Stability Coordinator

Scorpion Therapeutics; Town of East Greenbush (NY); On-site; USD 70,000 - 110,000; Full time

Benefits offered by this job

Student Loan Paydown

Tuition Reimbursement

Family Care Benefits

Inclusion, Culture and Well-Being

Job summary

Scorpion Therapeutics is seeking a detail-oriented stability professional to coordinate with multiple departments, author stability protocols, and maintain data for regulatory submissions within GMP environments.

The role involves reviewing analytical data, maintaining stability chamber inventory, preparing samples, and ensuring compliance. A Life Sciences bachelor's degree and strong communication are essential; experience with databases and cross-functional teams is preferred.

Qualifications

• Bachelor's degree in Life Sciences or related field.
• Strong attention to detail in regulated data environments.
• Ability to work independently and as part of cross-functional teams.
• Clear written and verbal communication for protocols and data reporting.

Responsibilities

• Coordinate with other departments to identify materials for stability.
• Author stability protocols and secure approvals before studies begin.
• Review analytical data and centralize it in a database to support studies.
• Supply stability data for regulatory submissions.
• Share stability data with other departments on request.
• Maintain stability chamber inventory and monitor performance.
• Prepare samples for stability studies (aliquotting, labeling, distributing).
• Comply with GMP and other regulatory requirements.

Skills

Attention to detail

Independent work

Clear communication

Regulatory data handling

Education

Bachelor's degree in Life Sciences

Tools

Database systems

Job description

What You’ll Do

• Coordinate with other departments to identify materials that need to be placed on stability.
• Author stability protocols and secure necessary approvals before each study begins.
• Review analytical data and compile it into a central database to support ongoing studies.
• Supply stability data needed for the submission of regulatory documents.
• Share stability data with other departments upon request.
• Maintain stability chamber inventory and monitor chamber performance.
• Remove samples from chambers according to protocol pull schedules and submit them to the appropriate testing group.
• Prepare samples for stability studies (aliquotting, labeling, and distributing to the correct chamber).
• Comply with all pertinent regulatory agency requirements, including Good Manufacturing Practice (GMP) standards.

Must-haves

• Bachelor’s degree in Life Sciences or a related field.
• Strong attention to detail and comfort working with data in a regulated environment.
• Ability to work independently and as part of a cross-functional team.
• Clear written and verbal communication skills, especially for authoring protocols and reporting data.

Preferred

• Prior experience in a stability program, quality control, or analytical testing environment.
• Familiarity with GMP or other regulated laboratory settings.
• Experience with database systems used to compile and track scientific data.
• Exposure to supporting regulatory submissions or interacting with regulatory agencies.

Benefits

• Student Loan Paydown program & Tuition Reimbursement
• Family Care Benefits
• Inclusion, Culture and Well-Being programs (including physical & mental health)