About this role
This is an exciting opportunity to work in a collaborative, science-driven environment where you'll have ownership of projects, solve complex technical challenges, and contribute to delivering high-quality medicines that make a difference to patients worldwide.
What You'll Do
As part of our team, you will:
- Design, plan, and execute laboratory studies to support formulation development, process optimization, scale-up activities, and technology transfers.
- Perform and support parenteral drug product activities including compounding, filtration, and filling operations.
- Analyze and interpret scientific data, identify trends, troubleshoot issues, and make data-driven recommendations.
- Author and review technical documents, protocols, reports, procedures, and batch records.
- Support laboratory start-up activities, equipment qualification, and facility readiness in collaboration with engineering, quality, and manufacturing teams.
- Work with internal stakeholders and external vendors to evaluate and improve equipment, systems, and technologies.
- Lead or contribute to investigations, risk assessments, change controls, and problem-solving initiatives.
- Ensure compliance with GMP, quality, data integrity, and safety requirements.
- Drive continuous improvement, digitalization, and knowledge-sharing initiatives across the team.
Education
You will hold a Bachelor's, Master's, or PhD in:
- Pharmaceutical Science
- Biotechnology
- Chemical or Process Engineering
- Drug Discovery & Development
- Or another relevant scientific or engineering discipline
Experience
You will have experience in a pharmaceutical, biotechnology, medical device, technical operations, manufacturing, or regulated laboratory environment.
Level will be determined based on experience:
- Bachelor's Degree: typically 5-7+ years' relevant experience
- Master's Degree: typically 3-5+ years' relevant experience
- PhD: typically 1-2+ years' relevant experience
You'll also bring
- Experience planning and executing scientific experiments independently.
- Strong analytical and problem-solving skills with the ability to interpret complex data.
- Knowledge of GMP/GxP requirements, quality systems, validation concepts, and data integrity principles.
- Experience with sterile manufacturing, aseptic processing, filtration, formulation development, lyophilization, or related parenteral technologies would be an advantage.
- A proven ability to collaborate effectively within cross-functional project teams.
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