Cell Therapy Manufacturing Operations Lead — 2nd Shift (cGMP)

Scorpion Therapeutics

Boston (MA)

On-site

USD 150,000 - 230,000

Full time

4 days ago
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Benefits offered by this job

2nd shift
On-site Cambridge/Leiden
Flexible scheduling
90-day training

Job summary

Scorpion Therapeutics seeks an experienced Manufacturing Lead to manage cell therapy production in a cGMP environment, ensuring safe, compliant operations aligned with schedules and business goals. This on-site role covers Cambridge and Leiden with 2nd shift support after a 90-day training.

Responsibilities include overseeing daily manufacturing activities, leading staff and supervisors, managing equipment setup and cleaning, reviewing batch records for compliance, and collaborating with

Qualifications

  • Bachelor's degree in science, engineering, or related field; 4+ years in pharmaceutical manufacturing with leadership experience.
  • Knowledge of cGMP, process validation, and sterile manufacturing.
  • Experience managing teams in a regulated environment.

Responsibilities

  • Oversee daily manufacturing activities, lead and support supervisors and staff, manage equipment setup and cleaning, review batch documentation for compliance.
  • Collaborate with cross-functional teams on investigations and deviations, enforce GMP standards, maintain audit readiness, and drive continuous improvement.

Skills

Leadership
GMP knowledge
cGMP
Sterile manufacturing
Batch records
Cross-functional collaboration
Investigations & deviations
Audit readiness
Continuous improvement
Equipment setup
Cleaning

Education

Bachelor's degree in science/engineering/related field

Tools

POMS MES

Job description

Scorpion Therapeutics seeks an experienced Manufacturing Lead to manage cell therapy production in a cGMP environment, ensuring safe, compliant operations aligned with schedules and business goals. This on-site role covers Cambridge and Leiden with 2nd shift support after a 90-day training.

Responsibilities include overseeing daily manufacturing activities, leading staff and supervisors, managing equipment setup and cleaning, reviewing batch records for compliance, and collaborating with

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