Post Doctorate Scientist

Qps-Holdings,-LL; Newark (DE); On-site; USD 70,000 - 80,000; Full time

Job summary

QPS, LLC in Newark, Delaware is seeking a Post Doctorate Scientist to advance method development and validation, and to develop LC-MS/MS assays for TK/PK/Biomarker assessment in a GLP-compliant environment. This is a two-year, temporary position with potential for permanency and growth.

The role supports four lab units within Bioanalytical (GBA) and involves working across projects while maintaining quality and accuracy in analyses performed.

Qualifications

• Ph.D. in Analytical Chemistry, Biochemistry, Microbiology, Pharmacology, Food Science, Plant Science or related discipline with hands-on mass spectrometry.

Responsibilities

• Independently manage one or more method development/validation studies with minimal supervision.
• Prepare, and/or review study protocols and evaluate data significance.
• Prepare study summaries/reports and maintain regulatory compliance for each study.

Skills

Mass spectrometry

LC-MS/MS

Method development/validation

GLP compliance

Data interpretation

Education

Ph.D. in Analytical Chemistry or related discipline

Tools

LC-MS/MS instrumentation

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Post Doctorate Scientist

Full Time Regular Mid-Level Prof-Lab Newark, DE, US

3 days ago Requisition ID: 3241

Salary Range: $70,000.00 To $80,000.00 Annually

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 two Post Doctorate in our Bioanalytical (GBA) department. GBA is comprised of four laboratory operation units: Small Molecules, Oligonucleotides, Proteins, and Support Functions. This is a two-year temporary position with the potential for a permanent position. In this role, you will play a pivotal part in QPS’ continued expansion of our bioanalytical capabilities to support biomarker quantitation.

Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.

Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.

The Job

• Independently manage one or more method development/validation studies at the same time with minimum supervision.
• Prepare, and/or review and understand study protocols.
• Evaluate the significance of data and report findings.
• Prepare Study summaries and/or reports.
• Set-up, utilize, and maintain complex instrumentation
• 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.
• Develop, validate and run sensitive, reliable and efficient LC-(HR)MS/MS assays for TK/PK/Biomarker assessment.
• Ensure that GLP regulations and SOPs are followed in all bioanalytical service activities.

Work Location

• This job will be 100% QPS-office/facility based

Requirements

• Ph.D. in Analytical Chemistry, Biochemistry, Microbiology, Pharmacology, Food Science, Plant Science or related scientific discipline with hands-on experience in mass spectrometry.

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.