Research Scientist (Sample Analysis) - Bioanalytical Dept

Mary Dickson; Newark (DE); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Bonuses and merit increases

401(k) plan

Group Life/AD&D Insurance

Short & Long-term Disability Insurance

Park-like setting

Job summary

QPS, LLC is seeking a Research Scientist in the Bioanalytical (GBA) department to advance LC-MS/MS bioanalytical capabilities for drug development programs. You will independently manage studies, design and review protocols, and coordinate with clients and internal teams to deliver high-quality data.

The role requires a Ph.D. in a related field and direct LC-MS/MS experience; CRO background is valued for seniority.

Qualifications

• Advanced degree in Analytical Chemistry, Biochemistry, Pharmacology, or related discipline (Ph.D. required).
• Direct LC-MS/MS experience for bioanalytical assays.
• If >2 years since graduation, experience with method development of bioanalytical LC-MS/MS assays; CRO experience preferred.

Responsibilities

• Manage multiple sample analysis projects with minimal supervision.
• Prepare and review study protocols; coordinate with clients and internal resources.
• Set up and maintain LC/MS instrumentation; ensure GLP compliance and SOP adherence.
• Train and mentor junior scientific staff; report study findings and summaries.

Skills

LC-MS/MS analysis

Experimental design

Data analysis software

Education

Ph.D. in Analytical Chemistry/Biochemistry/Pharmacology

Tools

LC-MS/MS instruments

Job description

Job Description

Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! QPS, LLC has an opening for a Research Scientist in our Bioanalytical (GBA) department. GBA is comprised of three laboratory operation unit: Small Molecules, Proteins, and Oligonucleotides, and each unit has their own Method Development/Method Validation/Sample Analysis (MD/MV/SA) group. In this role, you will play a pivotal part in QPS’ continued expansion of our bioanalytical capabilities to support drug development of small molecules, antibody drug conjugate, protein, and genetic medicines.The GBA department expertise lies in the quantitation of small molecules, peptides, proteins, oligonucleotides, and biomarkers by various chromatographic (standard flow LC, microflow LC, SFC) couple to tandem mass spectrometric (MS/MS, MS/HRMS, hybrid/immunocapture mass spec) techniques. We have been pivotal in supporting most of the HIV drugs, most of the HBV/HCV drugs, 2 of the 15 ADCs, and 7 of the 24 oligonucleotides therapeutics approved by FDA/EMA.

The Job

• Independently manage multiple sample analysis projects/studies at the same time with minimum supervision.
• Prepare, and/or review and understand study protocols.
• Coordinate with client and internal resources to plan, design and conduct studies.
• Evaluate significance of data and report findings.
• Prepare Study summaries and/or reports.
• Set-up, utilize, and maintain complex instrumentation.
• Communicate project timelines, status, data, reports, and inquiries to client and/or study sites, effectively addressing any issues that may arise.
• Maintain the proper level of regulatory compliance for each study, preparing QA related documents and addressing QA audit findings.
• Maintain schedule of projects and timelines.
• Supervise, train and/or mentor junior scientific staff.
• Develop, validate and run sensitive, reliable and efficient LC/MS/MS assays for TK/PK assessment.
• Ensure that GLP regulations and SOPs are followed in all bioanalytical service activities.

Requirements

• The successful candidate will hold an advanced degree in Analytical Chemistry, Biochemistry, Pharmacology, or related scientific discipline: Ph.D. degree.
• Recent graduates must have with direct experience on LC-MS/MS analysis.
• If more than 2 years since graduation, candidates must have direct experience on method development of bioanalytical assays using LC-MS/MS, particularly having CRO experience.
• Understanding of experimental design and planning, and data collection and analysis software.

Work Location

Work LocationThis job will be 100% QPS-office/facility based

Why You Should Apply

• Great learning opportunities, especially for those new to the field.
• Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.
• Structured Career Ladders that provide excellent growth based on your personal aspirations.
• Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.
• Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance.
• Park-like setting in Newark, Delaware.
• Internal committees designed with the needs and enjoyment of QPS employees in mind.

QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.