Analytical Development Scientist, GMP Drug Analysis

Vertex Pharmaceuticals; Boston (MA); On-site; USD 103,000 - 154,000; Full time

Job summary

Vertex Pharmaceuticals is seeking a qualified analytical development professional to join our team in Boston, MA. You will perform analytical testing, data interpretation, and method validation in support of small molecule development programs, working with LC/LC–MS, GC, and KF techniques.

You will design experiments, troubleshoot issues, maintain electronic lab notebooks, and collaborate across cross-functional teams to drive project milestones and ensure GMP-compliant methods are in place.

Qualifications

• BS, MS or PhD in life or physical sciences with preference for analytical chemistry.
• Minimum experience: PhD 0–3 years or MS 3+ years or BS 6+ years in analytical development.
• Experience designing validation protocols following ICH and FDA guidelines.

Responsibilities

• Conduct analytical testing and data review with interpretation and presentation of complex data.
• Independently design and perform technically challenging experiments with reliability and detail.
• Support method validation and develop GMP-friendly methods as needed.
• Collaborate cross-functionally on development programs and maintain accurate electronic lab notebooks.

Skills

HPLC

GC

KF

Data interpretation

Education

Ph.D. in Analytical Chemistry or life/physical sciences

M.S. in Analytical Chemistry or life/physical sciences

B.S. in Analytical Chemistry or life/physical sciences

Tools

HPLC instrument

GC instrument

KF instrument

Job description

Vertex Pharmaceuticals is seeking a qualified analytical development professional to join our team in Boston, MA. You will perform analytical testing, data interpretation, and method validation in support of small molecule development programs, working with LC/LC–MS, GC, and KF techniques.

You will design experiments, troubleshoot issues, maintain electronic lab notebooks, and collaborate across cross-functional teams to drive project milestones and ensure GMP-compliant methods are in place.