, and implementation of plant processes.
  • Ensure effective use of materials, equipment and personnel to produce quality products at minimized cost.
  • Develop systems to maintain reports and records of products and performance.
  • Select, develop, and coach staff to ensure efficient operation and training compliance.
  • Drive continuous improvement using Six Sigma and Lean principles.
  • Maintain safety, quality, and regulatory compliance across shifts.

Skills

MS Office
Database software

Education

Four-year degree
Equivalent experience

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 a global workforce, 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.

Job Description Summary

The Production Supervisor at the Greenville, IL Plant will oversee the day-to-day-production, planning, testing, and implementation of Company methods, processes/policies and operations for new and existing products. Ensure the effective use of materials, equipment and personnel in producing quality products while minimizing costs. Develops systems to maintain reports and keep records of company products. Select, develop, and evaluate personnel to ensure the efficient operation of the area of responsibility. Ensure all employees are properly trained and qualified to perform their assignments. Partner with teams to focus on continuous improvement utilizing Six Sigma and Lean principles.

Job Description ESSENTIAL FUNCTIONS:
  • Engage and direct employees to ensure departmental/plant goals and objectives are met.
  • Determine priorities, set up schedules, assign employees to scheduled jobs, and ensure compliance with SOP’s, cGMPs, company policies, work rules, and safety procedures.
  • Responsible for work outputs of area employees.
  • Utilizes shop floor metrics/visual factory to engage employees.
  • Ensure availability of materials, equipment, and paperwork.
  • Strong knowledge of Good Document Practices to review/audit required documents and ensure accurate completion of all paperwork.
  • Improve the overall department efficiency and processes by implementing improvement projects.
  • Deliver training to new and current employees as required and update training records.
  • Monitor attendance and performance of subordinates.
  • Coach and counsel employees through two-way engagement.
  • Take Corrective action when appropriate.
  • Investigate abnormalities and implement corrective and preventive actions for these abnormalities.
  • Report to functional leader on departmental issues, activities, and accomplishments.
  • Attend, participate, and conduct meetings as required. Including cross-functional meetings when needed.
  • Perform safety audits.
  • Drive safety/quality improvement ideas and performance.
  • Participate on Safety/Quality Teams.
  • Assists in the prevention of accidents and injuries by conducting regularly scheduled safety meetings.
  • Conducts Root Cause Investigations for all injuries and incidents, ensuring consistent discipline and retraining.
  • Create incident, accident, and counseling reports.
  • Establish and maintain a clean, safe work environment in compliance with Company/Occupational Safety and Health Administration (OSHA) standards.
  • Ensure that resolving employee conflicts remains a priority; ensure that disputes and safety/performance issues are addressed and that the appropriate documentation is retained for the employees’ personnel file.
  • Ensure that all employees comply with physicals, drug or alcohol testing and training required by regulatory agencies.
  • Troubleshoot problems with equipment and enter work requests for Maintenance when applicable.
  • Issue all permits needed to ensure work can be done safely (pipe breaking, confined space, lock/tag out, hot work, tank entry, etc.).
  • Partner with functional leaders to drive improvement in production quality and yields.
  • Manage the Collective Bargaining Agreement (CBA) in a consistent manner.
  • Must be willing to take on rotational assignments for development/growth opportunities.
  • Perform other tasks as directed by management.
  • Work rotating shifts.
MINIMUM REQUIREMENTS:
  • Education: Four-year degree (business, technical) preferred and/or equivalent experience required.
  • Experience: Minimum of three to five years' experience in the pharmaceutical industry with a minimum of two years supervisory experience.
  • Lean/Six Sigma certification experience preferred.
Preferred Skills/Qualifications:
  • Perform the functions of arithmetic: add, subtract, multiply and divide all units of measure; compute ratio, rate and percent; calculate variables and formulas.
  • Ability to apply logical thinking to define problems, collect data, establish facts and draw valid conclusions, to interpret an extensive variety of technical instructions in mathematical or diagrammatic form and to deal with abstract and concrete variables.
  • Knowledge of pharmaceutical manufacturing and plant support systems.
  • Experience and training in Six Sigma, Lean Manufacturing or similar programs.
  • Experience in driving efficiency improvements and cost savings in a manufacturing or similar environment.
  • Willingness to obtain required bachelor's degree.
Skills/Competencies:
  • Intermediate to advanced computer skills including Microsoft Office Suite and various database software.
  • Attention to detail and good organizational skills.
  • Strong interpersonal, communication, and writing skills.
  • Basic supervisory skills.
  • Demonstrate initiative and ability to perform as part of a team.
  • Knowledge of pharmaceutical processes and equipment.
Other:

The expected salary for this role is $70,000 to $95,000 commensurate with experience.

