Post Doctorate Scientist

QPS Holdings, LLC; Newark (DE); On-site; USD 80,000 - 90,000; Full time

Job summary

QPS, LLC in Newark, Delaware, seeks a Post Doctorate Scientist for its Bioanalytical (GBA) department. This full-time, two-year temporary role focuses on developing and validating LC-MS/MS assays for TK/PK/biomarker assessment under GLP conditions.

The successful candidate will independently manage method development, review study protocols, evaluate data, and prepare study summaries while maintaining regulatory compliance and project timelines.

Qualifications

• Ph.D. required with hands-on MS experience.
• Experience with method development and validation.
• Knowledge of GLP regulations and bioanalytical workflows.

Responsibilities

• Independently manage method development/validation studies.
• Prepare and review study protocols and reports.
• Evaluate data and report findings.
• Set up, maintain LC–MS/MS instrumentation and workflows.
• Ensure regulatory compliance and QA documentation.
• Maintain project timelines and study schedules.
• Develop and run TK/PK/biomarker LC–MS/MS assays.
• Follow GLP SOPs in all activities.

Skills

Mass spectrometry

LC-MS/MS

Regulatory familiarity

Education

Ph.D. in Analytical Chemistry or related

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

29 days ago Requisition ID: 3241

Salary Range: $80,000.00 To $90,000.00 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.