Bristol Myers Squibb
Assistant/Associate Scientist
Skills
25 days ago
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Important information
Contract type:
Freelance / Contract
Location:
Seattle, WA, USA
Work mode:
Onsite
Published on:
30 September 2026
What they need
- The Assistant/Associate Scientist/Engineer to join our Vector and Gene Delivery MS&T group in GDPAD. The successful candidate will design and execute experiments related to supporting commercial vector manufacturing processes. This person will collaborate across all CMC functional areas to insure project advancement, rapid and best in class execution, and communication of challenges/opportunities.
Duties/Responsibilities
- Oversee lab activities and schedule
- Design studies to support commercial manufacturing deviation investigations.
- Support the the execution of process characterization studies.
- Collaborate with commercial vector team to identify opportunities for process improvements, make formal recommendations.
- Lead identification and implementation of new technologies and procedures from Development into Manufacturing
- Lead efforts focusing on alignment and harmonization of manufacturing process across multiple sites
- Support the hands-on training of commercial process unit operations to Vector MS&T
- Identify, design and manage small capital engineering projects
Top Skills
- The candidate must have demonstrated verbal, written, and communication skills including ability to present complex information clearly and concisely, with a successful proven history of working with technical teams.
- Experience should include management of lab activities, technical support of a cGMP manufacturing facility, including strong knowledge and engineering leadership for viral vector manufacturing and processing equipment, and process characterization.
- Prefer experience with leading experiments and designing DOEs
- Prior experience in/knowledge of cell culture, viral vector manufacturing, recovery and/or purification of viral vector product in a manufacturing environment preferred
Qualifications
- Specific Knowledge, Skills, Abilities, etc:
- The candidate must have demonstrated verbal, written, and communication skills including ability to present complex information clearly and concisely, with a successful proven history of working with technical teams.
- Experience should include management of lab activities, technical support of a cGMP manufacturing facility, including strong knowledge and engineering leadership for viral vector manufacturing and processing equipment, and process characterization.
- Prefer experience with leading experiments and designing DOEs
- Prior experience in/knowledge of cell culture, viral vector manufacturing, recovery and/or purification of viral vector product in a manufacturing environment preferred
- Prior experience with SOPs, cGMPs and how they are applied within a regulatory environment required
- Prior experience participating in process characterization preferred
Education/Experience/ Licenses/Certifications
- Degree in Biology, Chemistry, Biochemical or Chemical Engineering, or equivalent area of related experience in biologics upstream manufacturing
- Preference given to candidates with experience performing process characterization
- Knowledge of cellular immunology and/or vector manufacturing a plus
- Experience with cGMP, ICH guidelines, PPQ (process validation), control strategy development, and working within a Quality organization
- Proficiency utilizing MS Office products and working knowledge of statistical software (R, JMP, Minitab)
- Experience working in a self-driven, performance/results oriented, fast paced matrix environment
- Experience writing experimental plans and protocols
- Physical Demands:
- Position requires repetitive use of hands and wrist (computer work), and infrequent lifting of items not to exceed 50 lbs
- Occasional bending, twisting and stooping to allow for gowning into classified environment required
- Work Environment:
- Position will require time in the office and lab
- Position is a team & project-based position that will require occasional shift work, weekends, and holidays
This posting is for a contract assignment with ASK Staffing DBA ASK Consulting to provide services to Bristol Myer-Squibb .
The starting hourly compensation for this assignment is the following range ($45.00 - $50.31/hr). While the final, individual compensation and any available benefits will be determined by your employer of record ASK Staffing, Inc (and not BMS), factors that will be included in making the final determination may include the characteristics of the assignment, such as demonstrated experience, required skill, and the geographic location where the job is performed. The starting hourly compensation may be subject to change.
About ASK Consulting ASK Consulting is an award-winning, woman-owned staffing and recruitment solutions provider with over three decades of industry experience. We specialize in connecting businesses of all sizes?across IT, healthcare, engineering, finance, and more?with top-tier professionals. Backed by a global network and personalized service approach, our team is dedicated to building meaningful partnerships that drive organizational success and empower job seekers to excel in their careers.
Benefits ASK Consulting provides comprehensive, ACA-compliant health coverage, along with dental, vision, Short- and Long-Term disability for eligible employees. We also offer commuter benefits, a 401(k) plan with no matching, and a referral bonus program. In addition, ASK Consulting offers unpaid leave and paid sick leave as required by law.
Equal Opportunity Employer ASK Consulting is an equal opportunity employer and does not discriminate against employees or applicants based on race, religion, color, sex, national origin, age, sexual orientation, gender identity, genetic information, disability, veteran status, or any other classification protected by federal, state, or local laws.
California Applicant Notice ASK Consulting is committed to complying with the California Privacy Rights Act (?CPRA?), effective January 1, 2023, as well as all relevant data privacy laws in the jurisdictions where we recruit and hire. To learn more, please review our Notice to California Job Applicants Regarding the Collection of Personal Information on our website. Applicants with disabilities may request this notice in an alternative format by [email protected].
Fair Chance Employment Notice If you are selected for a position at, ASK Consulting, your offer is contingent upon successfully meeting several requirements, which may include a criminal background check. In accordance with all applicable federal, state, and local ?Fair Chance? ordinances and laws?such as the Los Angeles County Fair Chance Ordinance (FCO) and the California Fair Chance Act (FCA)?we consider qualified applicants with arrest or conviction records. The background check will evaluate whether any criminal history could reasonably pose a direct, negative impact on job-related safety, security, trust, regulatory compliance, or overall suitability for the role. Findings that raise concerns may result in withdrawal of a conditional job offer.
To learn more about how ASK Consulting collects and uses personal information during the recruiting process, please review our Privacy Notice andCCPA Addendum. As part of our recruitment efforts, we may ask you to disclose various categories of personal information, including identifiers, professional details, commercial information, educational background, and other related data. ASK Consulting will use this information solely to facilitate the recruitment process.
This posting does not constitute an offer of employment. All applicants seeking positions in the United States must be legally authorized to work in the United States. Submitting intentionally false or fraudulent information in response to this posting may disqualify you from consideration. Any eventual offer of employment will be considered ?at will,? regardless of the expected assignment duration.
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