Technician, Manufacturing II (Wednesday to Saturday, 4:00pm-2:30am)

AbbVie Inc.

Worcester (MA)

Vor Ort

USD 60.000 - 90.000

Vollzeit

vor 41 Stunden
Sei unter den ersten Bewerbenden

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Zusammenfassung

AbbVie Inc. in Worcester, MA, is seeking a manufacturing professional to support cGMP operations in a biologics production setting.

You will work with engineers on set-up and calibration tasks and perform rework and quality testing to ensure production of parts, components and final materials. Responsibilities include shipping finished materials, maintaining inventory, sampling materials, operating glass washer and autoclave, preparing buffers and media, CIP/SIP prep, and handling cell culture

Qualifikationen

  • Associates degree in science or equivalent experience; BS in science with 1+ years relevant experience; BS in engineering with 0+ year relevant experience.
  • BS with 1+ years relevant experience.
  • BS in Engineering with 0+ year relevant experience.

Aufgaben

  • 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.

Kenntnisse

cGMP manufacturing
Process understanding

Ausbildung

Associate degree in science
BS in Science
BS in Engineering

Tools

LIMS
SAP
Automation systems

Jobbeschreibung

Company 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
  • Associates degree in science (or equivalent experience), with 2+ years relevant experience. BS, with 1+ years relevant experience.BS in Engineering, with 0+ year relevant experience.
  • Applies acquired job skills and company policies and procedures to complete assigned tasks.
  • Works on assignments that are semi-routine in nature but recognizes the need for occasional deviation from accepted practice.
  • Normally follows established procedures on routine work, requires instructions only on new assignments.
Additional Information

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

  • The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at thetimeofthis posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographiclocation,andwemayultimatelypaymore or less than the posted range. This range may bemodifiedin thefuture.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.
  • This job is eligible toparticipatein our short-term incentiveprograms.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.Theamountandavailabilityof anybonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employeeremainsin the Company'ssoleandabsolutediscretion unless and until paid andmay bemodifiedat the Company’s sole and absolute discretion, consistent withapplicable 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, click here to learn more:

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

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