GMP Cell Therapy Manufacturing Supervisor

Cellipont; Research Forest (TX); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

401(k) strong employer match

Tuition reimbursement

Employee referral bonuses

Flexible work schedules and PTO

Health & wellness coverage including宠物

Job summary

Cellipont Bioservices in Texas is seeking a Manufacturing Supervisor to lead aseptic manufacturing operations, ensuring compliant batch records and SOPs are followed. You will oversee staff, coordinate scheduling, and drive continuous improvement with cross‑functional teams.

The role requires a Life Sciences or Chemical Engineering degree, 5–7 years GMP exposure in cell therapy, prior leadership, and strong skills in documentation, GDP guidelines, and problem solving.

Qualifications

• Bachelor’s Degree in Life Sciences or Chemical Engineering.
• 5–7 years GMP manufacturing experience in cell therapy.
• 3 years leadership/management in GMP environment.
• Experience writing, executing and reviewing SOPs/MBRs.
• Proficient with GDP guidelines and compliant documentation.

Responsibilities

• Oversee and schedule manufacturing operations and personnel.
• Lead a team to identify issues and implement solutions.
• Train staff on batch records, scheduling, purchasing raw materials, setting up batches, and inventory management.
• Ensure batches meet established quality standards and GMP compliance.
• Conduct GMP batch reviews with QA and close‑out sessions.
• Provide updates to managers, clients, and project teams on production progress.
• Drive continuous improvement initiatives within the manufacturing team.
• Collaborate with cross‑functional groups to resolve issues and improve processes.

Skills

Leadership

GMP experience

SOP writing

Documentation

Data interpretation

Communication

Excel

Problem solving

Flexible hours

2nd shift

Education

Bachelor's Degree in Life Sciences or Chemical Engineering

Tools

Microsoft Word

Microsoft Excel

Job description

Cellipont Bioservices in Texas is seeking a Manufacturing Supervisor to lead aseptic manufacturing operations, ensuring compliant batch records and SOPs are followed. You will oversee staff, coordinate scheduling, and drive continuous improvement with cross‑functional teams.

The role requires a Life Sciences or Chemical Engineering degree, 5–7 years GMP exposure in cell therapy, prior leadership, and strong skills in documentation, GDP guidelines, and problem solving.