Manager, Manufacturing Operations

Scorpion Therapeutics; Boston (MA); On-site; USD 120,000 - 165,000; Full time

Job summary

Scorpion Therapeutics seeks a Manager of Manufacturing Operations to oversee day-to-day activities at a cGMP Drug Product Facility, owning batch documentation and investigations. You will supervise staff, prioritize tasks, ensure compliance, and drive process improvements with cross-functional partners.

Expect collaboration with internal and external teams on maintenance and upgrades, with mentorship of team members.

Qualifications

• Bachelor's in science, engineering, or technical field.
• 4+ years industry experience including supervisory duties.
• Knowledge of cGMP, process validation, and pharmaceutical development.
• Proficiency in QbD, DoE, SPC, and data analysis.

Responsibilities

• Manage staff and day-to-day operations.
• Prioritize tasks and ensure compliance with cGMP.
• Author/review batch documentation and lead investigations.
• Implement process improvements and drive maintenance/upgrades with teams.
• Mentor and develop team members.

Skills

Supervisory experience

Data analysis

DoE

QbD

SPC

batch documentation

lead investigations

Education

Bachelor's in science/engineering/technical field

Tools

cGMP knowledge

Process validation

Pharmaceutical development

Job description

Role

Manager of Manufacturing Operations overseeing day-to-day activities at a cGMP Drug Product Facility.

Responsibilities

• manage staff
• prioritize tasks
• maintain compliance
• author/review batch documentation
• lead investigations
• implement process improvements
• collaborate with internal/external departments on maintenance and upgrades
• mentor team members.

Requirements

• Bachelor's in science, engineering, or technical field
• 4+ years industry experience including supervisory duties
• knowledge of cGMP, process validation, and pharmaceutical development
• proficiency in QbD, DoE, SPC, and data analysis

High Value

• drug manufacturing
• solid oral dosage forms
• process development
• scale-up
• late-phase clinical manufacturing
• validation
• and compliance.

Work Setup

on-site first shift with possible shift flexibility; training in Cambridge and Leiden; support for onboarding through early 2027.