Genesis Drug Discovery and Development (GD3), a member of the Genesis Biotechnology Group is a fully integrated contract research organization providing services to support preclinical drug discovery programs from early discovery through preclinical development. The Company’s diversified portfolio of services covers all areas of preclinical drug discovery/development including Discovery Biology, Medicinal Chemistry, DMPK/in-vivo pharmacology, and GLP Toxicology.

GD3 is seeking experienced bioanalytical scientists to support pharmacokinetic work. The candidate will development and execute a wide variety of small molecule (and potentially large molecule) assays that support early discovery, development and/or clinical sample analysis. We are looking for self-motivated individuals who values working in a team-oriented environment and directly contributing to projects within a close-knit and dynamic setting that focuses on productivity, teamwork, and efficiency.

Primary Responsibilities:

• Serve as Project Manager, Principal Investigator, or Study Director for client projects
• Develop bioanalytical and analytical methods based on LC-MS/MS, HPLC-UV, and ELISA techniques
• Qualify and validate bioanalytical and analytical test methods
• Effectively summarize results for management and clients
• Act as technical expert and trainer for GLP/cGMP laboratory operations
• Prepare validation protocols, test methods, and reports for non-GLP and GLP purposes, the latter in accordance with GLP and cGMP regulations
• Supervise laboratory OOS investigations
• Perform technical and Quality Control (QC) review of laboratory data and reports
• Prepare, review, and approve SOPs
• Experience in PK study design, data interpretation, and analysis

Qualifications:

• Ph.D. in Analytical Chemistry Biochemistry, Pharmacology, or related scientific discipline.
• Experience developing and executing LC-MS/MS and/or HPLC methods/assays
• Experience performing bioanalytical and/or analytical method validation
• Method development
• Experience and/or desire working in a GLP-regulated laboratory setting highly preferred
• Experience in various ADME/DMPK relevant areas such as physicochemical properties, pharmacokinetics, and bioanalytical sciences
• Experience in PK/PD concepts
• Ability to work independently as well as within collaborative team environments.
• Strong written and computer skills.

Thanks & Regards

Mustafa +1 609 808 3923

Job Types: Full-time, Part-time

Salary: $1.00 - $2.00 per year

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Life insurance
• Paid time off
• Vision insurance

Schedule:

• 10 hour shift
• 8 hour shift

Ability to commute/relocate:

• Township of Hamilton, NJ 08690: Reliably commute or planning to relocate before starting work (Required)

Experience:

• Laboratory experience: 1 year (Preferred)

Work Location: One location

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