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Manufacturing Technician III - 6am - 4:30pm - Wednesday - Saturday

Allergan

North Chicago (IL)

On-site

USD 50,000 - 90,000

Full time

30 days ago

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Job summary

An established industry player is seeking a dedicated professional to join their biologics production facility. This role involves performing critical functions in cGMP manufacturing operations, including quality testing and data evaluation using sophisticated programs. You will be responsible for maintaining inventory, preparing buffers, and conducting cell culture processes. Join a team that values innovation and integrity, where your contributions will directly impact the health and well-being of individuals across various therapeutic areas. If you are passionate about making a difference in the healthcare sector, this opportunity is for you.

Benefits

Paid time off
Medical insurance
Dental insurance
Vision insurance
401(k) plan

Qualifications

  • 4+ years of relevant experience in cGMP manufacturing.
  • Understanding of manufacturing processes and quality control.

Responsibilities

  • Shipping finished materials and maintaining inventory levels.
  • Performing sampling of in-process and raw materials.

Skills

cGMP manufacturing operations
quality testing
data evaluation
problem-solving

Education

Associate's degree in science
Bachelor's degree in relevant field

Tools

LIMS
SAP
automated control systems

Job description

Company Description

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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.


Job Description

Purpose

Describe the primary goals, objectives or functions or outputs of this position.

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.
  • Hours- 6am - 4:30pm - Wednesday - Saturday.

Qualifications

Qualifications

  • Associates degree in science (or equivalent experience), with 4+ years area specific relevant experience. Bachelor's Degree with 2+ years area specific relevant experience.
  • Has substantial understanding of the job and applies knowledge and skills to complete a wide range of tasks.
  • Works on assignments that are moderately difficult, requiring judgment in resolving issues or in making recommendations.
  • Normally receives little instruction on daily work, general instructions on newly introduced assignments.
  • May be informal team leader.

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 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, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

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, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

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