Analytical QC Project Lead for Biopharma

Rentschler Biopharma; Milford (MA); On-site; USD 90,000 - 120,000; Full time

Job summary

Rentschler Biopharma SE in Milford, MA seeks an Analytical Project Coordinator to serve as the primary QC contact for the analytical methods portfolio and to support client projects through QC collaboration across development, production and laboratories.

Responsibilities include planning analytical work packages, validating methods, and coordinating with internal/external teams while ensuring GMP-compliant analytics and timely information flow.

Qualifications

• Master's degree with 5+ years in Analytical Process Sciences or related field.
• Bachelor's degree with 7+ years in Analytical Process Sciences or related field.
• Solid experience in common biological and protein chemical analytical methods.
• Knowledge of GMP-compliant analytics.
• Strong written and verbal communication skills.

Responsibilities

• Serve as primary QC contact for the complete analytical methods portfolio and liaise with project teams and laboratories.
• Represent QC labs and ensure compliance with quality standards in client projects.
• Determine client needs for work packages and assess capabilities and capacity.
• Prepare for client meetings by consulting SMEs and generating presentations.
• Plan analytical work packages including method development, qualifications, validation, specs, sampling.
• Coordinate analytical support across development, production, and QC.

Skills

Effective communication

GMP knowledge

Analytical mindset

Project coordination

Education

Master's degree in biochemistry/biotechnology or related field

Bachelor's degree with 7+ years in Analytical Process Sciences or related field

Tools

Microsoft Office

Job description

Rentschler Biopharma SE in Milford, MA seeks an Analytical Project Coordinator to serve as the primary QC contact for the analytical methods portfolio and to support client projects through QC collaboration across development, production and laboratories.

Responsibilities include planning analytical work packages, validating methods, and coordinating with internal/external teams while ensuring GMP-compliant analytics and timely information flow.