Manager, Manufacturing Operations (2nd Shift)

Scorpion Therapeutics; Boston (MA); On-site; USD 150,000 - 230,000; Full time

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

Role

Manage and lead cell therapy manufacturing operations, ensuring safe, compliant, and efficient cGMP production aligned with schedules and business goals.

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.

Requirements

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

Preferred

• cell therapy and aseptic processing experience, familiarity with POMS MES systems, and working in cGMP pharma settings.

High-value

• cell therapy modality, cGMP compliance, sterile/aseptic manufacturing, batch record review, GMP audits, and cross-functional collaboration.

Work setup

supporting 2nd shift operations with flexible scheduling, initial 90-day training, and on-site work in Cambridge and Leiden.