Senior Scientist l, Drug Product Manufacturing

Career Opportunities: Scientist II, Drug Product Manufacturing (5534)

Requisition ID 5534 - Posted 06/29/2026 - Cranbury, NJ - United States

Job Title - Scientist ll, Drug Product Development

Work Location - Cranbury NJ

Job Summary

Drug product process development (DPD) is seeking a scientist to join our department. The successful candidate will be expected to work as part of a ream that is focused on the activities including but not limiting to formulation development, drug product manufacturing process development and technical transfer, clinical in use compatibility study, and drug product manufacturing support. Work closely with analytical sciences (AS) and process development and drug product manufacturing teams to lead formulation development projects. Responsible for study design, execution and trouble-shooting to meet client project deliverables. Author technical documents including SOPs, protocols, study reports, etc

Responsibilities

• Understanding of the drug product manufacturing processes and scaling up.
• Understanding of the liquid formulation development and fill/finish process scale up.
• Develop formulation for biologics to support stability including study planning, design, execution and author study report to manage the DPD project life cycle.
• Develop injectable drug product manufacturing process including container closure selection, drug product compatibility with manufacturing process, and provide tech transfer and manufacturing support including deviation investigation and trouble shooting
• Author technical documents including SOPs, protocols, study reports, and support regulatory filing.
• Play an important role in Formulation/DPD lab startup efforts including Lab design, equipment selection/procurement, authoring documentation and support the team building activities.
• Apply scientific knowledge and experience to assigned projects. Interface extensively in a matrixed environment with process development, analytical development and manufacturing teams for process investigation support, assess new formulation/DPD technologies, support on-going and upcoming client projects.
• Communicate effectively on the findings of research and development internally and externally to ensure alignment among WuXi Biologics and with clients

Preferred:

• Drug product process development experience with large molecules for parenteral administration
• Development and characterization of aseptic fill and finish operations including freeze/thaw, compounding, mixing, sterile filtration, filling, stoppering, visual inspection,
• Manufacturing experience of biologics drug product in clinical settings
• Experience in biophysical characterization of the biologics drug products

Qualifications

• PhD in Pharmaceutics, Pharmaceutical Sciences, Pharmaceutical Chemistry or Chemistry

Candidate must possess knowledge in formulation, high concentration protein formulation, matching placebo development, and drug product process development areas. Understand current industry practice and scientific reasoning for biologics product formulation development.

• Strong communications skills. Great team player and ability to build positive collaboration with internal stakeholders, vendors and clients to achieve alignment and work effectively.
• Must work in a self-motivated, multiple tasks, highly flexible, well-organized and detailed-oriented style.
• May require some evening work hours and conference call time to meet global team time zones..
• The job description does not intend to list all the duties and responsibilities assigned to this position. Employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and company business needs.

The Anticipated salary for this position is $73,000 - $117,000

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability

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