Senior Analytical Scientist

Accentuate Staffing; Durham (NC); On-site; USD 80,000 - 110,000; Full time

Job summary

A leading company in pharmaceutical manufacturing seeks a Senior Analytical Scientist to join their team. The successful candidate will oversee the development, validation, and transfer of analytical methodologies while ensuring compliance with GMP regulations. This direct hire opportunity offers competitive pay and the chance to work onsite in a collaborative environment.

Qualifications

• 6+ years in GMP-regulated industry with Bachelor's or 2+ years with Master's.
• Direct experience in pharmaceutical manufacturing or CDMO environment preferred.
• Proficient in analytical methodologies and laboratory software.

Responsibilities

• Develops, validates and transfers analytical methodologies.
• Solves diverse problems requiring data evaluation.
• Writes test procedures, protocols, and reports.

Skills

Method Development

Method Validation

HPLC

UV/Vis

CE

icIEF

Analytical Testing

Education

Bachelor’s degree

Master’s degree

Tools

Empower

MasterControl

Job description

Accentuate Staffing is partnering with a pharmaceutical manufacturer in search of a Senior Analytical Scientist to join their team. This is a direct hire opportunity, offering competitive pay, while working onsite. The ideal candidate has method development and method validation experience in a GMP-regulated, pharmaceutical manufacturing experience combined with the ability to perform HPLC, CE, icIEF, and UV/Vis based methodologies.

Responsibilities:

1. Develops, validates and transfers analytical methodology for analysis via HPLC , UV, CE and icIEF.
2. Executes reviews of solutions and wet chemical analyses and chromatography.
3. Understands the theoretical basis of both methods and experiments.
4. Solves problems of diverse scope in which analysis of data requires evaluation of identifiable factors.
5. Writes test procedures, protocols, and reports.

Requirements:

1. Bachelor’s degree and 6+ years of GMP-regulated industry experience or Master’s degree with 2+ years of GMP-regulated industry experience.
2. Direct experience in a pharmaceutical manufacturing or CDMO environment is highly preferred.
3. Experience performing HPLC, UV/Vis, CE, icIEF, analytical routine and non-routine testing.
4. Proficiency using laboratory software such as Empower and MasterControl.
5. Skilled performing method validations and method development.