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 $30,524 as of June 27, 2024, but the range typically falls between $26,689 and $34,359. 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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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.
YOU BRING:
PDN2
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