ORGANIZATIONAL RELATIONSHIPS/SCOPE:

This position reports to the Production Superintendent. Incumbent works independently and provides a high level of initiative and creativity to general duties. Supervision and direction of reports required. No instructions needed on routine work and only general instructions given on new lines of work or special assignments. Incumbent may have occasional contact with personnel external to the organizational site. Primary communications are with direct manager, peers, and subordinates, may involve written or oral communication, including obtaining or providing information on matters of moderate to significant importance to the organization, and may be of a sensitive nature. There is responsibility for this position to lead, train, and oversee other supervisors performing similar functions.

PHYSICAL/VISUAL ACTIVITIES OR DEMANDS:

Approximately 30% of time will be spent in the office, 70% of time on the floor with potential exposure to noise and dust. May be required to exert a negligible amount of force continuously and up to 50 pounds of force occasionally to lift, carry, push, pull, or move objects. The job involves sitting, walking, and standing, reaching, talking and hearing. The job involves clarity of vision at 20 inches or less with the ability to bring objects into sharp focus. May need the ability to identify and distinguish colors. Flow of work and character of duties involve normal mental and visual attention much or all of the time. May have exposure to chemicals including acids, bases, organic solvents and inorganic compounds. Chemicals may have characteristic odors or hazardous properties that require special handling. May require wearing a respirator or dust mask.

WORKING CONDITIONS:

24/7 pharmaceutical manufacturing environment with multiple shifts. Requires use of PPE.

DISCLAIMER:

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Employees may be required to follow other job-related instructions and to perform other job-related duties as requested, subject to all applicable state and federal laws. Certain job functions described herein may be subject to possible modification in accordance with applicable state and federal laws. “Commonly associated” is not intended to mean always or only. There are different experiences that suggest other ways or circumstances where reasonable changes or accommodations are appropriate. All activities, demands, conditions and requirements are linked to Essential Job Functions unless marked with an asterisk, which denotes linkage only to marginal function(s).

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.

Come join 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 a global workforce, 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.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Production Supervisor
Production Supervisor

Par Health, Inc. • Greenville (IL)

On-site
USD 70,000 - 95,000
Pharmaceutical Operator I
Pharmaceutical Operator I

Paladin Labs Inc. • Raleigh (NC)

On-site
USD 40,000 - 65,000
Pharmaceutical Operator 1
Pharmaceutical Operator 1

Paladin Labs Inc. • Raleigh (NC)

Hybrid
USD 42,000 - 64,000
Sr. Director, Quality
Sr. Director, Quality

Paladin Labs Inc. • Village of Hobart (NY)

On-site
USD 200,000 - 230,000
Custodian - 2nd Shift
Custodian - 2nd Shift

Paladin Labs Inc. • Village of Hobart (NY)

On-site
USD 19,000 - 25,000
High Volume Plant Technician- 2nd shift
High Volume Plant Technician- 2nd shift

Paladin Labs Inc. • Village of Hobart (NY)

On-site
USD 41,000 - 44,000
Bonus program
Pharmaceutical Operator 1
Pharmaceutical Operator 1

Par Health • North Carolina

On-site
USD 42,000 - 62,000
Pharmaceutical Operator I
Pharmaceutical Operator I

Par Health • United States

On-site
USD 42,000 - 64,000
Chemical Process Operator I (12-Hour Shifts)
Chemical Process Operator I (12-Hour Shifts)

Par Health • North Carolina

On-site
USD 42,000 - 64,000
Executive Director, Supply Chain
Executive Director, Supply Chain

Paladin Labs Inc. • Hazelwood (MO)

On-site
USD 180,000 - 240,000