Senior Technician, Stability

North Chicago, IL - USA

Monthly Salary: Not Disclosed

Posted on: 5 hours ago

Vacancies: 1 Vacancy

Job Summary

The Senior QC Technician is responsible for the timely and accurate management of retain stability and reference standard samples in compliance with established policies and procedures for multiple global AbbVie sites and third-party partners. This role demonstrates proficiency in operating multiple systems to execute activities such as receipt storage inspection dispensing and shipping with minimal error. The Senior QC Technician actively implements new technologies and processes assumes ownership of assigned tasks and objectives and independently prioritizes their work schedule to ensure all goals are met.

Responsibilities

Independently works in multiple systems as assigned and can effectively perform a multitude of tasks for which they are trained on with minimal error while adjusting to unforeseen obstacles to accomplish assignments.
Budgets their time effectively to carry out assigned tasks and makes recommendations for improvement. Takes initiative to be involved in team activities and decision making.
Accepts responsibility to complete assigned tasks as committed and proactively identifies and performs new tasks outside area of responsibility.
Maintain stability chambers dispensing laboratory and samples in an orderly audit-ready state
Receive store inspect dispense ship and purge samples according to procedures.
Maintain accurate and thorough documentation.
Communicate with multiple functional groups.
Responsible for compliance with cGMP guidelines DEA controlled substance regulations and maintenance of training requirements.
Responsible for compliance with applicable shipping requirements and record retention for international domestic dangerous goods Occupational Safety and Health Administration and Corporate and Functional policies.
These responsibilities will sometimes require walking over one mile per day and will routinely require standing in place for prolonged periods of 2 hours or more per day. Lifting heavy objects up to 50 lbs. will be required when occasionally handling large shipments of samples. In addition handling of hazardous materials will be required with proper use of personal protective equipment.

Qualifications :

Bachelors degree with 2 years experience in a government regulated pharmaceutical industry or a high school diploma with 5 years of experience in government regulated pharmaceutical industry.
General knowledge of cGMP for documentation and laboratory practices.
Strong attention to detail and organizational skills.
Good interpersonal relations skills verbal and written communication skills.

Additional Information :

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location and we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned vested and determinable. The amount and availability of any bonus commission incentive benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Companys sole and absolute discretion consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

Employment Type :

Full-time

Responsibilities

Independently works in multiple systems as assigned and can effectively perform a multitude of tasks for which they are trained on with minimal error while adjusting to unforeseen obstacles to accomplish assignments.
Budgets their time effectively to carry out assigned tasks and makes recommendations for improvement. Takes initiative to be involved in team activities and decision making.
Accepts responsibility to complete assigned tasks as committed and proactively identifies and performs new tasks outside area of responsibility.
Maintain stability chambers dispensing laboratory and samples in an orderly audit-ready state
Receive store inspect dispense ship and purge samples according to procedures.
Maintain accurate and thorough documentation.
Communicate with multiple functional groups.
Responsible for compliance with cGMP guidelines DEA controlled substance regulations and maintenance of training requirements.
Responsible for compliance with applicable shipping requirements and record retention for international domestic dangerous goods Occupational Safety and Health Administration and Corporate and Functional policies.
These responsibilities will sometimes require walking over one mile per day and will routinely require standing in place for prolonged periods of 2 hours or more per day. Lifting heavy objects up to 50 lbs. will be required when occasionally handling large shipments of samples. In addition handling of hazardous materials will be required with proper use of personal protective equipment.

Qualifications :

Bachelors degree with 2 years experience in a government regulated pharmaceutical industry or a high school diploma with 5 years of experience in government regulated pharmaceutical industry.
General knowledge of cGMP for documentation and laboratory practices.
Strong attention to detail and organizational skills.
Good interpersonal relations skills verbal and written communication skills.

Additional Information :

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location and we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.

AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

Employment Type :

Full-time

Key Skills

Computer Operation
Computer Skills
Generator Repair
Military Experience
Mechanical Knowledge
Commercial Driving
HVAC/R
Ftp
Schematics
Maintenance
Medical Imaging
Troubleshooting

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About Company

AbbVie

AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuro ... View more

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