CMC Operations Associate II - Analytical Programs

Kailera Therapeutics, Inc.; Waltham (MA); On-site; USD 78,000 - 95,000; Full time

Benefits offered by this job

Health insurance

401(k) match

Tuition reimbursement

Commuter benefits

Disability and life insurance

Annual bonus opportunities

Equity grants

Job summary

Kailera Therapeutics, Inc. is seeking an Associate II, CMC Operations to support analytical CMC program management across multiple development projects.

The role reports to the Associate Director, CMC Operations and collaborates with the CMC core team & cross-functional sub-teams to manage timelines and deliverables. This onsite, hub-based role in Waltham, MA expects 2-5 years in pharma development and a scientific background.

Qualifications

• 2-5 years of experience in pharmaceutical drug development and track record of success supporting multiple projects or programs simultaneously.
• Demonstrated creativity, problem solving and productivity.
• Experience working in interdisciplinary and cross-functional teams.
• Comfortable in a dynamic, fast-paced, entrepreneurial environment.

Responsibilities

• Participate in vendor meetings and track and manage analytical documents and deliverables.
• Support analytical CMC activities by tracking vendor progress and ensuring work aligns with contracts.
• Assist with CMC analytical program budget and alert teams of potential changes not captured in contracts.
• Maintain and update CMC tracking tools and escalate issues as needed.
• Assist in managing relationships and communication with external partners or service providers.

Skills

Pharmaceutical development

Cross-functional teamwork

Problem solving

Adaptability

Education

Scientific discipline preferred

Job description

Kailera Therapeutics, Inc. is seeking an Associate II, CMC Operations to support analytical CMC program management across multiple development projects.

The role reports to the Associate Director, CMC Operations and collaborates with the CMC core team & cross-functional sub-teams to manage timelines and deliverables. This onsite, hub-based role in Waltham, MA expects 2-5 years in pharma development and a scientific background.