Manufacturing Operator

ROIS; Phoenix (AZ); Presencial; USD 39.000 - 48.000; Jornada completa

Descripción de la vacante

ROIS in Phoenix, AZ is seeking a Manufacturing Operator (Packaging Operator I) to support production of sterile injectable products in a regulated environment. You will follow detailed work instructions, maintain GMP/SOP compliance, and help ensure safety and quality.

The schedule is Monday-Thursday, 6:00am-4:30pm. This role requires lifting, gowning in controlled areas, accurate documentation, and teamwork with cross-functional groups to meet production goals.

Formación

• High school diploma or GED required; equivalent combinations considered.
• Experience in regulated manufacturing or GMP environment preferred.
• Ability to read, write and understand English; basic math skills.

Responsabilidades

• Follow detailed work instructions and production procedures.
• Prepare equipment, materials, and resources to meet schedules.
• Operate and support sterile injectable manufacturing equipment.
• Handle hazardous materials per regulations and policies.
• Document production activities accurately in real time per GMP.
• Identify and address discrepancies in procedures or documentation.
• Participate in training and continuous improvement initiatives.
• Collaborate with team members and cross-functional departments.

Conocimientos

Attention to detail

Documentation accuracy

Written communication

Verbal communication

Mathematical skills

English literacy

Teamwork

Flexibility/OT

Independent work

Educación

High School Diploma or GED

Equivalent education/experience

Herramientas

Microsoft Office

MES/HMI/Manufacturing software

Descripción del empleo

Job Title: Manufacturing Operator (Packaging Operator I)

Location: Phoenix, AZ

Schedule: Monday - Thursday | 6:00am - 4:30pm

Pay: $28.00 - $34.61/hourly

We are seeking a motivated Manufacturing Operator to support the production of sterile injectable pharmaceutical products in a regulated manufacturing environment. This role is critical to ensuring products are manufactured safely, efficiently, and in full compliance with current Good Manufacturing Practices (cGMPs), Standard Operating Procedures (SOPs), and regulatory requirements.

This position is ideal for individuals who thrive in a fast-paced manufacturing environment, enjoy hands-on work, and are committed to quality, safety, and teamwork.

Job Responsibilities:

• Execute manufacturing activities by following detailed work instructions and production procedures.
• Ensure equipment, materials, and production resources are prepared and available to meet manufacturing schedules.
• Operate and support specialized manufacturing equipment used in sterile injectable production.
• Handle hazardous materials in compliance with company policies and local, state, and federal regulations.
• Complete production documentation accurately and in real time, ensuring all records meet GMP requirements.
• Identify and promptly address procedural or documentation discrepancies.
• Participate in required training programs to maintain and improve job-related knowledge and skills.
• Support continuous improvement initiatives and operational excellence projects.
• Collaborate effectively with team members and cross-functional departments.
• Maintain a positive, safety-focused, and quality-driven work environment.
• Perform additional duties as assigned.

Qualifications:

• Successful completion of annual TITMUS vision testing.
• Respiratory medical screening clearance.
• At least 1 year of experience in a regulated manufacturing or GMP environment preferred.
• High School Diploma or GED required.
• Equivalent combinations of education and experience will be considered.
• Standing for extended periods, up to 8 hours per shift.
• Pushing, pulling, reaching, balancing, and lifting more than 20 pounds on a regular basis.
• Working in controlled manufacturing environments and around chemical agents or hazardous materials.
• Ability to successfully gown for controlled manufacturing areas.
• Flexibility to work overtime, alternate shifts, weekends, or adjusted schedules based on business needs.
• Working knowledge of Microsoft Office applications and computerized manufacturing systems such as MES, HMI, or similar platforms.
• Strong attention to detail and commitment to documentation accuracy.
• Effective written and verbal communication skills.
• Basic to intermediate mathematical skills.
• Proficiency in reading, writing, and understanding English.
• Mechanical aptitude and the ability to use hand tools for equipment setup and troubleshooting.
• Ability to work independently and collaboratively in a team environment.
• Understanding of GMP-regulated manufacturing environments preferred.

Additional Information

• Travel required: Less than 10%.
• Schedule flexibility, shift work, and overtime may be required to support production needs.