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Sr Scientist
Date: Aug 1, 2025
Location:West Chester, United States, Pennsylvania, 19380
Company: Teva Pharmaceuticals
Job Id: 63185

WHO WE ARE

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

YOUR EXPERIENCE AND QUALIFICATIONS

Required Qualifications:

• Ph.D. in pharmaceutical sciences, biochemistry, chemical engineering, or related field with 5+ years of experience; MS with 7+ years; or BS with 10+ years relevant experience
• Biologic drug product development expertise
• Experience developing drug product manufacturing processes, including aseptic processing training
• Skilled in DP process risk assessment and characterization
• Experienced in working within cross-functional teams, with ability to build cross-departmental relationships
• Knowledge of CMC requirements for regulatory submissions (INDs, BLAs) and experience writing DP sections

Preferred Qualifications:

• Experience working with manufacturing sites, external service partners and CMOs
• Familiar with single-use manufacturing technologies
• Experience with application of Quality by Design (QbD) to drug product development
• Strong organizational skills and attentive to detail
• Excellent written and oral communication skills

• Responsible for developing drug product manufacturing processes
• Design and implement process characterization
• Author protocols, development reports, risk assessments, and other technical documentation
• Facilitate and support technology transfer to pilot manufacturing sites for clinical supply production
• Lead cross-functional team to manage tech transfer to commercial sites
• Represent DPD on cross-functional matrix teams pertaining to biosimilar and novel biologic products at Teva
• Coordinate, support, and liaise with GMP manufacturing facilities and / or external contract organizations regarding the production of non-clinical and clinical drug product batches
• Provide technical expertise for resolving issues related to drug product processing technologies and equipment
• Serve as a subject matter expert, supporting manufacturing operations through technical evaluation of change controls, deviations, and implementation of corrective and preventive action