Senior R&D GMP Quality Lead – Pharmaceutical Sciences

BioSpace; Lexington (MA); On-site; USD 111,800 - 175,670; Full time

Job summary

A leading biopharmaceutical company is seeking a Principal Manager for R&D GMP Pharmaceutical Sciences Quality. This role ensures quality oversight in drug development and compliance with cGMP regulations. With a focus on collaboration and independent decision-making, the ideal candidate will have a relevant degree and experience in the pharmaceutical industry. Strong problem-solving and communication skills are essential. This position is based in Lexington, MA and includes attractive compensation benefits.

Qualifications

• 5+ years of increasing responsibility in manufacturing, QC/QA, or compliance.
• Comprehensive understanding of international pharmaceutical regulations.
• Ability to mentor and guide team capabilities.

Responsibilities

• Oversee final release and disposition of Clinical Trial Material.
• Collaborate with partners to resolve quality events.
• Serve as GMP QA authority and provide strategic quality guidance.

Skills

Problem-solving skills

Communication skills

Attention to detail

Organizational skills

Education

Bachelor’s degree in a relevant scientific field

Advanced degree preferred

Job description

A leading biopharmaceutical company is seeking a Principal Manager for R&D GMP Pharmaceutical Sciences Quality. This role ensures quality oversight in drug development and compliance with cGMP regulations. With a focus on collaboration and independent decision-making, the ideal candidate will have a relevant degree and experience in the pharmaceutical industry. Strong problem-solving and communication skills are essential. This position is based in Lexington, MA and includes attractive compensation benefits.