Technician, Manufacturing V

NCSL International; Chicago (IL); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Vacation and holidays

Medical/dental/vision insurance

401(k)

Short-term incentive programs

Job summary

AbbVie is seeking a skilled professional for cGMP manufacturing in a biologics production setting. You will work with engineers on setup, calibration, rework and quality testing of parts and final materials, using systems like LIMS and SAP to collect data and guide on-line adjustments.

Responsibilities include handling cell culture, chromatography, filtration, buffer prep and equipment prep (CIP/SIP). A BS with 6+ years GMP experience is required, with independent problem-solving and procedural

Qualifications

• BS or equivalent with 6+ years of GMP-relevant experience.
• Capable of independent action and initiative on new assignments.
• Ability to develop and revise procedures.
• Experience assisting supervision in planning area activities.

Responsibilities

• Shipping finished materials.
• Maintaining inventory levels.
• Sampling of in process and raw materials.
• Running glass washer / autoclave.
• Buffer / media preparation.
• Equipment preparation (CIP / SIP).
• Cell culture (from vial thaw to production scale).
• Column chromatography.
• Tangential flow filtration.

Skills

GMP experience

Bioprocess operations

Quality testing

Education

BS in Life Sciences or related field

Tools

LIMS

SAP

Job description

ICompany Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

Performs functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components and final materials. Uses sophisticated programs (such as LIMS, SAP, automated control systems, etc.) to collect and evaluate operating data, which can be used to conduct on-line adjustments to products, instruments or equipment. Determines and may assist in developing methods and procedures to control or modify the manufacturing process.

Responsibilities

• Shipping finished materials.
• Maintaining inventory levels.
• Sampling of in process and raw materials.
• Running glass washer / autoclave.
• Buffer / media preparation.
• Equipment preparation (CIP / SIP).
• Cell culture (from vial thaw to production scale).
• Column chromatography.
• Tangential flow filtration.

Qualifications

• BS (or equivalent experience), with 6+ years area specific relevant experience. (GMP)
• As a highly skilled specialist, contributes to the development of concepts and techniques.
• Completes complex tasks in creative and effective ways.
• Consistently works on complex assignments requiring independent action and a high degree of initiative to resolve issues.
• Makes recommendations for new procedures.
• Acts independently to determine methods and procedures on new assignments.
• Assists Supervisor in planning and leading area activities.

Additional Information

• 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 Company's sole and absolute discretion unless and until paid and may be modified at the Company's 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 https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, visit https://www.abbvie.com/join-us/reasonable-accommodations.htmlI