LC/MS Applications Scientist – Biocolumns
Company websiteagilent.com (Agilent, opens in new tab)
Base salary $107,440 to $167,875
Employer-published annual base salary, USD. Advertised base range in Wilmington, DE
You apply on the employer's own site. Six Figure Work does not handle applications.
- LocationWilmington, DE
- WorkplaceWorkplace not stated
- Status at last checkSource accepting applications when checked
- Last checked (50 min ago) · observed since
About this job
Job Description
Agilent encourages and supports discoveries that advance the quality of life. We provide life science, diagnostic, and applied market laboratories worldwide with instruments, services, consumables, applications, and expertise. Agilent enables customers to gain the answers and insights they seek—so they can do what they do best: improve the world around us. Want more information on Agilent? Check out https://www.agilent.com!
The Application Scientist will be based at our Little Falls, Delaware facility, developing applications for new products supporting the biopharma market. This role requires an onsite presence four days per week.
As the successful candidate, you will contribute to the development of HPLC workflows designed to enhance HPLC and LC/MS biopharmaceutical sample preparation, method development, and data analysis to enable analysis of peptide, oligonucleotide, and protein (mAb) therapeutics. The candidate will also ensure the success of new products by generating product proof points, competitive comparison data, and workflow methods published as Application Notes.
We are looking for a candidate who brings broad, state-of-the-art knowledge of biopharmaceutical therapeutics development and characterization trends. The successful candidate will have a strong background in assay development, including knowledge of CQAs for GLP-1 peptide, oligonucleotide, and protein therapeutics, and purification analysis via HPLC and LC/MS. She/he will join the Biopharma product management team that develops new products and methodologies and brings them to market. As the Application Scientist, you will design and execute the experiments required to create reproducible and robust workflows, application notes, whitepapers, and posters needed for customers to rapidly adopt these workflows in therapeutic development and QA/QC manufacturing release. The candidate will also serve as a technical expert. This will include, but is not limited to, customer presentations, troubleshooting assistance, and field support.
We foster a collaborative and informal team culture built on trust, respect, and clear accountability. Our work pace is fast, driven by a shared passion for delivering outstanding biopharma solutions. Together, we strive for excellence in serving our customers and ensure we develop professionally while delivering business success.
Key Responsibilities
- She/he will be a member of the Biopharma product marketing team that develops new products and workflow methodologies, brings them to market, and publishes application notes using these workflows.
- As the Application Scientist, you will design and execute experiments required to create reproducible and robust workflows, application notes, whitepapers and posters required for customers to rapidly adopt these workflows in therapeutic development and QA/QC manufacturing release.
- The candidate will also serve as a technical expert. These duties include, but are not limited to, customer presentations, troubleshooting assistance, and field support.
You’ll Work Closely With
- Product Managers across the Biopharma Marketing team and more broadly across Agilent.
- R&D in the development and testing of new products and technologies.
- Manufacturing as a resource for testing process improvements and consulting on technical issues.
- The Commercial team supports customer technical questions.
Qualifications
- Ph. D. degree or equivalent in the field of chemistry, analytical chemistry, biochemistry, or related fields required.
- 4+ years of experience with Biopharmaceutical CQA or purification analysis.
- Prior biopharmaceutical industry experience is a plus.
- Prior experience with GLP-1 therapeutics, peptides, diabetes applications, injectables, or drug-product development is a plus.
- CQA experience, including characterization/testing of Critical Quality Attributes, is highly desired.
- Experience with HPLC, LC/MS instrumentation, software, and sample preparation required.
- Ability to work independently and be self-motivated but also collaborative, contributing to the success of multidisciplinary teams.
- Experience and comfort with technical writing and presentations in English
- Possess strong communication skills and be willing to travel to present at conferences and at customer sites.
Additional Details
This job has a full time weekly schedule. Applications for this job will be accepted until at least October 29, 2026 or until the job is no longer posted.The full-time equivalent pay range for this position is $107,440.00 - $167,875.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locationsAgilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email [email protected] or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.Travel Required:
10% of the TimeShift:
DayDuration:
No End DateJob Function:
MarketingSource: Agilent on Workday · View original posting (opens in new tab)
Pay in context
This role's base floor ($107,440) is above 8% of the 1,811 Science & Research roles nationwide listed on this site; 1 other lists the same floor. Their median floor is $153,000; the middle half runs from $124,714 to $180,615.
Only jobs on this site count, and each one publishes a base salary of $100,000 or more, so this compares six-figure jobs with each other, not with the whole market. Computed Nov 8, 2026.
This listingLC/MS Applications Scientist – Biocolumns$107,440 to $167,875
BCSL Clinical Laboratory Technician$104,774 to $163,710
Quality/Regulatory Supervisor$105,280 to $164,500
Automation Project Engineer$103,200 to $161,250
Process Engineer$103,200 to $161,250
Process Engineer - Advanced$103,200 to $161,250
Senior Electrical Engineer - Manufacturing Systems, Test & Automation$103,200 to $161,250
Chart as a table
| Role | Published base |
|---|---|
| LC/MS Applications Scientist – Biocolumns (this listing) | $107,440 - $167,875 |
| BCSL Clinical Laboratory Technician | $104,774 - $163,710 |
| Quality/Regulatory Supervisor | $105,280 - $164,500 |
| Automation Project Engineer | $103,200 - $161,250 |
| Process Engineer | $103,200 - $161,250 |
| Process Engineer - Advanced | $103,200 - $161,250 |
| Senior Electrical Engineer - Manufacturing Systems, Test & Automation | $103,200 - $161,250 |
Observed changes
- First observed on the employer's board
- Began meeting the published-salary criteria
- Observed since
- Employer-stated posting date
- 2026-10-22
Where this pay comes from
Location as the employer wrote it: US-DE-Wilmington
The full-time equivalent pay range for this position is $107,440.00 - $167,875.00/yr plus eligibility for bonus, stock and benefits. Our pay
- Method
- Employer text, read with fixed rules and re-verified
- Checked
- Rule set
- us-base-v2
The pay passage appears in the employer's own job text. Fixed, deterministic rules located it, and the passage below was checked against the stored copy of the posting.
What we verified
- The pay figures come from the employer's own listing, quoted exactly above.
- The pay is an annual base salary in US dollars with a minimum of at least $100,000.
- The role was publicly listed on the employer's job board when last checked.
We do not verify what the employer will actually offer, whether the employer is still recruiting for the role, or anything beyond what the employer published. Full methodology.
