ABBVIE INC Operations Associate III Salary in the United States

How much does a Operations Associate III make at companies like ABBVIE INC in the United States? The average salary for Operations Associate III at companies like ABBVIE INC in the United States is $30,447 as of May 28, 2024, but the range typically falls between $26,623 and $34,270. Salary ranges can vary widely depending on many important factors, including education, certifications, additional skills, the number of years you have spent in your profession. With more online, real-time compensation data than any other website, Salary.com helps you determine your exact pay target.  View the Cost of Living in Major Cities

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What does a Operations Associate III do at companies like ABBVIE INC?

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 www.abbvie.com. 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/associates to work at our Campbell site.  Be Bold and grow your manufacturing biopharmaceutical career with the pharmaceutical and medical device industry leader!

Operations Analyst III- Biopharmaceutical/GMP

An “ideal” candidate for this role is someone with sound knowledge of the biopharmaceutical manufacturing environment with hands on experience in fermentation and purification and experience in regulatory requirements.

 

Successful candidates will have the following types of experience:

  • The manufacture of marketed drug substance

  • Implementing improvements to the equipment, procedures and systems used in Manufacturing

  • Support of ongoing clinical products and projects related to new product introduction and technical transfer

     

     

YOU WILL:

Be a trusted and expert partner.   Technical expertise should include thorough knowledge of biopharmaceutical manufacturing technology and regulatory requirements, normally acquired through a progressive operation experience in a GMP environment. Especially critical is high level knowledge and experience in the areas of microbiology, fermentation, aseptic processing, and protein purification techniques.

Be a compliance expert.  Completion and review of Manufacturing documentation.  This includes forms, batch production records and any other quality system documentations.   You will improve the technical capabilities and quality practices within the department. Coordinate activities and resolve issues across the department, other groups, and/or projects.  You will respond to and/or resolve recurring technical or processing issues.  Develop and implement novel approaches to solving non-routine technical problems.  Communicate information effectively through updates, reports, and summaries. You will lead improvements in processes and methods that reinforce cGMP within the department and/or across the site.


Innovate for the future.    Apply systematic thinking processes and technical knowledge to independently address a broad range of non-routine to moderately complex problems.  You will conduct investigations, demonstrate strong technical and problem-solving skills, and excellent technical writing skills.  You will provide training and guidance to the staff to meet the goals of the department.  When appropriate, assist in providing leadership on project teams.  The position will need to be experienced in project management oversight including overseeing the capital expenditure projects and function as a project manager.

 




Qualifications

YOU BRING:

   

  • BS in Science or Engineering field or Associate’s Degree and equivalent years of experience
  • Three years working in a GMP environment, Pharmaceutical industry preferred
  • Two years of hands on experience of fermentation, purification or pharmaceutical manufacturing process
  • Thorough knowledge of biopharmaceutical manufacturing technology and regulatory requirements,
  • Previous experience in facility or systems modification / design, as well as specifying equipment, creating systems and Standard Operating Procedures (SOPs)

 

 

 

 PDN2

 



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.
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$26,623 Low Average $30,447 High $34,270

Understand the total compensation opportunity for Operations Associate III at companies like ABBVIE INC, base salary plus other pay elements

Average Total Cash Compensation

Includes base and annual incentives

$26,623
$34,270
$30,447
The chart shows total cash compensation for the ABBVIE INC Operations Associate III in the United States, which includes base, and annual incentives can vary anywhere from $26,623 to $34,270 with an average total cash compensation of $30,447. Total compensation includes the value of any benefits received in addition to your salary and some of the benefits that are most commonly provided within a total compensation package including bonuses, commissions, paid time off, and Insurance. The total cash compensation may get paid differently by industry, location, and other factors.
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