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Senior Engineer, CTTO Vector Lab Seattle Dexter - WA - US R1602494

Job in Seattle, King County, Washington, 98127, USA
Listing for: Bristol-Myers Squibb
Full Time position
Listed on 2026-05-24
Job specializations:
  • Engineering
    Process Engineer, Quality Engineering, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 124190 - 150483 USD Yearly USD 124190.00 150483.00 YEAR
Job Description & How to Apply Below
Position: Senior Engineer, CTTO Vector Lab Seattle 400 Dexter - WA - US + 1 more R1602494
## Senior Engineer, CTTO Vector Lab Seattle 400 Dexter - WA - USFind out how well you match with this job
** Working with Us
** Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it.

You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more:  Senior Process Engineer in Cell Therapy Technical Operations (CTTO) will play a key role in ensuring successful manufacture of life-saving cell therapy products.

The primary focus of the Senior Process Engineer will be to support testing and implementation of operational improvements and resolve manufacturing process investigations at the BMS cell therapy GMP manufacturing facilities. This individual will be expected to lead, design and execute experiments, evaluate data, and draft technical reports in support of improvements, investigations, and manufacturing process changes. The Process Engineer will also contribute to well controlled comparability and validation studies which enable regulatory filings for raw material and process changes.

Additionally, this role may lead a group of engineers and provide leadership and technical guidance. The Process Engineer will also partner with cross functional groups and function as Subject Matter Expert (SME) on processes, equipment, and compliance issues in manufacturing.
** Responsibilities:
*** Lead, manage, design, execute, and support experiments in the CTTO DP & Vector labs which includes aseptic processing and operation of automated process equipment.
* Partner with cross functional groups and teams and lead technical projects and discussions.
* Manage and oversee junior engineers on performance, studies, and review technical reports and investigations.
* Summarize experimental data and aid in analysis to draw conclusions.
* Lead or participate in Root Cause Analyses (RCA) to determine cause of manufacturing process investigations.
* Coordinate with the analytical group for timely delivery of process samples and turn-around of analytical data.
* Lead or Support production related investigations, ensuring compliance with internal standards and regulatory requirements.
* Lead, develop, and execute manufacturing process changes and improvement activities, and/or author technical reports for process changes and improvements.
* Lead or support process characterization, process comparability and process validation studies including planning, execution, and documentation management. Support necessary technical experiments and analysis to enable decisions related to raw materials changes.
* Contributes to ownership and advancement of work processes, and procedures.
* Work flexibility with occasional cell cultures experiments on weekends and evenings.
*
* Required Qualifications:

*** Degree in Biological Sciences, Chemical Engineering, Life Sciences, or related discipline.
* BS degree with minimum of 7+ years of relevant experience, or MS degree with minimum 4+ years of relevant experience in biologic process/analytical development or commercial biologic manufacturing process support.
* Excellent documentation skills and diligence with cGMP experience a plus.
* Ability to effectively lead and work in cross functional teams, meet deadlines, and prioritize responsibilities.
* Experience working in a self-driven, performance/results oriented, fast paced matrix environment.
* Excellent critical thinking skills.
* Able to creatively manage time and elevate relevant issues to project lead and line…
Position Requirements
10+ Years work experience
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