Resolian
Scientist I LCMS (must have industry LCMS experience)
Resolian, Malvern, Pennsylvania, United States, 19355
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
The full job description covers all associated skills, previous experience, and any qualifications that applicants are expected to have.
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
The full job description covers all associated skills, previous experience, and any qualifications that applicants are expected to have.
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