Student Veterans of America Jobs

Welcome to SVA’s jobs portal, your one-stop shop for finding the most up to date source of employment opportunities. We have partnered with the National Labor Exchange to provide you this information. You may be looking for part-time employment to supplement your income while you are in school. You might be looking for an internship to add experience to your resume. And you may be completing your training ready to start a new career. This site has all of those types of jobs.

Here are a few things you should know:
  • This site is mobile friendly. You do not need a log-in or password to access information.
  • Jobs on this site are original and unduplicated and come from three sources: the Federal government, state workforce agency job banks, and corporate career websites. All jobs are vetted to ensure there are no scams, training schemes, or phishing.
  • The site is refreshed daily to remove out-of-date content.
  • The newest jobs are listed first, so use the search features to match your interests. You can look for jobs in a specific geographical location, by title or keyword, or you can use the military crosswalk. You may want to do something different from your military career, but you undoubtedly have skills from that occupation that match to a civilian job.

Job Information

AbbVie Validation Engineer in North Chicago, Illinois

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 (https://twitter.com/abbvieireland) , Facebook, Instagram (https://www.instagram.com/abbvieireland/) , YouTube and LinkedIn.

Job Description

Key Responsibilities

  • Responsible for creation, planning & approval of validation documents to support validation requirements.

  • Responsible for participating in implementation & maintenance of effectiveness of the Quality system to meet applicable regulatory requirements.

  • Adhere to Good Manufacturing Practices (GMPs), ISO:13485, ISO:14971, & 21 CFR 820.

  • Ensure that practices & procedures comply with company policies & applicable regulations for the Quality areas.

  • Execute tasks as required to implement Validation Master Plan & maintain in a validated state the equipment, utilities, facilities, automated process controllers, information systems, cleaning processes, manufacturing process to demonstrate that products will perform consistently as intended.

  • Supervise contract validation resources in the timely completion of activities in his/her area of responsibility.

  • Represent department in quality audits, both internal and external, regarding validation & engineering compliance.

  • Perform Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), & Process Performance Qualification (PPQ).

  • Participate in implementation & maintenance of effectiveness of Quality System to meet all applicable regulatory requirements.

  • Ensure that all practices & procedures comply with company policies & applicable regulations for the Quality areas.

  • Document control of nonconforming products & implementation of corrective & preventative actions (CAPA) to address identified root causes compliant with ISO:13485 standards & 21 CFR 820.90.

  • Execute process monitoring plans based on quantifiable production & quality metrics.

  • Participate with plant & external engineering resources on new installations & systems to ensure that factory, site, & commissioning documentation is in accordance with current Good Manufacturing Practices (“cGMP”) & supports validation.

Qualifications

Must possess a Bachelor’s degree or foreign academic equivalent in Biology, Chemistry, Biomedical Engineering, Mechanical Engineering or related scientific or engineering field plus an academic or industrial background in:

  • Good Manufacturing Practices (GMPs), ISO:13485, ISO:14971, & 21 CFR 820;

  • Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), & Process Performance Qualification (PPQ);

  • documenting control of nonconforming products & implementation of corrective & preventative actions (CAPA) to address identified root causes compliant with ISO:13485 standards & 21 CFR 820.90; &

  • executing process monitoring plans based on quantifiable production & quality metrics.

Apply online at https://careers.abbvie.com/en. Refer to Req ID: REF23813S.


Additional Information

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 and long-term incentive programs.

AbbVie 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.

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