*Quality Control Analyst

Campbell, CA, United States
Sep 29, 2020
Quality, Quality Control
Required Education
Bachelors Degree
Position Type
Full time
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines 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, eye care, virology, women's health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . Follow @abbvie on Twitter , Facebook , Instagram , YouTube and LinkedIn .

Job Description

Envision working with energetic colleagues and inspirational leaders. AbbVie is always striving to find top scientists to work at our Campbell, CA site. Be Bold and grow your manufacturing biopharmaceutical career with the pharmaceutical and medical device industry leader!

Quality Control Analyst - Campbell, CA

What your manager wants you to know:

"I am looking for a team player with Quality Control analytical chemistry experience in a cGMP environment. If you are motivated, organized, have strong communication and written skills, I would be very interested in receiving your resume. Let's discuss what you can bring to the team."

Successful quality control analyst candidates will contribute by:

Providing analytical support for the manufacture, release, and stability testing of drug substance produced at AbbVie DSO. You will contribute to the completion of milestones associated with specific Quality projects.

  • Be a trusted and expert partner. Provide analytical support for the manufacture, release, and stability testing of drug substance produced at DSO. This includes regulatory compliance and validation activities. You will provide GMP systems support including software support and SOP maintenance.
  • Build bridges. You will conduct and write investigation and you will be managing projects that include equipment qualification and method transfer. You will be assigned additional projects as business needs arise.

  • Detailed compliance master. You will work to ensure that the company is in compliance with all environmental, health and safety requirements and assure our business practices enhance the welfare of our customers, employees and the community in which we operate. You have full authority to make decisions and/or take actions required to carry out your job duties. AbbVie internal requirements include compliance with ethics, environmental health and safety, financial, human resources, cGMP procedures, general business policies, requirements, and objectives. AbbVie is a regulated company and the incumbent is expected to be fully compliant with all criteria established by governmental agencies, Ministry of Health, and legislative requirements including, but not limited to: the FDA, European Community (EC), ISO 13485 - Medical Devices, European Economic Community Medical Device Directive (MDD), Canadian Medical Device Regulations (CMDR), OSHA, Sarbanes-Oxley, EPA, DOT, EEOC, and ADA.


  • BS in Chemistry/Biochemistry or a related Biological Science field
  • 2+ years of relevant pharmaceutical industry and 1 plus year(s) of GMP experience
  • Strong user of Track Wise, Microsoft Project, Excel, Words, Empower, LabWare, Compliance Wire
  • Prefer experience in protein chemistry, wet chemistry, USP/EP monographs
  • Excellent analytical skills and effective problem-solving skills.
  • Excellent written documentation skills.
  • Hands-On experience with HPLC, GC, Gels, and wet chemistry techniques.
  • Familiar with the USP, EP, JP, and CP compendial.


Equal Employment Opportunity
At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis 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, protected veteran status, or any other legally protected characteristic.