Pharmaceutical Manufacturing Operator – Solid Dosage

Senior Pharmaceutical Manufacturing Operator – Solid Dosage (Tablets & Capsules)

Job Type Full-Time

Job Summary

We are seeking an experienced Pharmaceutical Manufacturing Operator to support solid dosage manufacturing operations in a regulated cGMP environment. The ideal candidate will have hands-on experience with tablet and capsule manufacturing processes, including dispensing, granulation, sifting, milling, drying, encapsulation, coating, compression, and equipment cleaning.

This position requires strong knowledge of pharmaceutical manufacturing procedures, cGMP compliance, SOP adherence, and production documentation. Candidates must demonstrate job stability and the ability to work independently while maintaining high standards of quality, safety, and efficiency.

Key Responsibilities

• Perform solid dosage manufacturing activities including:
• Dispensing
• Granulation
• Sifting
• Milling
• Drying
• Encapsulation
• Coating
• Tablet Compression
• Equipment Cleaning
• Set up, operate, monitor, troubleshoot, and clean pharmaceutical manufacturing equipment.
• Complete batch records and production documentation accurately and legibly.
• Follow all cGMP regulations, Standard Operating Procedures (SOPs), Batch Records, and safety requirements.
• Support commercial and non-commercial manufacturing activities to ensure production schedules are met.
• Maintain cleanroom and manufacturing areas according to housekeeping and compliance standards.
• Participate in quality investigations and corrective actions when required.
• Wear and properly utilize all required PPE in accordance with OSHA and company guidelines.
• Collaborate with Production, Quality, and Operations teams to ensure compliant manufacturing processes.

Required Qualifications

• Minimum 3 years of experience working for a pharmaceutical manufacturing company.
• Minimum 2–3 years of recent experience as a Production Operator or Manufacturing Operator in pharmaceutical manufacturing.
• Experience working in a regulated cGMP pharmaceutical environment.
• Hands-on experience with solid oral dosage manufacturing (tablets and capsules).
• Strong understanding of:
• Dispensing
• Granulation
• Sifting
• Milling
• Drying
• Encapsulation
• Coating
• Compression
• Cleaning Processes
• Experience operating and cleaning pharmaceutical manufacturing equipment.
• Ability to read, understand, and follow SOPs, batch records, and manufacturing instructions.
• Strong written documentation skills.
• Ability to work with minimal supervision.
• Demonstrated job stability with consistent employment history.

Preferred Qualifications

• Experience with multiple solid dosage manufacturing processes and equipment.
• Experience participating in quality investigations and deviation management.
• Strong understanding of pharmaceutical manufacturing best practices and regulatory compliance.

Education

• High School Diploma or GED required.
• Bachelor's Degree in Physical Sciences, Pharmaceutical Sciences, Life Sciences, or a related field preferred.

Physical Requirements

• Ability to stand for extended periods throughout an 8-hour shift.
• Ability to lift up to 30 lbs. (14 kg) without assistance.
• Ability to wear required PPE, including partial and full-face respiratory protection when necessary.
• Maintain personal hygiene standards required for cGMP manufacturing environments.

Skills: granulation,pharmaceutical manufacturing,manufacturing