Scientist, II PDS&T (24 month Contract) Full-time

AbbVie Job Opportunity

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 including immunology, oncology and neuroscience – and products and services in our Allergan Aesthetics portfolio.

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.

Qualifications

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.

Additional Information

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

Recruitment Fraud Alert

We have recently become aware of various recruitment phishing scams targeting job seekers. Please be advised:

• AbbVie will never request sensitive personal information (such as bank account details, social security numbers, or payment of any kind) during the recruitment process.
• If you suspect you have received a fraudulent offer or communication claiming to be from AbbVie, please do not respond, open any attachments, or click on any hyperlinks.

If you have any questions or concerns regarding the authenticity of a communication alleged to have been made by or on behalf of AbbVie, please contact us immediately.

Protect yourself by verifying job offers and communications. Your safety is important to us.

Where We Work

Role is exclusively performed at a site or office and onsite presence is required. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role.