Pharmaceutical Manufacturing Operator

Warker LLC; Scottsdale (AZ); On-site; USD 55,000 - 75,000; Full time

Job summary

Warker LLC is seeking an Operator II to support biotech and pharmaceutical production in a regulated environment in Scottsdale, AZ. The role requires operating and monitoring manufacturing and/or lab equipment in GMP-compliant procedures and accurately recording all activities.

You will prepare materials, perform routine equipment checks, support quality control activities, troubleshoot routine issues, and maintain a safe, clean, and compliant workspace.

Qualifications

• GMP knowledge and documentation discipline.
• Ability to operate manufacturing/lab equipment safely.
• Strong attention to detail.
• Basic troubleshooting skills.
• Effective teamwork in a regulated setting.

Responsibilities

• Prepare materials and support production/lab workflows.
• Perform routine equipment and process checks.
• Support quality control activities, including routine testing support.
• Troubleshoot routine issues and escalation as needed.
• Maintain a safe, clean, and compliant work area.
• Collaborate with cross-functional teams to meet production requirements.
• Contribute to continuous improvement while maintaining safety, quality, and patient impact standards.

Skills

GMP compliance

Equipment operation

Attention to detail

Troubleshooting basics

Team collaboration

Job description

Operator II supporting biotech and pharmaceutical production in a regulated environment.
Operate and monitor manufacturing and/or lab equipment, ensuring adherence to GMP-compliant procedures. Accurately record and document all activities.

• Prepare materials and support production/lab workflows
• Perform routine equipment and process checks
• Support quality control activities, including routine testing support
• Troubleshoot routine issues and escalation as needed
• Maintain a safe, clean, and compliant work area
• Collaborate with cross-functional teams to meet production requirements
• Contribute to continuous improvement while maintaining safety, quality, and patient impact standards

Key qualifications/skills

strong GMP and documentation discipline, ability to operate equipment safely, attention to detail, basic troubleshooting skills, and effective teamwork in a regulated setting.