Technician, Pilot Plant IV (2nd shift)
AbbVie
2 months ago
On-site
North Chicago, IL
$18.60 - $33.20 USD yearly
Operations
Job Description
Set up, clean, and maintain equipment. Run processes with supervision and consult appropriate personnel when issues arise. Observe quality characteristics of products and processes. Complete documentation per current Good Manufacturing Practice (cGMP) guidelines and policies.
Responsibilities
- Learn and follow department policies, procedures, and guidelines; complete documentation and supporting data per cGMP.
- Maintain a safe and clean work environment.
- Develop systematic work habits with effective organizational skills.
- Prepare for process requirements following supervisory instruction.
- Note quality issues and address with appropriate people.
- Review procedures and batch records; suggest improvements; identify and help correct safety issues during pre-runs, post-runs, and when reviewing direction sets.
- Provide accurate, complete material and equipment status reports during manufacturing handoffs.
- Learn and use the inventory system.
Qualifications
- High School diploma or GED required; Bachelor’s/Associates in a scientific-related field is desirable.
- Basic technical or mechanical background and knowledge.
- Ability to read, understand, and follow verbal/written operating instructions and equipment/computer monitor processes/flows.
- Ability to write clearly enough to explain process deviations/mistakes.
- Intermediate competency in basic algebra and math involving decimals/fractions and proportions.
- Knowledge and use of tools, machines, instruments, and safety devices used in chemical/pharmaceutical operations; mechanical aptitude and ability to follow written/verbal directions.
Benefits (if eligible)
Paid time off; medical/dental/vision insurance; 401(k); eligible for short-term incentive programs.
Set up, clean, and maintain equipment. Run processes with supervision and consult appropriate personnel when issues arise. Observe quality characteristics of products and processes. Complete documentation per current Good Manufacturing Practice (cGMP) guidelines and policies.
Responsibilities
- Learn and follow department policies, procedures, and guidelines; complete documentation and supporting data per cGMP.
- Maintain a safe and clean work environment.
- Develop systematic work habits with effective organizational skills.
- Prepare for process requirements following supervisory instruction.
- Note quality issues and address with appropriate people.
- Review procedures and batch records; suggest improvements; identify and help correct safety issues during pre-runs, post-runs, and when reviewing direction sets.
- Provide accurate, complete material and equipment status reports during manufacturing handoffs.
- Learn and use the inventory system.
Qualifications
- High School diploma or GED required; Bachelor’s/Associates in a scientific-related field is desirable.
- Basic technical or mechanical background and knowledge.
- Ability to read, understand, and follow verbal/written operating instructions and equipment/computer monitor processes/flows.
- Ability to write clearly enough to explain process deviations/mistakes.
- Intermediate competency in basic algebra and math involving decimals/fractions and proportions.
- Knowledge and use of tools, machines, instruments, and safety devices used in chemical/pharmaceutical operations; mechanical aptitude and ability to follow written/verbal directions.
Benefits (if eligible)
Paid time off; medical/dental/vision insurance; 401(k); eligible for short-term incentive programs.