Sr. Analytical Scientist

Two95 International Inc.; Durham (NC); On-site; USD 120,000 - 180,000; Full time

Job summary

Two95 International Inc. seeks a Senior Analytical Scientist in Research Triangle Park, NC for a 12+ month engagement. The role focuses on analytical development, data interpretation, and transferring methods to CDMOs.

Responsibilities include method development, validation, and analytical testing of solid oral dosage forms using HPLC, FTIR, XRD, SEM, DSC, TGA, and dissolution techniques. Requires BS/MS with extensive pharma analytics or PhD with significant experience.

Qualifications

• BS/MS with 10-12+ years of pharma analytical experience in development/validation.
• PhD with 5-7+ years in analytical development for solid oral dosage forms.
• Excellent method development and validation skills for pharmaceutical materials.
• Experience with multiple analytical techniques/instrumentation (HPLC, FTIR, XRD, SEM, DSC, TGA) preferred.
• Background in contract analytical labs or pharma outsourcing to CDMOs is a plus.

Responsibilities

• Plan and conduct analytical tests for drug development and transfer the methods to CDMO.
• Analyze and interpret data and prepare technical reports.
• Perform IQ/OQ/PQ and maintain lab equipment.
• Follow safety procedures and good laboratory practice.
• Ability to work independently and multi-task to meet timelines.

Skills

Analytical method development

Validation experience

HPLC

Powder XRD

DSC

TGA

FTIR

SEM

Dissolution testing

Data interpretation

Education

BS/MS in Pharmacy/Chemistry related field

PhD in analytical chemistry/pharma

Tools

Agilent HPLC

TGA

DSC

FTIR

Powder XRD

SEM

Dissolution tester

Job description

Title: Sr. Analytical Scientist Location: Research Triangle Park, NC Duration: 12+ months Rate: $Open/hr. Requirements

General Responsibilities:

• Plan and conduct analytical tests for drug development and transfer the methods to CDMO


• Analyze and interpret data and prepare technical reports


• Perform IQ/OQ/PQ and maintain lab equipment


• Follow safety procedures and good laboratory practice


• Must be able to work independently with limited guidance from external consultants or CEO (this role would report directly into the CEO).


• BS/MS with 10-12+ years of pharma industry analytical experience working within analytical development/validation to support solid oral dosage forms (small molecules), Ph.D. with 5-7+ years.


• Excellent method development and validation skills and routine analysis on pharmaceutical materials (including potent compounds).


• Strong preference for an analytical scientist who has used a variety of analytical techniques/instrumentation ? for example, particle size analysis, TGA, DSC, HPLC, FTIR, Powder XRD, SEM, HPLC (Agilent), Dissolution, UV-Vis.


• Strong preference for an analytical scientist who either has worked within a contract analytical lab working with external clients or has worked within a pharma company who outsourced some analytical work to external CDMOs.


• Ability to self-manage and take on new tasks


• Ability to learn new analytical techniques by hands-on work and review of published data


• Ability to multi-task and hit project timelines.


• Excellent oral and written communication skills


• ANDA background a plus.

Benefits