Pharma Process Operator I – Micronizing & Milling

Ampcus Inc; Malvern (Chester County); On-site; USD 42,000 - 65,000; Full time

Job summary

Ampcus is seeking a Manufacturing - Process Operator I in Malvern to join our sterile manufacturing team. The role performs micronization and milling of pharmaceutical actives and excipients, following client Malvern procedures and cGMP guidelines.

You will set up and operate equipment, document batch records, work in a regulated environment, and support continuous improvement while complying with safety and PPE requirements.

Qualifications

• High School Diploma or GED.
• Must be dependable, ready/eager to learn and able to meet the physical requirements of the job.
• Prior manufacturing experience and work in a regulated environment preferred.
• Ability to work weekday and weekend overtime a plus.
• Technical Skills/Knowledge including Communication Skills, Basic Math Skills, and interpretation.
• Potential limited exposure to health and physically hazardous chemicals.
• Personal protective equipment is provided and required in designated areas.
• Physical strength, stamina, and dexterity required. Lift up to 44 lbs.
• Ability to work safely with HPAPI.
• Prolonged standing, lifting, bending, and climbing as part of moderate physical labor.
• Work in loud environments with hearing protection.

Responsibilities

• Perform entry-level micronization and milling of actives and excipients.
• Set up, operate equipment, and monitor production processes.
• Report production on batch records following GDPs.
• Work in a regulated environment with SOP adherence.
• Identify and communicate deviations and GMP deficiencies to supervisor.
• Maintain clean processing areas and equipment.

Skills

Communication Skills

Basic Math Skills

Interpretation

Education

High School Diploma or GED

Job description

Ampcus is seeking a Manufacturing - Process Operator I in Malvern to join our sterile manufacturing team. The role performs micronization and milling of pharmaceutical actives and excipients, following client Malvern procedures and cGMP guidelines.

You will set up and operate equipment, document batch records, work in a regulated environment, and support continuous improvement while complying with safety and PPE requirements.