Date Posted: 09/29/2026
Hiring Organization: Rose International
Position Number: 508361
Industry: Biotech/Healthcare
Job Title: Process Development Scientist
Job Location: Foster City, CA, USA, 94404
Work Model: Onsite
Shift: 8 am - 5 pm (Mon - Fri)
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 13
Min Hourly Rate($): 68.00
Max Hourly Rate($): 73.00
Must Have Skills/Attributes: Analytical Skills, Chemistry, Pharmaceutical
Experience Desired: Hands-on laboratory experience required (5 yrs); Experience with formulation development (3 yrs); Experience in Drug Product process development (3 yrs)
Required Minimum Education: Master’s Degree
Preferred Education: Ph.D / Doctorate
**C2C is not available**
Job Description
Required Education:
Bachelor’s degree in a relevant scientific discipline with at least 8 years of industrial experience in biologics Chemistry, Manufacturing, and Controls (CMC) development.
Preferred Education:
Ph.D. in Pharmaceutical Science, Chemistry, Biochemistry, Chemical Engineering, or Master of Science (M.S.) degree with at least 6 years of industrial experience.
Qualifications:
· Hands-on laboratory experience required.
· Experience with 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 strongly desired.
· Publications, external presentations, and the desire to innovate through research strongly preferred.
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 continuously grow technical expertise; influence internally and externally through publication, presentations, and industrial collaboration representation.
· Demonstrate understanding of analytical, biophysical characterization, or process development techniques; bring new capabilities; lead by example for lab executions.
· Fully embrace data integrity and good documentation practices for data and report generation; critically review internal and external documentation.
· Authors technical documents such as protocols, reports, regulatory dossier, etc for internal and external audience.
· Effectively collaborates with both internal and external stakeholders in project meetings.
· Support and contribute to department initiatives or cross-functional projects to drive business process excellence and scientific innovation.
Description:
The Scientist, Biologics Pivotal Formulation and Process Development role is part of the collaborative and interdisciplinary CMC development team aiming to use state-of-the-art technologies and innovative methodologies to advance medicines into the clinic. The success candidate is expected to bring relevant technical expertise, contribute to key functional strategies, and spearhead innovations related to formulation and DP process development. S/he will have growth opportunities through acquisition of new skills, experiences, and professional relationships in a fast-paced and resource-rich environment.
Client Core Values
· Integrity (Doing What’s Right)
· Inclusion (Encouraging Diversity)
· Teamwork (Working Together)
· Excellence (Being Your Best)
· Accountability (Taking Personal Responsibility) - **Only those lawfully authorized to work in the designated country associated with the position will be considered.**
- **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**
Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.
California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.
Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.
If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.
Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).
Rose International has been great to me. I thank everyone there for all of their hard work; it has not gone unnoticed.
Melody, Consultant
Rose International maintained good communication during assignments and are very informative through email and phone calls.
Sade, Consultant
Rose International was not only attentive and responsive, but they were very professional and helpful whenever I called or needed any assistance.
Diane, Consultant
Thanks for the opportunity. If in the future I ever need a job, I would like to work for Rose International.
David, Consultant
Any time I did have a question and called, the phone was always answered, and my question/concern was immediately resolved.
Sally, Consultant
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