Cell Therapy Manufacturing Compliance Expert (On-Site)

Cedent; Cambridge (MA); On-site; USD 70,000 - 90,000; Full time

Job summary

A biopharmaceutical company in Cambridge, MA is seeking a Compliance Specialist to support projects and manufacturing execution. The role involves coordinating manufacturing projects, leading investigations, and ensuring compliance with Good Manufacturing Practices. Ideal candidates should have a scientific degree and 2-5 years of relevant experience. Strong communication skills and teamwork capabilities are essential, along with familiarity with biopharmaceutical equipment. This position requires on-site work five days a week.

Qualifications

• 2-5 years of experience in a biopharmaceutical manufacturing environment.
• Knowledgeable of Current Good Manufacturing Practices and regulatory requirements.
• Ability to work a rotating holiday coverage schedule.

Responsibilities

• Coordinate and ensure successful completion of manufacturing projects.
• Lead investigations and provide troubleshooting for deviation reports.
• Implement corrective actions and assist in validation protocols.

Skills

Excellent communication skills

Organizational and planning skills

Familiarity with biopharmaceutical equipment

Ability to cooperate in a team environment

Education

BA/BS in a scientific discipline

Tools

Microsoft Office

OpCenter

ERP

Veeva

Job description

A biopharmaceutical company in Cambridge, MA is seeking a Compliance Specialist to support projects and manufacturing execution. The role involves coordinating manufacturing projects, leading investigations, and ensuring compliance with Good Manufacturing Practices. Ideal candidates should have a scientific degree and 2-5 years of relevant experience. Strong communication skills and teamwork capabilities are essential, along with familiarity with biopharmaceutical equipment. This position requires on-site work five days a week.