Scientist - Process Development - IV

VARITE • Foster City, CA

3d • Onsite

About The Position

The Scientist, Biologics Pivotal Formulation and Process Development role is part of a collaborative, interdisciplinary CMC development team using state-of-the-art technologies and innovative methods to advance medicines into the clinic. The successful candidate will contribute relevant technical expertise, help shape functional strategies, and lead innovation in formulation and drug product process development. The role offers opportunities to develop new skills, experiences, and professional relationships in a fast-paced, resource-rich environment.

This is an onsite, 12-month contract position in Foster City, California, with a possible extension. The stated pay range is $60.00 to $63.30 per hour on W-2.

Requirements

• Ph.D. in Pharmaceutical Science, Chemistry, Biochemistry, Chemical Engineering, or a related scientific field, with 0 or more years of industrial experience in biologics CMC development; or an M.S. with 6 or more years; or a B.S. with 8 or more years.
• Hands-on laboratory experience.

Nice To Haves

• Experience in formulation development, drug product process development, and clinical in-use evaluation for monoclonal antibodies, bispecifics, antibody-drug conjugates, fusion proteins, and other complex biologics formats.
• Publications, external presentations, and a desire to innovate through research.

Responsibilities

• Design and execute formulation and drug product process development work packages, including formulation development, drug product manufacturing process development, and clinical in-use evaluations.
• Drive innovation and develop technical expertise; influence internal and external audiences through publications, presentations, and representation in industrial collaborations.
• Demonstrate understanding of analytical, biophysical characterization, or process development techniques; bring new capabilities and lead by example in laboratory execution.
• Follow data integrity and good documentation practices in data and report generation, and critically review internal and external documentation.
• Author technical documents, including protocols, reports, and regulatory dossiers, for internal and external audiences.
• Collaborate effectively with internal and external stakeholders in project meetings.
• Support and contribute to department initiatives and cross-functional projects that advance business process excellence and scientific innovation.

Benefits

• Medical, dental, and vision coverage.
• Participation in a company-sponsored retirement savings plan.
• Legal service plans providing access to attorneys for advice and representation.
• Eligible employees may be eligible for an employee referral bonus.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level