Compounding Manufacturing Operator

ROIS; Phoenix (AZ); On-site; USD 30,000 - 43,000; Full time

Job summary

ROIS in Phoenix, AZ is seeking a motivated Compounding Manufacturing Operator. This entry-level role offers training and exposure to a highly regulated pharmaceutical environment with emphasis on quality and compliance.

You will perform manufacturing activities following detailed procedures, handle hazardous materials safely, maintain accurate documentation, and participate in continuous improvement initiatives while developing a long-term career in pharmaceutical manufacturing.

Qualifications

• High School Diploma or equivalent.
• 1+ year of experience in GMP-regulated cleanroom or similar.
• Strong attention to detail and ability to follow written procedures exactly.
• Willingness to learn and develop a long-term career in pharmaceutical manufacturing.
• Ability to stand for extended periods and lift 20+ lbs.
• Must wear PPE including respirators when required.

Responsibilities

• Accomplishes manufacturing activities per detailed procedural guidance with attention to detail.
• Performs handling of hazardous materials in compliance with regulations.
• Executes responsibilities mandated by written procedures and regulations.
• Maintains accurate documentation and addresses errors promptly.
• Participates in ongoing job-specific training requirements.
• Contributes to continuous improvement (CI) projects.

Skills

Attention to detail

Written procedures

Documentation

Eager to learn

Education

High School Diploma or equivalent

Job description

Schedule: Monday - Thursday | 2:00pm - 12:30am

Pay: $22.00 - $31.25/hourly *Depending on experience* + 15% Shift Differential

We are seeking a motivated individual interested in a career in the pharmaceutical industry. This is an Compounding Manufacturing Operator role where we are willing to train candidates who have experience working in cleanroom, sterile, laboratory, or other highly controlled environments.

The ideal candidate is eager to learn, follows procedures exactly as written, takes documentation seriously, and understands the importance of quality and compliance in a regulated manufacturing setting.

Responsibilities:

• Accomplishes manufacturing activities per detailed procedural guidance with a demonstrated attention to detail.
• Performs handling of hazardous materials in compliance with site, industry, local, and federal regulations.
• Executes specialized responsibilities mandated by detailed written procedures, site, industry, local, and federal regulations.
• Assures and completes detailed documentation that is a correct and accurate record. Addresses procedural and documentation errors expeditiously and effectively.
• Continuously updates job knowledge by participating in job specialized training requirements.
• Participate as a contributing member in continuous improvement (CI) projects.
• Consistently projects a positive attitude and example for other department team members/operators to emulate.
• Performs other tasks as assigned.

Requirements:

• High School Diploma or equivalent.
• Demonstrated job stability on resume.
• 1+ year of experience in a GMP-regulated, cleanroom, food manufacturing, healthcare, laboratory, or similarly controlled environment.
• Strong attention to detail and ability to follow written procedures exactly.
• Comfortable working in a highly regulated environment where documentation and compliance are critical.
• Eager to learn, receive coaching, and develop a long-term career in pharmaceutical manufacturing.
• Positive attitude and strong work ethic.
• Ability to stand and remain active for extended periods throughout the shift.
• Ability to frequently lift, push, pull, and move materials weighing 20+ lbs.
• Comfortable performing extensive cleaning and sanitization activities throughout the day.
• Able to work while wearing required cleanroom gowning and personal protective equipment (PPE), including respirators when required.