$28 - $36 per hr

5 month contract (through mid-May) initially, possible to extend based on need

1st shift, M-F 8-5 pm

**2+ years of manufacturing experience in pharma/device is required**

PRIMARY RESPONSIBILITIES:

• Ensure the product is being manufactured with strict adherence to all Manufacturing, Quality, Safety and Environmental SOPs.

• Set up, operate, monitor, clean, and maintain various processing, packaging and testing equipment.

• Assist in certain maintenance activities to ensure routine preventative maintenance, and calibrations are performed in a timely manner with minimal impact on processing schedules and complete adherence to procedures and Quality, Safety and Environmental guidelines.

• Ensure that batch records and all associated process documentation are completed as they occur and done right the first time by utilizing manufacturing and documentation policies and procedures.

• Continuously evaluate processes with regard to quality, safety, environmental, and productivity enhancements.

• Maintain good housekeeping within their work area.

• Notify supervisor of any issues that can negatively impact compliance, safety, or productivity.

• Assist other departments when reasonable and necessary tasks are required for compliance, efficiency, etc.

• Communicate batch / equipment status and issues to supervisor and other operators. Actively participate in manufacturing meetings.

• Participate in process improvement and cost saving initiatives

• Train in all areas (manufacturing and packaging) in order to successfully rotate between the functional duties and support changing production needs

• Keep current on all required training.

• Assist with project work or inventory management duties during downtime between production runs.

EDUCATIONAL PREREQUISITES AND SKILL REQUIREMENTS:

• High School diploma or general education degree (GED) is required. Some experience working with medical device or pharmaceutical liquid dose manufacturing equipment and processes helpful.
• 3-5 Years of manufacturing experience, medical device/ pharmaceutical manufacturin
• Ability to read and write in the English language. Ability to read and follow standard operating procedures and work instructions.
• Physical Demands and Work Environment: Ability to stand for extended periods of time
• Ability to lift and maneuver up to 50 pounds

TRAINING REQUIREMENTS:

• Undergo all formal Training Events as may be directed from time-to-time.

• Observe and comply with all Corporate Policies.

• Work within, and ensure adherence to Quality System procedures, work instructions and other Quality System requirements.

• Work within, and ensure adherence to Health, Safety and Environment Management System procedures, instructions and other requirements.