Scientist LCMS (must have industry LCMS experience) ( {{city}})
Solid experience in a few of the area's listed below is needed to succeed in this role:
- LCMS
- Bioanalysis
- Small molecule and/ or large molecule
- Oligonucleotides
- Protein peptides- quantitative experience
- 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
- 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
- Able to document clearly
- Knowledge of and experience in a regulatory environment
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