Production Supervisor

Page Mechanical Group, Inc.; Rosenberg (TX); On-site; USD 40,000 - 80,000; Full time

Job summary

An established industry player in the nutrition sector is seeking a Production Supervisor to lead the production department. This role involves overseeing daily operations, ensuring compliance with FDA regulations, and fostering a safe and productive work environment. The ideal candidate will possess strong leadership and communication skills, with a background in production management. Join a family-owned company committed to excellence and innovation, where your contributions will help shape the future of high-quality nutritional products. Enjoy benefits such as paid time off, health insurance, and career growth opportunities.

Benefits

401(k) with company contribution

Incentive pay

16 days of paid time off

Life and disability insurance

Professional development assistance

Health, dental, and vision insurance

Flexible spending account

Referral program

Career growth path

In-house product allowance

Qualifications

• 2 years of previous or similar work experience is required.
• Must have strong written, verbal, and interpersonal communication skills.
• Ability to lift up to 50 lbs and wear necessary PPE.

Responsibilities

• Supervise production activities to meet FDA regulatory requirements.
• Coordinate new employee orientation, training, and skill advancement.
• Address GMP violations and ensure compliance with OSHA standards.

Skills

Organizational Skills

Time Management

Project Management

Leadership Skills

Communication Skills

Education

High School Diploma or equivalent (GED)

Tools

MS Office (Word, Excel, PowerPoint)

ERP System

Job description

For over 40 years, we have been at the forefront of the nutrition industry, renowned for our top-quality supplements and innovative product delivery systems. Our commitment to advancement is driven by our focus on research initiatives, unique product formulations, and unparalleled quality control. As a family-owned company with a rich history, we take pride in our valued partnerships with healthcare professionals, ensuring that our products meet the highest standards of excellence.

This is a 1^st shift position Monday-Friday 5a-1:30p This position is responsible for supervising the activities of the production department to ensure products are manufactured in accordance with FDA regulatory requirements as well as company procedures and policies.

Essential responsibilities include, but are not limited to the following:

·Supervise personnel; this includes: employee recordkeeping, PTO approval, tracking attendance, performance review, motivating, coaching and working in conjunction with Human Resources to hire, counsel, terminate and address employee related issues.

·Daily supervising all production activities with focus on achieving the daily goals.

·Must be able to assume the responsibilities of production Leads when necessary.

·Assisting production Leads with difficult problem solving and troubleshooting.

·Working directly with the Production Manager to schedule and coordinate manufacturing activities.

·Daily monitoring the productivity of production; making changes, where necessary, to maximize output and maintain successful performance.

·Maintain production operating cost within budget.All overtime must be approved by the Production Manager and justified.

·Working with the Production Manager to develop optimization strategies in order to meet the company’s production needs/goals.

·Maintain and monitor production goals through established key performance indicators (KPI).

·Coordinate and schedule new production employee orientation, training, certification and skill advancement.

·Working with the QA department to resolve quality control issues and assisting with investigations and coordinating the implementation of corrective/ preventative actions.

·Addressing reports of GMP violations and ensuring employees are complying with all regulatory and company policies.

·Supervise the department safety, and ensuring employees are working in compliance with OSHA’s regulatory standards.

·Serve as subject matter expert (SME) for the ERP system with focus on developing production users.

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Work Requirements and Skills

·High School Diploma or equivalent (GED) is required for this position

·2 years ofprevious or similar workexperience is required

·Must have good organizational, time-management, and project management skills

·Must have strong written, verbal, and interpersonal communication skills

·Must have strong leadership skills

·Must have basic computer skills including MS Office applications: Word, Excel, Powder Point and Google mail

·Must demonstrate flexibility when re-prioritization is necessary

·Must be able to work overtime, or a modified schedule, when the company deems it necessary

·Must be able to wear the necessary, job-related personal protective equipment

·Ability to lift (up to 50-lbs), stand, walk, bend, crouch, reach, stretch, step and climb occasionally during the duration of the shift

·Good interpersonal and communications skills, and ability to work effectively in a team-based environment. Perform other related duties as assigned.

Benefits
* 401(k) and contribution from company
* Incentive pay
* 16 days of paid time off and paid holidays
* Life and short/long-term disability insurance
* Professional development assistance
* Health, dental, and vision insurance
* Flexible spending account
* Referral program
* Career growth path
* In-house product allowance