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Scientist LCMS (protein quantitation)

Resolian

Malvern (Chester County)

On-site

USD 43,000 - 52,000

Full time

15 days ago

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Job summary

An established industry player is expanding its dynamic team of scientists specializing in bioanalytical services. This exciting role involves working with cutting-edge LC-MS technology to conduct method development and validation, ensuring high-quality results in drug metabolism and pharmacokinetics. The ideal candidate will thrive in a collaborative environment, contributing to innovative projects while adhering to regulatory standards. If you're passionate about science and eager to make a significant impact in the biotechnology field, this opportunity is perfect for you.

Qualifications

  • 5 years experience working LCMS at a CRO or pharma/life sciences company.
  • Able to independently perform complex lab work.

Responsibilities

  • Prepare reagents, standards, and control samples.
  • Analyze samples using various techniques specific to department.
  • Lead troubleshooting activities; assays and equipment.

Skills

Protein quantitation
Immunoaffinity procedures
LCMS
Bioanalysis
GxP including GOP & GCP
Method development
Sample analysis using LCMS

Education

BA/BS in relevant field
PhD in relevant field

Tools

Analytical equipment
High resolution mass spec

Job description

2 weeks ago Be among the first 25 applicants

Direct message the job poster from Resolian

Resolian is a Contract Research Organization (CRO) specializing in Drug Metabolism/ Pharmacokinetic (DMPK) and bioanalytical services for both small and large molecules.

Resolian is growing and due to our growth, we are adding Scientists to our Bioanalytical, LC-MS team.

Solid experience in a few of the area's listed below is needed to succeed in this role:

  • Protein quantitation (must have)
  • Immunoaffinity procedures
  • LCMS (must have)
  • Bioanalysis (must have)
  • Small molecule and/ or large molecule
  • GxP including GOP & GCP
  • Method development & sample analysis using LCMS

Responsibilities:

· Prepare reagents, standards, and control samples

· Analyze samples using various techniques specific to department

· Perform complex method development with limited supervision

· Perform method validation or qualification

· Operate analytical equipment

· Lead troubleshooting activities; assays and equipment

· Maintain analytical equipment

· Review, evaluate, and interpret data results

· Draft and present posters/presentations

· Train and mentor lower level Scientists

· Collaborate with clients and vendors

· Ensure lab area is clean and inspection ready at all times

· Remove lab waste

· Record tasks in accordance with Good Documentation Practices (GDP)

· Understand and apply regulatory requirements; GLP, GCP, 21CFR Part 11

· Follow applicable SOPs and procedural documents

· Other tasks as assigned

Qualifications & Education:

  • BA/BS or higher with 5 years experience working LCMS at a CRO or pharma/ life sciences company
  • PhD in relevant field with two years experience working in LCMS at a CRO or pharma/ life sciences company
  • Experience immunoaffinity procedures
  • Familiarity with high resolution mass spec is a plus
  • Knowledge and understanding of regulatory requirements; GLP, GCP, 21CFR Part 11, GDP, GMP
  • Able to independently perform complex lab work
  • Able to work in a regulated environment
  • Able to work effectively and contribute within a team
  • Able to work with computer systems
  • Knowledge of and experience in a regulatory environment
  • Team building experience

More information about the LC-MS group: www.alliancepharmaco.com/services/bioanalytical/

More information about Resolian: www.resolian.com

Seniority level
  • Seniority level
    Associate
Employment type
  • Employment type
    Full-time
Job function
  • Job function
    Science and Research
  • Industries
    Biotechnology Research and Research Services

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