Travere Therapeutics

Associate Director, Commercial Manufacturing & Packaging

Travere Therapeutics • $150K — $195K *
US-AnywhereRemote in San Diego, CA
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Process or Chemical Engineering, Life Sciences, or related discipline required.
  • 8+ years of progressive experience in pharmaceutical manufacturing and packaging activities required.
  • Experience with multiple dosage forms, especially oral solid dosage forms, is desired.

Responsibilities

  • Direct and coordinate manufacturing activities at CMOs to ensure uninterrupted supply of drug products.
  • Establish and maintain manufacturing schedules based on sales forecasts and assess capacity and risk.
  • Verify suitability and validation of processes at CMOs for drug production.
  • Provide troubleshooting support for internal and external project teams.
  • Maintain knowledge of US and EU GMPs and regulatory guidance for drug manufacturing and packaging.
  • Represent commercial manufacturing during CMO selection and qualification processes.
  • Author and edit technical reports related to manufacturing as needed.

Benefits

  • Premium health, financial, work-life and well-being offerings for eligible employees and dependents.
  • Wellness and employee support programs.
  • Life insurance and disability coverage.
  • Retirement plans with employer match.
  • Generous paid time off.
Full Job Description
Department:
106800 Technical Operations

Location:
San Diego, USA- Remote

Position Summary:

The Associate Director, Commercial Manufacturing is accountable for the strategy, oversight, and execution of commercial drug product manufacturing and packaging activities across Travere's external manufacturing network. This role leads manufacturing planning, CMO governance, process validation, technology transfer, operational performance, and supply-risk management to ensure a reliable, compliant, and uninterrupted supply of commercial products. The Associate Director partners with Supply Chain, Quality, Regulatory Affairs, Technical Operations, and Commercial stakeholders to translate business forecasts and product strategies into executable manufacturing plans and to provide senior management with recommendations regarding capacity, resources, risk, and external manufacturing strategy.

Responsibilities:
  • Direct and coordinate manufacturing activities at CMOs for commercial drug products to ensure uninterrupted market supply.
  • Establish and maintain manufacturing schedules based on internal sales forecasts and Sales & Operations Planning meeting decisions; assess capacity, inventory, and supply risks and lead the development of mitigation and contingency plans.
  • Verify suitability, qualification and validation of processes at Contract Manufacturing Organizations (CMO) for drug product.
  • Provide manufacturing support, troubleshooting, on internal and external project teams.
  • Maintains up-to-date knowledge of US and EU GMPs and other regulatory guidance applicable to pharmaceutical drug product manufacturing and packaging.
  • Represent commercial manufacturing for technical due diligence, CMO selection, qualification, contracting support, and manufacturing-network strategy.
  • Author/edit technical reports on a variety of manufacturing-related subjects as needed.
  • Assist management during regulatory inspections and internal, and external audits.
  • Assist with the development of CMC sections of regulatory submissions.
  • Additional duties assigned as needed.


Education/Experience Requirements:
  • Bachelor's degree in Process or Chemical Engineering, Life Sciences, or related discipline required. Equivalent combination of education and applicable job experience may be considered.
  • 8+ years of progressive experience directly leading pharmaceutical manufacturing and packaging shop floor activities including process troubleshooting and optimization activities required.
  • Manufacturing experience with multiple dosage forms desired, including oral solid dosage forms.


Additional Skills/Experience:
  • The ideal candidate will embody Travere's core values: Courage, Community Spirit, Patient Focus and Teamwork.
  • Driven, intelligent, passionate about making a difference for patients with rare diseases.
  • Expert knowledge in process validation and technology transfer procedures.
  • Successful record of creating and managing complex project plans, timelines, and budgets, and development of risk mitigation strategies.
  • Ability to adapt to modification and changes to project plans, demonstrating flexibility to implement new strategies and tactics to accommodate these changes.
  • Team player and strong interpersonal and organizational skills and excellent verbal and written communication skills.
  • Excellent decision-making and collaboration skills with strong attention to detail.
  • Ability to travel 10% domestically and internationally.
  • All positions have an essential job function to be able to perform face to face work with colleagues and/or onsite in San Diego. No role is expected to be 100% remote.


Total Rewards Offerings:
Travere provides comprehensive total rewards offerings that demonstrate our commitment as a diverse, equitable, people-centric, and pay-for-performance organization.

Benefits: Our benefits include premium health, financial, work-life and well-being offerings for eligible employees and dependents, wellness and employee support programs, life insurance, disability, retirement plans with employer match and generous paid time off.

Compensation: Our competitive compensation package includes a combination of both cash compensation (base pay and short-term incentive) and long-term incentive compensation (company stock), designed to recognize, retain, and reward employees.

Target Base Pay Range:
$150,000.00 - $195,000.00

*This information is current as of the date of this posting and may be modified in the future. Actual pay offered to a candidate will depend on a variety of factors including the candidate's experience, education, skills, and location.

Travere will accept applications on an ongoing basis until a candidate is selected for the position.

About Travere Therapeutics

Travere Therapeutics is a biotechnology company that develops treatments for rare diseases. The company's products are focused on the treatment of kidney diseases, including focal segmental glomerulosclerosis (FSGS) and Alport syndrome. Travere Therapeutics was founded in 1998 and is headquartered in Alameda, California.
Learn more about Travere Therapeutics
Size
300 employees
Market Cap
$1.2 billion
Industry
Net Income
-$169.4 million
5 Year Trend
+11.2%
Revenue
$198.3 million
NASDAQ

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