Job Summary

We are seeking a dedicated, detail-oriented OSD Production Operator for our second-shift operations. The successful candidate will perform solid-dosage manufacturing activities, including dispensing, granulation, sifting, milling, drying, encapsulation, coating, and compression. This role requires accurate documentation, adherence to Standard Operating Procedures (SOPs), and the ability to work effectively in a cGMP environment. The operator will collaborate with site support personnel and management to help ensure efficient, timely production.

Key Responsibilities

• Perform solid-dosage manufacturing processes, including dispensing, granulation, sifting, milling, drying, encapsulation, coating, and compression.
• Complete scheduled commercial and non-commercial manufacturing activities on time.
• Develop proficiency in setting up, operating, and cleaning cGMP equipment used in production.
• Complete all required batch record documentation accurately and legibly.
• Read, understand, and follow documented SOPs, batch records, and safety procedures.
• Maintain a clean, organized cGMP work area and follow good housekeeping practices.
• Participate in quality investigations as required.
• Use required personal protective equipment (PPE) during cGMP activities.

Qualifications

Skills

• Familiarity with a regulated pharmaceutical solid-dosage facility.
• Ability to read and write documents in English.
• Strong written communication skills.
• Familiarity with cGMP solid-dosage pharmaceutical manufacturing equipment.
• Ability to set up, operate, clean, and troubleshoot pharmaceutical manufacturing equipment.
• Ability to work with minimal supervision.
• Ability to stand for an eight-hour workday.
• Ability to lift up to 30 lb (14 kg) without assistance.
• Ability to maintain personal hygiene consistent with a cGMP environment.
• Ability to wear all required PPE, including partial- and full-face respirators.

Education

• High school diploma or GED equivalent.
• A bachelor’s degree in physical sciences or a pharmaceutical or life-science-related field is preferred.

Attributes

• Detail-oriented
• Reliable and punctual
• Team player
• Strong work ethic
• Ability to follow instructions precisely

Benefits

• Competitive hourly wage for second-shift operations.
• Opportunity to work in a regulated pharmaceutical manufacturing environment.
• Comprehensive training on cGMP processes and equipment.
• Potential for career growth within the company.

How to Apply

Interested candidates can submit their application using the “Apply Now” button.