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.
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Job Description We are now hiring a Senior Scientist to join the Product Development, Science and Technology (PDS&T) team based in Dublin.
The PDS&T team is the intersection of technical excellence and business impact.
We are champions of product innovation and process solve AbbVie's most complex technical challenges to successfully commercialize our pipeline and maintain uninterrupted supply for our patients.
The Small Molecule Drug Product department within PDS&T applies an understanding of pharmaceutical sciences, oral dosage process engineering, and applied statistics when contributing to NPI commercialization activities and product on-market support.
Demonstrate skill in multiple laboratory, equipment and statistical techniques and appropriately modify protocols, as required, to suit the changing needs of research or development sciences.Generate and analyze data from laboratory, pilot, and commercial plant trials and draw relevant conclusions.Analyze and critique results, noting significant deviations.Demonstrate ownership and understanding for all technical aspects of assigned Product(s) including manufacturing, packaging, regulatory, safety, and supply chain.Lead collaborative technical discussions and author/verify/review supporting technical documents.Contribute to Chemistry Manufacturing Controls (CMC) team discussions for strategy, technical assessment/recommendation and data interpretation, timeline, resource, updates, issues, etc.Gain stakeholder buy-in for Drug Product technical strategies.Demonstrate technical proficiency in his/her field.Perform routine tasks competently and independently, generating reliable and consistent results.Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable. Qualifications Bachelor's Degree or equivalent education and typically 12 years of experience, Master's Degree or equivalent education and typically 10 years of experience, PhD and typically 4 years of experience.Possess thorough theoretical and practical understanding of own scientific discipline.Possess ability to work largely independently with limited supervision.Possess ability to work closely with a cross-functional team as required e.g.
Quality, Regulatory, Analytical, Manufacturing Sites, TPMs, Brand Management, Supply Chain.Effective writer and communicator of research or other regulatory materials.Previous work experience in the pharmaceutical or related industry. Additional Information AbbVie is an equal opportunity employer and 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.
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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