Senior Analytical Scientist - Radiopharma Development

Apex Systems; Boston (MA); On-site; USD 145,000 - 165,000; Full time

Benefits offered by this job

Medical, dental, and vision insurance

401K with company match

Employee stock purchase program

Health Savings Account

Employee Assistance Program

Job summary

Apex Systems is seeking a Senior Scientist, Analytical Development based in Boston, MA, to drive analytical method development for innovative radiopharmaceutical therapies. In this role, you will lead efforts to ensure GMP readiness, working alongside cross-functional teams and external partners.

The ideal candidate holds a PhD in relevant fields with extensive experience in method development and has a strong understanding of regulatory compliance. Join us to make a meaningful impact in cancer patient therapies.

Qualifications

• 5+ years experience in analytical method development.
• Hands-on experience working with radioactive materials.
• Deep knowledge of cGMP and ICH/FDA guidelines.

Responsibilities

• Lead analytical method development to support GMP readiness.
• Design and execute analytical strategies for regulatory submissions.
• Ensure compliance with GMP, GLP, and data-integrity standards.

Skills

Analytical method development

Strong background in analytical method development and separation science

Project management

Technical writing

Collaboration and influence across functions

Education

PhD in chemistry, pharmaceutical sciences, or related field

MSc with 10+ years experience or BS with 12+ years

Tools

HPLC

LC-MS

TLC

GC

Chromatography software

LIMS

Microsoft Office

Job description

Apex Systems is seeking a Senior Scientist, Analytical Development based in Boston, MA, to drive analytical method development for innovative radiopharmaceutical therapies. In this role, you will lead efforts to ensure GMP readiness, working alongside cross-functional teams and external partners.

The ideal candidate holds a PhD in relevant fields with extensive experience in method development and has a strong understanding of regulatory compliance. Join us to make a meaningful impact in cancer patient therapies.