Scientist, II PDS&T (24 month Contract)

This is an exciting opportunity to work in a collaborative science-driven environment where youll have ownership of projects solve complex technical challenges and contribute to delivering high-quality medicines that make a difference to patients worldwide.

What Youll 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 Bachelors Masters 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:

• Bachelors Degree: typically 5-7 years relevant experience
• Masters Degree: typically 3-5 years relevant experience
• PhD: typically 1-2 years relevant experience

Youll 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  & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

No

Employment Type :

Full-time