Associate Director, CMC & Tech Operations (Remote)

Travere Therapeutics; Kansas City (MO); On-site; USD 150,000 - 195,000; Full time

Benefits offered by this job

Health benefits

Retirement plan

Paid time off

Life insurance

Job summary

Travere Therapeutics is seeking an experienced CMC leader to drive the development, execution and oversight of the CMC strategy for a diverse portfolio of small molecules. You will manage external CMOs, collaborate with Regulatory, Quality, Clinical and Supply Chain to mitigate risks and achieve milestones.

This on-site San Diego role requires 10% travel and a strong track record in cGMP manufacturing. You will also author and edit CMC sections for regulatory submissions, provide technical

Qualifications

• Demonstrated leadership in CMC across multiple areas.
• Experience with small molecules, peptides, or biologics is preferred.
• Strong knowledge of process validation and tech transfer.

Responsibilities

• Provide strategic and technical leadership for tech transfer, scale-up, validation, and cGMP manufacturing from Phase I-III.
• Oversee CMOs and external partners to ensure scope, quality, timelines and budget.
• Review regulatory filings and master batch records; ensure compliance with cGMP.
• Mentor teams and contribute to regulatory submissions as needed.
• Travel up to 10% domestically and internationally.

Skills

Leadership

CMO management

cGMP knowledge

Education

Bachelor's in Process/Chemical Eng or Life Sciences

Job description

Travere Therapeutics is seeking an experienced CMC leader to drive the development, execution and oversight of the CMC strategy for a diverse portfolio of small molecules. You will manage external CMOs, collaborate with Regulatory, Quality, Clinical and Supply Chain to mitigate risks and achieve milestones.

This on-site San Diego role requires 10% travel and a strong track record in cGMP manufacturing. You will also author and edit CMC sections for regulatory submissions, provide technical