Cell Therapy Process Development Associate

Bristol Myers Squibb; Seattle (WA); On-site; USD 60,614 - 66,124; Full time

Benefits offered by this job

Health coverage

Dental

Vision

Short-term disability

Long-term disability

Commuter benefits

401(k) plan (no matching)

Referral bonus

Paid sick leave

Unpaid leave

Job summary

Bristol Myers Squibb is seeking an Assistant Scientist to support manufacturing of cell therapy products at a GMP facility. You will test and implement operational improvements, execute experiments, analyze data, and draft technical reports to support process changes and regulatory filings.

You will collaborate with analytical teams and contribute to comparability and validation studies, enabling regulatory submissions.

Qualifications

• Degree in Biological Sciences or related discipline.
• BS with 2+ years or MS with 0+ years in biologic process/analytical development.
• Strong documentation and cGMP experience preferred.
• Able to work in cross-functional teams and meet deadlines.
• Excellent problem-solving and communication skills.

Responsibilities

• Execute experiments in process development labs including aseptic processing and operation of automated process equipment.
• Summarize experimental data and aid in analysis to draw conclusions.
• Coordinate with analytical group for timely delivery of process samples and data.
• Support production-related investigations ensuring compliance with standards and regulatory requirements.
• Develop and execute manufacturing process changes and improvement activities.
• Support process comparability and validation studies including planning, execution, and documentation management.
• Maintain flexibility with schedule for cell cultures on occasional weekends or evenings.

Skills

Technical writing

Problem solving

Communication skills

Team collaboration

Time management

Education

BS in Biological Sciences or related

MS in Biological Sciences or related

Tools

MS Office

R

JMP

Minitab

Job description

Bristol Myers Squibb is seeking an Assistant Scientist to support manufacturing of cell therapy products at a GMP facility. You will test and implement operational improvements, execute experiments, analyze data, and draft technical reports to support process changes and regulatory filings.

You will collaborate with analytical teams and contribute to comparability and validation studies, enabling regulatory submissions.