Senior Analytical Project Lead – QC & GMP

Rentschler Biopharma, Inc.; Milford (CT); On-site; USD 90,000 - 130,000; Full time

Job summary

Rentschler Biopharma in Milford, MA, is seeking an Analytical Project Coordinator to serve as the primary QC contact for the complete analytical methods portfolio on client projects. You will work with the project team, internal QC departments, and external laboratories to ensure timely, compliant data delivery.

You will coordinate development, production, and QC activities, prepare for client meetings, and support method development, validations, change controls, and lifecyle management of

Qualifications

• Masters degree with 5+ years in Analytical Process Sciences, Analytics, or PM in pharma/CDMO.
• Or Bachelor’s degree with 7+ years in analytical project management in pharma.
• Solid experience with GMP-compliant analytics.
• Strong written and verbal communication skills.

Responsibilities

• Serve as the primary QC contact for the analytical methods portfolio on client projects.
• Represent QC in client projects and coordinate with internal departments and external labs.
• Assess client needs, plan analytical work packages, and prepare client-facing presentations.
• Coordinate development, production, and QC timelines; support method development/validation.
• Assist with change controls, SOPs, investigations, and lifecycle management of analytical methods.

Skills

Project management

Analytical development

Communication

Quality mindset

Attention to detail

Education

Master's Degree in biochemistry/biotechnology

Bachelor's Degree in biochemistry/related field

Tools

Microsoft Office

Job description

Rentschler Biopharma in Milford, MA, is seeking an Analytical Project Coordinator to serve as the primary QC contact for the complete analytical methods portfolio on client projects. You will work with the project team, internal QC departments, and external laboratories to ensure timely, compliant data delivery.

You will coordinate development, production, and QC activities, prepare for client meetings, and support method development, validations, change controls, and lifecyle management of