Pharma R&D Scientist: Method Development & GMP Testing

TekWissen ®; Cincinnati (OH); On-site; USD 41,000 - 48,000; Full time

Benefits offered by this job

TekWissen Group is an equal-opportu n:

Job summary

TekWissen is seeking a Research and Development Scientist for a 12‑month, onsite assignment in Cincinnati. The role focuses on analytical testing, method development, and data review to support pharmaceutical development and manufacturing activities within GMP guidelines.

The ideal candidate has 2–3 years of GMP laboratory experience, hands‑on analytical testing skills (HPLC/UPLC, GC, dissolution), and strong communication abilities to deliver high‑quality results under regulatory requirements.

Qualifications

• Bachelor’s degree in Chemistry, Biochemistry, or related field.
• 2–3 years of GMP laboratory and regulatory experience.
• Experience with HPLC/UPLC, GC, and dissolution testing.
• Hands-on pharmaceutical analytical testing experience.
• Familiar with GMP, GLP, SOPs, and safety procedures.
• Strong written and verbal communication skills.

Responsibilities

• Perform routine chemical and physical testing of pharmaceutical finished products and stability samples using chromatographic, spectroscopic, dissolution, and other analytical techniques.
• Develop analytical methods and participate in validation of methods for pharmaceutical raw materials and finished products.
• Write and execute analytical method validation protocols in accordance with regulatory requirements and approved laboratory procedures.
• Process, review, interpret, document, and report analytical data.
• Communicate analytical results clearly to internal teams and external clients and provide data-based recommendations.
• Maintain and troubleshoot analytical instrumentation.
• Support implementation of new analytical methods and laboratory processes.
• Manage assigned project tasks with minimal supervision and ensure deliverables are completed on time.
• Identify and communicate project next steps, issues, and potential solutions.
• Perform all work in compliance with SOPs, GMPs, GLPs, and applicable safety requirements.

Skills

HPLC/UPLC

GCHS

Dissolution testing

Analytical method development

GMP knowledge

GLP knowledge

Data interpretation

Education

Bachelor’s degree in Chemistry or Biochemistry

Tools

Chromatography systems

Spectroscopy instruments

Data analysis software

Job description

TekWissen is seeking a Research and Development Scientist for a 12‑month, onsite assignment in Cincinnati. The role focuses on analytical testing, method development, and data review to support pharmaceutical development and manufacturing activities within GMP guidelines.

The ideal candidate has 2–3 years of GMP laboratory experience, hands‑on analytical testing skills (HPLC/UPLC, GC, dissolution), and strong communication abilities to deliver high‑quality results under regulatory requirements.