Machine Operator

ManpowerGroup; Hopkins (MN); Presencial; USD 27.000 - 39.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Weekly overtime hours

Medical and Prescription Drug Plans

Dental Plan

Supplemental Life Insurance

Short Term Disability Insurance

401(k)

Descripción de la vacante

ManpowerGroup is hiring a Medical Production Operator / Manufacturing Technician in Hopkins, MN. The role supports GMP manufacturing and packaging of pharmaceutical products, following GDP and cGMP guidelines.

Tasks include assembly, final packaging, inspection, and strict documentation compliance. The position requires a High School Diploma, about 1 year of equipment operation experience in manufacturing, and the ability to work in a controlled clean room environment with gowning.

Formación

• Must have high school diploma or equivalent.
• Able to work in controlled/clean room environment with gowning.
• Strong documentation and data traceability mindset.
• Excellent communication, verbal and written.
• Attention to detail in fast-paced manufacturing.
• Experience following SOPs in pharma or manufacturing.

Responsabilidades

• Ensure product quality and maintain documentation per GDP/cGMP.
• Receive and distribute materials in manufacturing area.
• Operate manual and automated equipment for assembly, packaging and inspection.
• Move materials within Production area.
• Maintain loading/unloading of materials across stations.
• Reset faults and monitor inputs/outputs on equipment.
• Complete training by due dates.
• Follow SOPs and WI to meet goals and metrics.
• Keep records accurate and compliant with GDP/cGMP.

Conocimientos

Attention to detail

Excellent communication

Organizational & multi-tasking

Microsoft 365 proficiency

Educación

High School Diploma or equivalent

Herramientas

Microsoft 365

Descripción del empleo

Medical Production Operator / Manufacturing Technician – Hopkins, MN

1st shift: 6am-4:30pm, M-Thu

Pay Rate: $24.00

POSITION SUMMARY:

The Manufacturing Technician will be responsible for performing routine tasks for the GMP manufacturing and packaging of pharmaceutical products. This individual is responsible for the documentation and the hands‑on execution of production activities related to assembly, final packaging, and inspection of manufactured pharmaceutical products. This individual operates in accordance with Antares Pharma policies and procedures, environmental, health, safety, and cGMP guidelines.

ESSENTIAL FUNCTIONS AND RESPONSIBILITIES:

• Responsible for quality of products and documentation. Adheres to all manufacturing process and quality requirements.
• Receives and distributes materials and supplies in the manufacturing area.
• Works with manual as well as automated equipment to complete assembly, final packaging, and inspection of pharmaceutical products.
• Moves materials within the Production area.
• Responsible for maintaining uninterrupted loading/unloading of materials and assembled devices from multiple stations of an automated assembly process.
• Interacts with automated equipment to perform basic fault resetting, monitoring of material inputs/outputs and entering setup/run information.
• Completes assigned training prior to due dates.
• Assembles products following all current Standard Operating Procedures (SOPS) and Work Instructions (WIs), while meeting manufacturing goals and metrics.
• Ability to maintain accurate records following Good Documentation Practices (GDP) and current Good Manufacturing Practices (cGMP) guidelines including training files and shop floor paperwork.
• Other duties as assigned

EDUCATION, EXPERIENCE, KNOWLEDGE, SKILLS AND ABILITIES:

• High School Diploma or equivalent is required.
• 1 year of equipment operation and troubleshooting experience in a manufacturing setting.
• Ability to work in a controlled or clean room environment requiring special gowning.
• Critical understanding of the importance of documentation and data traceability.
• Ability to work safely and responsibly in a fast‑paced manufacturing environment.
• Familiarity with executing Standard Operating Procedures (SOPs) in a manufacturing or assembling environment, preferably in the pharmaceutical industry.
• Demonstrates attention to detail.
• Basic computer skills (Microsoft 365)
• Working knowledge of Good Documentation and good Manufacturing Practices preferred
• Ability to work well independently and in a team environment.
• Excellent communication skills, both verbal and written.
• Excellent organizational and multi‑tasking skills
• Able to perform physical activity such as standing for long periods of time, walking, and working with hands.

What's in it for me?

• Opportunity to work in a dynamic and innovative team passionate about positive impact on the lives of patients and their families around the world
• Supportive team culture focused on quality and continuous improvement
• Potential for career growth within a reputable organization
• Opportunity for weekly overtime hours

Upon completion of waiting period associates are eligible for:

• Medical and Prescription Drug Plans
• Dental Plan
• Supplemental Life Insurance
• Short Term Disability Insurance
• 401(k)

ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.