Manufacturing Supervisor

Scorpion Therapeutics; Brooklyn Park (MN); On-site; USD 85,000 - 105,000; Full time

Job summary

Scorpion Therapeutics in Brooklyn Park, MN seeks a Manufacturing Supervisor overseeing Upstream/Cell Culture in a cGMP biologics manufacturing facility. The role focuses on supervising personnel, ensuring SOP and cGMP adherence, and coordinating with support functions to keep manufacturing processes compliant and efficient.

Responsibilities include process monitoring, documentation, training, deviation handling and investigations, with collaboration across QC, Regulatory and QA as needed.

Qualifications

• Bachelor’s degree (preferred) or an associate degree with 4+ or 6+ years of GMP experience, respectively.
• High school diploma with 8+ years in GMP and supervisory experience.
• Strong knowledge of biologics manufacturing, equipment operation and troubleshooting.

Responsibilities

• Manage personnel and ensure adherence to SOPs and cGMP regulations.
• Monitor manufacturing processes, documentation, training, deviations and investigations.
• Coordinate with validation and facilities; troubleshoot equipment issues; develop team goals.

Skills

cGMP/GDP

MS Office

Education

Bachelor's degree

Associate degree

High school diploma

Job description

Role

Manufacturing Supervisor overseeing Upstream/Cell Culture in a cGMP Biologics manufacturing facility.

Responsibilities

Managing personnel, ensuring adherence to SOPs and cGMP regulations, monitoring manufacturing processes, documentation, training, and supporting deviations and investigations. The role involves coordinating with support functions like validation and facilities, troubleshooting equipment issues, and developing team goals.

Qualifications

Bachelor's (preferred) or associate degree with 4+ or 6+ years of GMP experience respectively, or high school diploma with 8+ years in GMP. Prior supervisory experience and strong knowledge of biologics manufacturing, including equipment operation and troubleshooting, are required.

Skills

cGMP/GDP application, scientific understanding of biologics, and proficiency in MS Office.

Cross-Functional Collaboration

May involve cross-functional collaboration with QC, Regulatory, QA, and Materials Management.

High-value specifics

Biologics manufacturing, upstream/cell culture, GMP compliance, deviation management, and process troubleshooting.

Location

Brooklyn Park, MN.

Travel

Not specified.