What AbbVie Has to Offer:
Our work can—and does—have a tangible, lasting impact on millions of people. But it’s not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.
Our work can—and does—have a tangible, lasting impact on millions of people. But it’s not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.
Job details
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, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.
Key Responsibilities
- Lead manufacturing projects to enhance process efficiency, yield, quality, cycle time, & cost reduction.
- Utilize statistical process control to monitor performance & develop plans to increase robustness & quality control.
- Provide technical support for manufacturing investigations & laboratory experiments.
- Conduct structured problem-solving investigations.
- Document process deviations & assess impact on quality & yield.
- Participate in cross functional teams by handling project management tasks.
- Lead process validation for technology transfers, operational changes, & new technologies.
- Support experimental & validation lot execution, maintaining compliance with current procedures & regulations.
Provide technical support during regulatory audits & submissions & demonstrate accountability for EHS performance.
Education & Experience
Must possess a BS in Chemistry, Biology or Engineering (Chemical, Mechanical, Bio-chemical, or other relevant scientific field) or equivalent education & 5 years of experience as a scientist in the pharmaceutical/medical device/chemical industry.
Of experience required, must have 5 years:
- applying fundamentals of pharmaceutical drug product process including sterile/aseptic product manufacturing, media fill, sterilization, fill finish operations, & cGMP;
- performing design control, process validation, & technology transfer;
- providing regulatory support for IND and BLA submission;
- performing statistical analysis using Minitab, JMP, Lean Six Sigma);
- experience in project management working in a cross functional organization; &
- preparing scientific documents & reports, orally & in writing, for peers, business stakeholders, management & vendors.
Alternatively, would accept, MS or equivalent education Chemistry, Biology or Engineering (Chemical, Mechanical, Bio-chemical, or other relevant scientific field), & 1 year of experience as a scientist in the pharmaceutical/medical device/chemical industry.
Of experience required, must have 1 year of each of (i), (ii), (iii), (iv), (v), (vi) & (vii).
Work experience may be gained concurrently. Will accept reasonable combination of education, training & work experience.
Salary Range: $115,000.00 - $157,500.00 per year.
Apply online at https://careers.abbvie.com/en or send resume to Job.opportunity.abbvie@abbvie.com. Refer to Req ID: REF49711S
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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.
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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