Scientist, Analytical Development - New Brunswick, United States - Bristol-Myers Squibb

Bristol-Myers Squibb
Bristol-Myers Squibb
Verified Company
New Brunswick, United States

3 weeks ago

Mark Lane

Posted by:

Mark Lane

beBee recruiter
Description

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 rich in diversity.

Take your career farther than you thought possible.


Drug Product Development (DPD)


Our Drug Product Development team is committed to CMC design, development, and commercialization of innovative drug products to improve patient lives.

We leverage the best people, collaboration, and cutting-edge innovation to achieve this commitment.

BMS's internal engine of innovation includes unrivaled industry leading expertise in CMC development of small molecules, protein biotherapeutics, protein degraders, and other therapeutic modalities.

We collaborate closely with our colleagues in R&D and Commercial to design our drug products. Here, you'll get the chance to grow and thrive through opportunities that are uncommon in scale and scope.


Position Summary

Key Responsibilities

  • Develop fitforpurpose analytical methods (e.g., electrophoretic
- and/or chromatography-based) to support sterile drug product development.

  • Conduct characterization, investigation, and troubleshooting to provide key insights and understanding for drug product CQA assessment.
  • Independently analyze, review and document analytical data in compliance with regulatory requirements and generate timely and concise documentation of scientific results.
  • Work with multidisciplinary teams to resolve challenges encountered in drug development through experimental design and execution.
  • Champion lab safety and lab organization.

Qualifications & Experience

Required:


  • Indepth knowledge of analytical chemistry, with handson experience in chromatography techniques (HPLC, UPLC, 2DLC) or electrophoretic techniques (CE-SDS, CZE, icIEF) for protein and nucleic acid analyses.
  • Experience working with other analytical techniques such as LC/MS, SEC, Spectroscopy or light scattering techniques.
  • Strong fundamental knowledge of protein/DNA/RNA structure and function.
  • Ability to execute and document scientific experiments and effectively communicate study results.
  • Demonstrated problem solving skills and strong desire to grow scientifically.
  • The ability to collaborate and work effectively with individuals and as part of crossfunctional teams.
  • Strong written and oral communication skills.


Experience performing quantitative analysis as well as the analysis of nanoparticle, liposome, long acting injectable, and other novel sterile product drug delivery technologies.


Other Qualifications:


PhD (0-2 years industry or post-doc experience) or a MS degree with demonstrated industry experience (2-4 years) or BS degree with demonstrated industry experience (5-7years) in analytical chemistry or related fields.


Development Value:

The Scientist will have interdepartmental responsibilities with regards to participating in workgroups, cross-functional teams, implementation/execution, and cultural initiatives.


Uniquely Interesting Work, Life-changing Careers

On-site Protocol
BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs.

The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility.

For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture.

For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities.

As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
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