Solid Dose Operator I

Job Overview

Employee Job Description

Job Title: Solid Dose Operator I

Date Prepared:08/08/2026

Department/Division: Production Reporting Relationship: Production Manager

Location of Position: Batesville, AR Date of Last Revision: 08/08/2026

Exemption Status: Non-exempt Safety Sensitive: Yes

Job Summary:

The Solid Dose Operator I is responsible for performing assigned manufacturing activities within either the tablet compression or capsule filling function of the Solid Dose department. This position supports the production of high-quality nutritional products by operating, monitoring, cleaning, and maintaining solid dose manufacturing equipment in accordance with approved batch records, Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMP), applicable FDA requirements, and company quality and safety standards.

The Solid Dose Operator I is expected to develop and maintain proficiency within their assigned specialty, including equipment setup, operation, changeovers, cleaning, basic adjustments, process monitoring, in-process testing, and completion of required production documentation. The position is responsible for verifying materials and equipment, maintaining product traceability, identifying process or equipment concerns, and ensuring products are manufactured consistently and according to established specifications.

This position works closely with Production, Quality Assurance, Maintenance, Warehouse, and other support teams to meet production schedules and maintain a safe, efficient, and compliant manufacturing environment. Success in this role requires attention to detail, mechanical aptitude, reliability, willingness to learn, and a commitment to safety, quality, productivity, and continuous improvement.

Success in this role requires accuracy, reliability, sound judgment, effective communication, technical proficiency, and the ability to work independently while maintaining high standards of safety, quality, compliance, and operational efficiency.

Note: This job description has been designed to indicate the general nature and level of work performed by employees in this position. It is not interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job.

Duties and Responsibilities:

Condition of employment requires knowledge and conformance to Standard Operating Procedures (SOPs) and Good Manufacturing Practices (cGMPs) as applicable to the position.

Perform assigned tablet compression or capsule filling operations according to approved batch records, SOPs, and production requirements.

Verify correct materials, product information, equipment, tooling, machine components, and batch documentation prior to production.

Perform equipment setup, assembly, disassembly, cleaning, and changeovers within the assigned specialty.

Load and handle raw materials and work-in-process materials according to established procedures.

Operate and monitor tablet presses or capsule filling equipment to maintain consistent production and product quality.

Perform routine machine adjustments within established procedures and training.

Monitor equipment performance and product characteristics during production.

Perform required in-process quality checks, such as tablet weight, appearance, hardness, thickness, or capsule fill weight.

Identify and promptly report equipment malfunctions, process deviations, material concerns, or product quality issues.

Perform basic troubleshooting within the scope of training and established procedures.

Complete batch records, equipment logs, cleaning records, and other required production documentation accurately and timely.

Maintain accurate product identification, traceability, and material accountability throughout production.

Perform line clearance and equipment verification activities to prevent product mix-ups and cross-contamination.

Follow established procedures for handling raw materials, tablets, capsules, and work-in-process materials.

Clean and sanitize equipment, tools, and production areas according to established procedures.

Maintain a clean, organized, and GMP-compliant manufacturing environment.

Support preventive maintenance and equipment maintenance activities as directed.

Communicate production status, equipment conditions, material needs, and concerns to the appropriate supervisor.

Participate in training and cross-training activities as required.

Support continuous improvement efforts focused on safety, quality, efficiency, productivity, and waste reduction.

Support internal and external audits by maintaining accurate documentation and following established procedures.

Assist other production areas as needed to meet departmental goals.

Perform other duties as assigned by management.

Contacts and Relationships:

Internal Customers

All Lifeplus employees

Production and Operations teams

Quality Assurance and Quality Control personnel

Maintenance and Facilities teams

Warehouse and Inventory Control personnel

Planning and Scheduling teams

Executive Leadership Team

External Customers

Equipment manufacturers and service providers

Regulatory auditors and inspectors

Technical consultants and contractors

Accountability:

Direct accountability to the Production Manager

Qualifications and Guidelines:

Experience/Training/Education

High school diploma or GED equivalent preferred.

Previous manufacturing experience in pharmaceutical, nutraceutical, food, or other regulated production environments preferred.

Experience operating tablet presses, capsule filling machines, or similar manufacturing equipment preferred.

Experience with equipment setup, changeovers, cleaning, and basic troubleshooting preferred.

Ability to read and follow batch records, SOPs, work instructions, and manufacturing procedures.

Ability to complete required GMP, safety, quality, and equipment training.

Ability and willingness to develop technical proficiency within the assigned specialty.

Knowledge Of:

Basic principles of tablet compression or capsule filling.

Operation and adjustment of equipment within the assigned specialty.

Solid dose manufacturing processes and production workflows.

Equipment setup, changeovers, cleaning, and basic troubleshooting.

Batch records, production documentation, and product traceability requirements.

cGMP, SOPs, quality standards, and contamination prevention practices.

In-process quality testing and product inspection requirements.

Safe handling of raw materials and solid dose products.

GMP sanitation and housekeeping requirements.

Workplace safety practices and PPE requirements.

Skills/Abilities:

Ability to safely operate equipment within the assigned specialty.

Mechanical aptitude and ability to learn equipment operation and adjustments.

Strong attention to detail and commitment to product quality.

Ability to recognize and report equipment or process issues.

Ability to interpret batch records, SOPs, and production instructions.

Ability to accurately complete manufacturing documentation.

Ability to work independently within established procedures and as part of a production team.

Strong communication and problem-solving skills.

Commitment to safety, compliance, quality, and continuous improvement.

Physical Requirements/Working Conditions:

Rarely (1-10%) Occasionally (11-33%) Frequently (34-66%) Continuously (67%+)

Sitting O* KneelingR*

Standing F* ClimbingR*

Bending F* ReachingO*

Lifting F (60 lbs) Grasping/handling F

Turning/twisting O* SquattingR*

Pay: $1.00 - $15.00 per hour

Expected hours: 40.0 per week

Work Location: In person