Senior Director, Raleigh

Indivior•Raleigh, NC

11d

About The Position

The Senior Director, Raleigh is a key leader in Indivior’s Manufacturing & Supply Organization, with full product, service, and cost accountability for manufacturing at the Raleigh, North Carolina site. The role provides leadership in customer service, manufacturing quality, site effectiveness, and efficiency to support organizational objectives and patient needs. It oversees stable, compliant, high-performing site operations and supports Sublocade manufacturing, future site expansion, engineering developments, and major IT changes. The position also has a future business-owner role for additional company-operated drug-product manufacturing sites. The role works across functions to meet site and Manufacturing & Supply Organization objectives; leads site emergency response; and partners with Site Quality and US Quality to maintain an excellent quality record and audit history with global regulatory bodies and the DEA. Domestic and international travel is required.

Requirements

University degree in Chemistry, Engineering, or Pharmacy.
At least 15 years of experience in the pharmaceutical or biotechnology industry.
At least 12 years of people-leadership experience.
Experience in results-driven pharmaceutical operations and manufacturing-site leadership.
Experience in aseptic pharmaceutical manufacturing, packaging, and particularly vials and pre-filled syringes.
Strong experience in Site Quality.
Ability to travel domestically and internationally.

Nice To Haves

Master’s degree preferred.
Experience in both large and small pharmaceutical or biotechnology companies.

Responsibilities

Maintain strict cost control and cost containment at the site.
Create stability and improve performance in ongoing site operations.
Build a site environment focused on performance, efficiency, compliance, continuous improvement, and exceptional quality standards.
Support staff retention and build operational capabilities for Sublocade.
Manage onsite engineering work to prepare the site for future expansion and engineering developments.
Oversee major planned IT changes at the site.
Work cross-functionally to meet annual objectives of the site and the Manufacturing & Supply Organization.
Take active leadership and ownership of site emergencies.
Maintain the highest levels of environmental, health, and safety (EH&S) at the site.
Analyze cost of goods and optimize materials and procurement, production scale, and commercial profit-margin feasibility.
Build manufacturing knowhow and identify opportunities to convert it into Indivior intellectual property.
Partner with Site Quality and US Quality to deliver and maintain an excellent site quality record and audit history with global regulatory bodies and the DEA.
Create and optimize site key performance indicators.
Monitor and optimize Sublocade manufacturing capacity at the site.
Serve as future business owner for additional company-operated drug-product manufacturing sites.

Benefits

Competitive paid time off plus company closure from December 24 through January 1.
Eligibility to participate in the company bonus program, based on company and individual performance.
Eligibility for a yearly grant through the Long-Term Incentive Plan.
401(k) and profit-sharing plan with company match.
U.S. Employee Stock Purchase Plan with a 15% discount.
Comprehensive medical, dental, vision, life, and disability coverage.
Health, dependent-care, and limited-purpose flexible spending accounts and HSA options.
Adoption assistance.
Tuition reimbursement.
Concierge and personal-assistance services.
Voluntary benefits including legal, pet insurance, and critical illness coverage.
Wellness programs, discounts, and other perks.